Molecular targeted therapy has emerged as a promising treatment of Hepatocellular carcinoma (HCC). One potential target is the Src family Kinase (SFK). C-Src, a non-receptor tyrosine kinase is a critical link of multiple signal pathways that regulate proliferation, invasion, survival, metastasis, and angiogenesis. In this study, we evaluated the effects of a novel SFK inhibitor, dasatinib (BMS-354825), on SFK/FAK/p130CAS, PI3K/PTEN/Akt/mTOR, Ras/Raf/MAPK and Stats pathways in 9 HCC cell lines.
OSU-03012 sensitizes breast cancers to lapatinib-induced cell killing: a role...Enrique Moreno Gonzalez
Lapatinib is characterized as an ErbB1/ErbB2 dual inhibitor and has recently been approved for the treatment of metastatic breast cancer. In this study, we examined mechanisms
associated with enhancing the activity of lapatinib via combination with other therapies.
ADAR2 editing activity in newly diagnosed versus relapsed pediatric high-grad...Enrique Moreno Gonzalez
High-grade (WHO grade III and IV) astrocytomas are aggressive malignant brain tumors affecting humans with a high risk of recurrence in both children and adults. To date, limited information is available on the genetic and molecular alterations important in the onset and progression of pediatric high-grade astrocytomas and, even less, on the prognostic factors that influence long-term outcome in children with recurrence. A-to-I RNA editing is an essential post-transcriptional mechanism that can alter the nucleotide sequence of several RNAs and is
mediated by the ADAR enzymes. ADAR2 editing activity is particularly important in mammalian brain and is impaired in both adult and pediatric high-grade astrocytomas.
Moreover, we have recently shown that the recovered ADAR2 activity in high-grade astrocytomas inhibits in vivo tumor growth. The aim of the present study is to investigate whether changes may occur in ADAR2-mediated RNA editing profiles of relapsed highgrade astrocytomas compared to their respective specimens collected at diagnosis, in four pediatric patients.
CXCR7 is induced by hypoxia and mediates glioma cell migration towards SDF-1a...Enrique Moreno Gonzalez
Glioblastomas, the most common and malignant brain tumors of the central nervous system, exhibit high invasive capacity, which hinders effective therapy. Therefore, intense efforts aimed at improved therapeutics are ongoing to delineate the molecular mechanisms governing glioma cell migration and invasion.
Antioxidant-mediated up-regulation of OGG1 via NRF2 induction is associated ...Enrique Moreno Gonzalez
Estrogen metabolism-mediated oxidative stress is suggested to play an important role in estrogen-induced breast carcinogenesis. We have earlier demonstrated that antioxidants,
vitamin C (Vit C) and butylated hydroxyanisole (BHA) inhibit 17β-estradiol (E2)-mediated oxidative stress and oxidative DNA damage, and breast carcinogenesis in female August
Copenhagen Irish (ACI) rats. The objective of the present study was to characterize the mechanism by which above antioxidants prevent DNA damage during breast carcinogenesis.
Label-Free Quantitation and Mapping of the ErbB2 Tumor Receptor by Multiple P...AB SCIEX India
Label-Free Quantitation and Mapping of the ErbB2 Tumor Receptor by Multiple Protease Digestion with Data-Dependent (MS1) and Data-Independent (MS2) Acquisitions :
Mass spectrometry-based proteomics combined with
stable-isotope labeling or tagging is a powerful technique for large-scale quantitation and unbiased characterization of the proteome. Nonetheless, it is well known that unbiased discovery proteomics typically suffers from limited dynamic range and sampling efficiency, which can only be partially addressed by incorporating orthogonal fractionation steps.
Variant G6PD levels promote tumor cell proliferation or apoptosis via the STA...Enrique Moreno Gonzalez
Glucose-6-phosphate dehydrogenase (G6PD), elevated in tumor cells, catalyzes the first reaction in the pentose-phosphate pathway. The regulation mechanism of G6PD and pathological change in human melanoma growth remains unknown.
OSU-03012 sensitizes breast cancers to lapatinib-induced cell killing: a role...Enrique Moreno Gonzalez
Lapatinib is characterized as an ErbB1/ErbB2 dual inhibitor and has recently been approved for the treatment of metastatic breast cancer. In this study, we examined mechanisms
associated with enhancing the activity of lapatinib via combination with other therapies.
ADAR2 editing activity in newly diagnosed versus relapsed pediatric high-grad...Enrique Moreno Gonzalez
High-grade (WHO grade III and IV) astrocytomas are aggressive malignant brain tumors affecting humans with a high risk of recurrence in both children and adults. To date, limited information is available on the genetic and molecular alterations important in the onset and progression of pediatric high-grade astrocytomas and, even less, on the prognostic factors that influence long-term outcome in children with recurrence. A-to-I RNA editing is an essential post-transcriptional mechanism that can alter the nucleotide sequence of several RNAs and is
mediated by the ADAR enzymes. ADAR2 editing activity is particularly important in mammalian brain and is impaired in both adult and pediatric high-grade astrocytomas.
Moreover, we have recently shown that the recovered ADAR2 activity in high-grade astrocytomas inhibits in vivo tumor growth. The aim of the present study is to investigate whether changes may occur in ADAR2-mediated RNA editing profiles of relapsed highgrade astrocytomas compared to their respective specimens collected at diagnosis, in four pediatric patients.
CXCR7 is induced by hypoxia and mediates glioma cell migration towards SDF-1a...Enrique Moreno Gonzalez
Glioblastomas, the most common and malignant brain tumors of the central nervous system, exhibit high invasive capacity, which hinders effective therapy. Therefore, intense efforts aimed at improved therapeutics are ongoing to delineate the molecular mechanisms governing glioma cell migration and invasion.
Antioxidant-mediated up-regulation of OGG1 via NRF2 induction is associated ...Enrique Moreno Gonzalez
Estrogen metabolism-mediated oxidative stress is suggested to play an important role in estrogen-induced breast carcinogenesis. We have earlier demonstrated that antioxidants,
vitamin C (Vit C) and butylated hydroxyanisole (BHA) inhibit 17β-estradiol (E2)-mediated oxidative stress and oxidative DNA damage, and breast carcinogenesis in female August
Copenhagen Irish (ACI) rats. The objective of the present study was to characterize the mechanism by which above antioxidants prevent DNA damage during breast carcinogenesis.
Label-Free Quantitation and Mapping of the ErbB2 Tumor Receptor by Multiple P...AB SCIEX India
Label-Free Quantitation and Mapping of the ErbB2 Tumor Receptor by Multiple Protease Digestion with Data-Dependent (MS1) and Data-Independent (MS2) Acquisitions :
Mass spectrometry-based proteomics combined with
stable-isotope labeling or tagging is a powerful technique for large-scale quantitation and unbiased characterization of the proteome. Nonetheless, it is well known that unbiased discovery proteomics typically suffers from limited dynamic range and sampling efficiency, which can only be partially addressed by incorporating orthogonal fractionation steps.
Variant G6PD levels promote tumor cell proliferation or apoptosis via the STA...Enrique Moreno Gonzalez
Glucose-6-phosphate dehydrogenase (G6PD), elevated in tumor cells, catalyzes the first reaction in the pentose-phosphate pathway. The regulation mechanism of G6PD and pathological change in human melanoma growth remains unknown.
A new assay for measuring chromosome instability (CIN) and identification of...Enrique Moreno Gonzalez
Aneuploidy is a feature of most cancer cells that is often accompanied by an elevated rate of chromosome mis-segregation termed chromosome instability (CIN). While CIN can act as a driver of cancer genome evolution and tumor progression, recent findings point to the existence of a threshold level beyond which CIN becomes a barrier to tumor growth and therefore can be exploited therapeutically. Drugs known to increase CIN beyond the therapeutic threshold are currently few in number, and the clinical promise of targeting the
CIN phenotype warrants new screening efforts. However, none of the existing methods, including the in vitro micronuclei (MNi) assay, developed to quantify CIN, is entirely satisfactory.
DRUG INFORMATIONOF GILTERITINIB AND ITS EFFICACY IN REFRACTORY FLT3- MUTATED AMLPARUL UNIVERSITY
Acute myeloid leukemia is a malignancy of proliferative, abnormally, or poorly differentiated cells of the hematopoietic system,
characterized by genetic heterogeneity. FMS-like tyrosine kinase 3- internal tandem duplication remains one of the most frequently mutated
genes in acute myeloid leukemia, especially in those with normal cytogenetics. The FMS-like tyrosine kinase 3- internal tandem duplication
and FLT3 tyrosine kinase domain mutations are biomarkers for high-risk acute myeloid leukemia and are associated with drug resistance
and high risk of relapse. Various FLT3 inhibitors are in clinical development, including lestaurtinib, tandutinib, quizartinib, midostaurin,
gilteritinib, and crenolanib. Gilteritinib is a small molecule that inhibits multiple receptor tyrosine kinases that also act as FMS-like tyrosine
kinase 3. Gilteritinib, a next-generation tyrosine kinase inhibitor, is approved in several countries worldwide for the treatment of relapsed or
refractory acute myeloid leukemia in adults with FMS-like tyrosine kinase 3 mutations. Gilteritinib demonstrated the ability to inhibit FLT3
receptor signaling and production in cells exogenously expressing FLT3 including FLT3 internal tandem duplication and tyrosine kinase
domain mutations FLT3-D835Y and FLT3-ITD-D835Y, and it induced apoptosis in leukemic cells possessing FLT3 internal tandem
duplication. In conclusion, gilteritinib therapy led to higher percentages of patients with the response and longer survival than salvage
chemotherapy among patients with relapsed or refractory FLT3-mutated acute myeloid leukemia
A new assay for measuring chromosome instability (CIN) and identification of...Enrique Moreno Gonzalez
Aneuploidy is a feature of most cancer cells that is often accompanied by an elevated rate of chromosome mis-segregation termed chromosome instability (CIN). While CIN can act as a driver of cancer genome evolution and tumor progression, recent findings point to the existence of a threshold level beyond which CIN becomes a barrier to tumor growth and therefore can be exploited therapeutically. Drugs known to increase CIN beyond the therapeutic threshold are currently few in number, and the clinical promise of targeting the
CIN phenotype warrants new screening efforts. However, none of the existing methods, including the in vitro micronuclei (MNi) assay, developed to quantify CIN, is entirely satisfactory.
DRUG INFORMATIONOF GILTERITINIB AND ITS EFFICACY IN REFRACTORY FLT3- MUTATED AMLPARUL UNIVERSITY
Acute myeloid leukemia is a malignancy of proliferative, abnormally, or poorly differentiated cells of the hematopoietic system,
characterized by genetic heterogeneity. FMS-like tyrosine kinase 3- internal tandem duplication remains one of the most frequently mutated
genes in acute myeloid leukemia, especially in those with normal cytogenetics. The FMS-like tyrosine kinase 3- internal tandem duplication
and FLT3 tyrosine kinase domain mutations are biomarkers for high-risk acute myeloid leukemia and are associated with drug resistance
and high risk of relapse. Various FLT3 inhibitors are in clinical development, including lestaurtinib, tandutinib, quizartinib, midostaurin,
gilteritinib, and crenolanib. Gilteritinib is a small molecule that inhibits multiple receptor tyrosine kinases that also act as FMS-like tyrosine
kinase 3. Gilteritinib, a next-generation tyrosine kinase inhibitor, is approved in several countries worldwide for the treatment of relapsed or
refractory acute myeloid leukemia in adults with FMS-like tyrosine kinase 3 mutations. Gilteritinib demonstrated the ability to inhibit FLT3
receptor signaling and production in cells exogenously expressing FLT3 including FLT3 internal tandem duplication and tyrosine kinase
domain mutations FLT3-D835Y and FLT3-ITD-D835Y, and it induced apoptosis in leukemic cells possessing FLT3 internal tandem
duplication. In conclusion, gilteritinib therapy led to higher percentages of patients with the response and longer survival than salvage
chemotherapy among patients with relapsed or refractory FLT3-mutated acute myeloid leukemia
MOLECULAR BIOLOGY TOOLS FOR ENVIRONMENTAL MANAGEMENT and the principle behind the methodology, the methodology of the technique is described well in here...............
Circulating Biomarkers for Alzheimer's Disease: Neurodegenerative Disorders ...QIAGEN
Alzheimer's disease (AD) is a complex neurodegenerative disorder. Circulating miRNAs hold great promise in the discovery of non-invasive and novel biomarkers for AD diagnosis and prognosis. This slideshow presents the role of miRNAs in AD and details current progress in biomarker discovery. Various tools for pathway-focused and genome-wide miRNA expression profiling, miRNA functional studies and target identification are also included.
Von Bubnoff - LebensMUT Krebsinformationstag, 23 Juli 2011patvocates
Krebspatienteninformationstag von LebensMUT, 23.07.2011, Grosshadern bei München. Vortrag von Dr. von Bubnoff über Grundlagen der CML: Biologie und Therapie
Wie können Patienten zur Deutschen CML-Allianz beitragen?jangeissler
Was macht die Deutsche CML-Allianz? Was ist unsere Rolle als, Patienten in der Allianz? Wie könnt Ihr dazu beitragen?" Präsentiert von Jan Geissler, Leukaemie-Online.de und Prof. Andreas Hochhaus, Universitätsklinikum Jena, beim Leukaemie-Online-Treffen 2015 in München
Inhibition of glutathione by buthionine sulfoximine enhanced the anti-cancer ...Ashujit
Multiple myeloma (MM) is an incurable blood cancer. Melphalan is an alkylating agent given prior to stem cell transplantation to MM patients. Increased glutathione confers resistance to melphalan. This study investigate the effect of inhibition of glutathione by BSO in preclinical models of MM. Pretreatment with BSO enhanced the anti-cancer effect of melphalan in cell lines and animal models. BSO and melphalan combination was well tolerated by animals and enhanced the survival as compared to controls, BSO and melphalan alone. BSO enhanced depth and duration of responses induced by melphalan. In the combination group, majority of treated animals achieved complete response (CR) and more than 20% had maintained CR. Also, the survival of animals was doubled after combination treatment as compared to BSO or melphalan alone. Mechanistic investigation demonstrated that BSO enhanced melphalan induced DNA damage, caspase cleavage and apoptosis. The combination also achieved multi-logs of cells kills in nine human multiple myeloma cell lines and primary MM cells isolated from blood and bone marrows. Interestingly, the effect of BSO and melphalan combination was abolished when cells were treated with N-acetyl cysteine and sodium thiosulfate but not with vitamin C and vitamin E. This observation suggests that effect of BSO is primarily driven by its ability to deplete glutathione and therefore preventing melphalan detoxification. Together, this study provides framework for testing the combination in a Phase I trial.
Environment inside even a small tumor is characterized by total (anoxia) or partial oxygen deprivation, hypoxia. It has been shown that radiotherapy and some conventional chemotherapies may be less effective in hypoxia, and therefore it is important to investigate how different drugs act in different microenvironments. In this study we perform a large screening of the effects of 19 clinically used or experimental chemotherapeutic drugs on four different cell lines in conditions of normoxia, hypoxia and anoxia.
Equol enhances tamoxifen's anti-tumor activity by induction of caspase-mediat...Enrique Moreno Gonzalez
Soy phytoestrogens, such as daidzein and its metabolite equol, have been proposed to be
responsible for the low breast cancer rate in Asian women. Since the majority of estrogen
receptor positive breast cancer patients are treated with tamoxifen, the basic objective of this
study is to determine whether equol enhances tamoxifen’s anti-tumor effect, and to identify
the molecular mechanisms involved.
Involvement of Interleukin-6 induced PI3K/Akt/mTor pathway in the regulation ...eshaasini
Hepatocellular Carcinoma (HCC) is an invasive cancer. Alphafoetoprotein (AFP) is a diagnostic marker for HCC directly related to the disease agressivity. Telomerase, is expressed by 90% of HCC. PI3K/Akt/mTOR pathway wich is regulated by IL-6 is activated in the HCC. Our aim is to investigate the effect of IL-6 on AFP and telomerase secretion in HepG2/C3A and PLC/ PRF/5 cell lines.
Involvement of Interleukin-6 Induced PI3K/Akt/mTor Pathway in the Regulation ...semualkaira
Hepatocellular Carcinoma (HCC) is an invasive
cancer. Alphafoetoprotein (AFP) is a diagnostic marker for HCC
directly related to the disease agressivity. Télomérase, is expressed
by 90% of HCC. PI3K/Akt/mTOR pathway wich is regulated by
IL-6 is activated in the HCC. Our aim is to investigate the effect
of IL-6 on AFP and telomerase secretion in HepG2/C3A and PLC/
PRF/5 cell lines.
Involvement of Interleukin-6 induced PI3K/Akt/mTor pathway in the regulation ...semualkaira
Hepatocellular Carcinoma (HCC) is an invasive cancer. Alphafoetoprotein (AFP) is a diagnostic marker for HCC directly related to the disease agressivity. Telomerase, is expressed by 90% of HCC. PI3K/Akt/mTOR pathway wich is regulated by IL-6 is activated in the HCC. Our aim is to investigate the effect of IL-6 on AFP and telomerase secretion in HepG2/C3A and PLC/ PRF/5 cell lines.
Involvement of Interleukin-6 induced PI3K/Akt/mTor pathway in the regulation ...eshaasini
Hepatocellular Carcinoma (HCC) is an invasive cancer. Alphafoetoprotein (AFP) is a diagnostic marker for HCC directly related to the disease agressivity. Telomerase, is expressed by 90% of HCC. PI3K/Akt/mTOR pathway wich is regulated by IL-6 is activated in the HCC. Our aim is to investigate the effect of IL-6 on AFP and telomerase secretion in HepG2/C3A and PLC/ PRF/5 cell lines.
Involvement of Interleukin-6 induced PI3K/Akt/mTor pathway in the regulation ...semualkaira
Hepatocellular Carcinoma (HCC) is an invasive cancer. Alphafoetoprotein (AFP) is a diagnostic marker for HCC directly related to the disease agressivity. Telomerase, is expressed by 90% of HCC. PI3K/Akt/mTOR pathway wich is regulated by IL-6 is activated in the HCC. Our aim is to investigate the effect of IL-6 on AFP and telomerase secretion in HepG2/C3A and PLC/ PRF/5 cell lines.
Recently, a phase II clinical trial in hepatocellular carcinoma (HCC) has suggested that the combination of sorafenib and 5-fluorouracil (5-FU) is feasible and side effects are manageable. However, preclinical experimental data explaining the interaction mechanism(s) are lacking. Our objective is to investigate the anticancer efficacy and mechanism of combined sorafenib and 5-FU therapy in vitro in HCC cell lines MHCC97H and SMMC-7721.
IRF5 Promotes the Progression of Hepatocellular Carcinoma and is Regulated by...JohnJulie1
The IRF family of proteins involves in the tumor progression. However, but the functions of IRF5 in the tumorigenesis are largely unknown. Here, IRF5 was found to be up-regulated in hepatocellular carcinoma (HCC). Interfering with IRF5 inhibited the growth and tumorigenic ability of HCC cells.
IRF5 Promotes the Progression of Hepatocellular Carcinoma and is Regulated by...NainaAnon
The IRF family of proteins involves in the tumor progression. However, but the functions of IRF5 in the tumorigenesis are largely unknown. Here, IRF5 was found to be up-regulated in hepatocellular carcinoma (HCC). Interfering with IRF5 inhibited the growth and tumorigenic ability of HCC cells. When studying the molecular mechanism, it was found that TRIM35 interacted with IRF5, promoting the ubiquitination and degradation of IRF5. In the clinical specimens of HCC, TRIM35 was negatively correlated with the expression of IRF5. These observations reveal the oncogenic function of IRF5 in the progression of HCC, suggesting that IRF5 is a promising target for the therapy of HCC.
IRF5 Promotes the Progression of Hepatocellular Carcinoma and is Regulated by...daranisaha
The IRF family of proteins involves in the tumor progression. However, but the functions of IRF5 in the tumorigenesis are largely unknown. Here, IRF5 was found to be up-regulated in hepatocellular carcinoma (HCC). Interfering with IRF5 inhibited the growth and tumorigenic ability of HCC cells. When studying the molecular mechanism, it was found that TRIM35 interacted with IRF5, promoting the ubiquitination and degradation of IRF5. In the clinical specimens of HCC, TRIM35 was negatively correlated with the expression of IRF5. These observations reveal the oncogenic function of IRF5 in the progression of HCC, suggesting that IRF5 is a promising target for the therapy of HCC.
IRF5 Promotes the Progression of Hepatocellular Carcinoma and is Regulated by...eshaasini
The IRF family of proteins involves in the tumor progression. However, but the functions of IRF5 in the tumorigenesis are largely unknown. Here, IRF5 was found to be up-regulated in hepatocellular carcinoma (HCC). Interfering with IRF5 inhibited the growth and tumorigenic ability of HCC cells. When studying the molecular mechanism, it was found that TRIM35 interacted with IRF5, promoting the ubiquitination and degradation of IRF5. In the clinical specimens of HCC, TRIM35 was negatively correlated with the expression of IRF5. These observations reveal the oncogenic function of IRF5 in the progression of HCC, suggesting that IRF5 is a promising target for the therapy of HCC.
IRF5 Promotes the Progression of Hepatocellular Carcinoma and is Regulated by...semualkaira
The IRF family of proteins involves in the tumor progression. However, but the functions of IRF5 in the tumorigenesis are largely unknown. Here, IRF5 was found to be up-regulated in hepatocellular carcinoma (HCC). Interfering with IRF5 inhibited the growth and tumorigenic ability of HCC cells. When studying the molecular mechanism, it was found that TRIM35 interacted with IRF5, promoting the ubiquitination and degradation of IRF5. In the clinical specimens of HCC, TRIM35 was negatively correlated with the expression of IRF5. These observations reveal the oncogenic function of IRF5 in the progression of HCC, suggesting that IRF5 is a promising target for the therapy of HCC.
IRF5 Promotes the Progression of Hepatocellular Carcinoma and is Regulated by...semualkaira
The IRF family of proteins involves in the tumor progression. However, but the functions of IRF5 in the tumorigenesis are largely unknown. Here, IRF5 was found to be up-regulated in hepatocellular carcinoma (HCC). Interfering with IRF5 inhibited the growth and tumorigenic ability of HCC cells. When studying the molecular mechanism, it was found that TRIM35 interacted with IRF5, promoting the ubiquitination and degradation of IRF5. In the clinical specimens of HCC, TRIM35 was negatively correlated with the expression of IRF5. These observations reveal the oncogenic function of IRF5 in the progression of HCC, suggesting that IRF5 is a promising target for the therapy of HCC.
IRF5 Promotes the Progression of Hepatocellular Carcinoma and is Regulated by...semualkaira
The IRF family of proteins involves in the tumor progression. However, but the functions of IRF5 in the tumorigenesis are largely unknown. Here, IRF5 was found to be up-regulated in hepatocellular carcinoma (HCC). Interfering with IRF5 inhibited the growth and tumorigenic ability of HCC cells. When studying the molecular mechanism, it was found that TRIM35 interacted with IRF5, promoting the ubiquitination and degradation of IRF5. In the clinical specimens of HCC, TRIM35 was negatively correlated with the expression of IRF5. These observations reveal the oncogenic function of IRF5 in the progression of HCC, suggesting that IRF5 is a promising target for the therapy of HCC.
Frizzled-8 receptor is activated by the Wnt-2 ligand in non-small cell lung c...Enrique Moreno Gonzalez
Wnt-2 plays an oncogenic role in cancer, but which Frizzled receptor(s) mediates the Wnt-2 signaling pathway in lung cancer remains unclear. We sought to (1) identify and evaluate the activation of Wnt-2 signaling through Frizzled-8 in non-small cell lung cancer, and (2) test whether a novel expression construct dominant negative Wnt-2 (dnhWnt-2) reduces tumor growth in a colony formation assay and in a xenograft mouse model.
Similar to Molecular mechanisms of action and potential biomarkers of growth inhibition of dasatinib (BMS-354825) on hepatocellular carcinoma cells (20)
Incidence of pneumonia and risk factors among patients with head and neck can...Enrique Moreno Gonzalez
This study investigated the incidence and patient- and treatment-related risk factors related to pneumonia acquired during radiotherapy (PNRT) in head and neck cancer (HNC) patients.
Gene expression analysis of a Helicobacter pyloriinfected and high-salt diet-...Enrique Moreno Gonzalez
Helicobacter pylori (H. pylori) infection and excessive salt intake are known as important risk factors for stomach cancer in humans. However, interactions of these two factors with gene expression profiles during gastric carcinogenesis remain unclear. In the present study, we investigated the global gene expression associated with stomach carcinogenesis and prognosis of human gastric cancer using a mouse model.
Acute myeloid leukemia (AML) is a hematopoietic malignancy with a dismal outcome in the majority of cases. A detailed understanding of the genetic alterations and gene expression changes that contribute to its pathogenesis is important to improve prognostication, disease monitoring, and therapy. In this context, leukemia-associated misexpression of microRNAs (miRNAs) has been studied, but no coherent picture has emerged yet, thus warranting further investigations.
Differences in microRNA expression during tumor development in the transition...Enrique Moreno Gonzalez
The prostate is divided into three glandular zones, the peripheral zone (PZ), the transition zone (TZ), and the central zone. Most prostate tumors arise in the peripheral zone (70-75%) and in the transition zone (20-25%) while only 10% arise in the central zone. The aim of this study was to investigate if differences in miRNA expression could be a possible explanation for the difference in propensity of tumors in the zones of the prostate.
Multicentric and multifocal versus unifocal breast cancer: differences in the...Enrique Moreno Gonzalez
The aim of this study was to evaluate the expression of the cell adhesion-related glycoproteins MUC-1, β-catenin and E-cadherin in multicentric/multifocal breast cancer in comparison to unifocal disease in order to identify potential differences in the biology of these tumor types.
The life in sight application study (LISA): design of a randomized controlled...Enrique Moreno Gonzalez
It is widely recognized that spiritual care plays an important role in physical and psychosocial well-being of cancer patients, but there is little evidence based research on the effects of spiritual care. We will conduct a randomized controlled trial on spiritual care using a brief structured interview scheme supported by an e-application. The aim is to examine whether an assisted reflection on life events and ultimate life goals can improve quality of life of cancer patients.
Clinical and experimental studies regarding the expression and diagnostic val...Enrique Moreno Gonzalez
Carcinoembryonic antigen-related cell adhesion molecule 1 (CEACAM1) is a multifunctional Ig-like cell adhesion molecule that has a wide range of biological functions. According to previous reports, serum CEACAM1 is dysregulated in different malignant tumours and associated with tumour progression. However, the serum CEACAM1 expression in nonsmall-cell lung carcinomas (NSCLC) is unclear. The different expression ratio of CEACAM1-S and CEACAM1-L isoform has seldom been investigated in NSCLC. This research is intended to study the serum CEACAM1 and the ratio of CEACAM1-S/L isoforms in NSCLC.
Assessment of preoperative exercise capacity in hepatocellular carcinoma pati...Enrique Moreno Gonzalez
Cardiopulmonary exercise testing measures oxygen uptake at increasing levels of work and predicts cardiopulmonary performance under conditions of stress, such as after abdominal surgery. Dynamic assessment of preoperative exercise capacity may be a useful predictor of postoperative prognosis. This study examined the relationship between preoperative exercise capacity and event-free survival in hepatocellular carcinoma (HCC) patients with chronic liver injury who underwent hepatectomy.
Overexpression of YAP 1 contributes to progressive features and poor prognosi...Enrique Moreno Gonzalez
Yes-associated protein 1 (YAP 1), the nuclear effector of the Hippo pathway, is a key regulator of organ size and a candidate human oncogene in multiple tumors. However, the expression dynamics of YAP 1 in urothelial carcinoma of the bladder (UCB) and its clinical/prognostic significance are unclear.
Abnormal expression of Pygopus 2 correlates with a malignant phenotype in hum...Enrique Moreno Gonzalez
Pygopus 2 (Pygo2) is a Pygo family member and an important component of the Wnt signaling transcriptional complex. Despite this data, no clinical studies investigating Pygo2 expression in lung cancer have yet been reported.
Differentiation of irradiation and cetuximab induced skin reactions in patien...Enrique Moreno Gonzalez
In order to improve the clinical outcome of patients with locally advanced squamous cell carcinoma of the head and neck (LASCCHN) not being capable to receive platinum-based chemoradiation, radiotherapy can be intensified by addition of cetuximab, a monoclonal antibody that blocks the epidermal growth factor receptor (EGFR). The radioimmunotherapy with cetuximab is a feasible treatment option showing a favourable toxicity profile. The most frequent side effect of radiotherapy is radiation dermatitis, the most common side effect of treatment with cetuximab is acneiform rash. Incidence and severity of these frequent, often overlapping and sometimes limiting skin reactions, however, are not well explored. A clinical and molecular differentiation between radiogenic skin reactions and skin reactions caused by cetuximab which may correlate with outcome, have never been described before.
Cholestasis induces reversible accumulation of periplakin in mouse liverEnrique Moreno Gonzalez
Periplakin (PPL) is a rod-shaped cytolinker protein thought to connect cellular adhesion junctional complexes to cytoskeletal filaments. PPL serves as a structural component of the cornified envelope in the skin and interacts with various types of proteins in cultured cells; its level decreases dramatically during tumorigenic progression in human epithelial tissues. Despite these intriguing observations, the physiological roles of PPL, especially in noncutaneous tissues, are still largely unknown. Because we observed a marked fluctuation of PPL expression in mouse liver in association with the bile acid receptor farnesoid X receptor (FXR) and cholestasis, we sought to characterize the role of PPL in the liver and determine its contributions to the etiology and pathogenesis of cholestasis.
Functional p53 is required for rapid restoration of daunorubicin-induced lesi...Enrique Moreno Gonzalez
The tumour suppressor and transcription factor p53 is a major determinant of the therapeutic response to anthracyclines. In healthy tissue, p53 is also considered pivotal for side effects of anthracycline treatment such as lesions in haematopoietic tissues like the spleen. We used a Trp53null mouse to explore the significance of p53 in anthracycline (daunorubicin) induced lesions in the spleen.
Post-diagnosis hemoglobin change associates with overall survival of multiple...Enrique Moreno Gonzalez
Anemia refers to low hemoglobin (Hb) level and is a risk factor of cancer patient survival. The National Comprehensive Cancer Network recently suggested that post-diagnosis Hb change, regardless of baseline Hb level, indicates the potential presence of anemia. However, there is no epidemiological study evaluating whether Hb change has direct prognostic values for cancer patients at the population level.
Cost-effectiveness of MRI for breast cancer screening in BRCA1/2 mutation car...Enrique Moreno Gonzalez
Women with mutations in BRCA1 or BRCA2 are at high risk of developing breast cancer and, in British Columbia, Canada, are offered screening with both magnetic resonance imaging (MRI) and mammography to facilitate early detection. MRI is more sensitive than mammography but is more costly and produces more false positive results. The purpose of this study was to calculate the cost-effectiveness of MRI screening for breast cancer in BRCA1/2 mutation carriers in a Canadian setting.
Impaired mitochondrial beta-oxidation in patients with chronic hepatitis C: r...Enrique Moreno Gonzalez
Hepatic steatosis is often seen in patients with chronic hepatitis C (CH-C). It is still unclear whether these patients have an impaired mitochondrial β-oxidation. In this study we assessed mitochondrial β-oxidation in CH-C patients by investigating ketogenesis during fasting.
Intraepithelial lymphocyte distribution differs between the bulb and the seco...Enrique Moreno Gonzalez
Evaluation of intraepithelial duodenal lymphocytosis (IDL) is important in celiac disease (CD). There is no established cut-off value for increased number of IELs in the bulb. We therefore investigated the relation between IEL counts in the bulb and duodenal specimens in non-celiac subjects.
Sticky siRNAs targeting survivin and cyclin B1 exert an antitumoral effect on...Enrique Moreno Gonzalez
Melanoma represents one of the most aggressive and therapeutically challenging malignancies as it often gives rise to metastases and develops resistance to classical chemotherapeutic agents. Although diverse therapies have been generated, no major improvement of the patient prognosis has been noticed. One promising alternative to the conventional therapeutic approaches currently available is the inactivation of proteins essential for survival and/or progression of melanomas by means of RNA interference. Survivin and cyclin B1, both involved in cell survival and proliferation and frequently deregulated in human cancers, are good candidate target genes for siRNA mediated therapeutics.
Association between variations in the fat mass and obesity-associated gene an...Enrique Moreno Gonzalez
It is clear that genetic variations in the fat mass and obesity-associated (FTO) gene affect body mass index and the risk of obesity. Given the mounting evidence showing a positive association between obesity and pancreatic cancer, this study aimed to investigate the relation between variants in the FTO gene, obesity and pancreatic cancer risk.
The cysteinyl leukotriene 2 receptor contributes to all-trans retinoic acid-i...Enrique Moreno Gonzalez
Cysteinyl leukotrienes (CysLTs) are potent pro-inflammatory mediators that are increased in samples from patients with inflammatory bowel diseases (IBDs). Individuals with IBDs have enhanced susceptibility to colon carcinogenesis. In colorectal cancer, the balance between the pro-mitogenic cysteinyl leukotriene 1 receptor (CysLT1R) and the differentiation-promoting cysteinyl leukotriene 2 receptor (CysLT2R) is lost. Further, our previous data indicate that patients with high CysLT1R and low CysLT2R expression have a poor prognosis. In this study, we examined whether the balance between CysLT1R and CysLT2R could be restored by treatment with the cancer chemopreventive agent all-trans retinoic acid (ATRA).
Why You Should Replace Windows 11 with Nitrux Linux 3.5.0 for enhanced perfor...SOFTTECHHUB
The choice of an operating system plays a pivotal role in shaping our computing experience. For decades, Microsoft's Windows has dominated the market, offering a familiar and widely adopted platform for personal and professional use. However, as technological advancements continue to push the boundaries of innovation, alternative operating systems have emerged, challenging the status quo and offering users a fresh perspective on computing.
One such alternative that has garnered significant attention and acclaim is Nitrux Linux 3.5.0, a sleek, powerful, and user-friendly Linux distribution that promises to redefine the way we interact with our devices. With its focus on performance, security, and customization, Nitrux Linux presents a compelling case for those seeking to break free from the constraints of proprietary software and embrace the freedom and flexibility of open-source computing.
Pushing the limits of ePRTC: 100ns holdover for 100 daysAdtran
At WSTS 2024, Alon Stern explored the topic of parametric holdover and explained how recent research findings can be implemented in real-world PNT networks to achieve 100 nanoseconds of accuracy for up to 100 days.
Enchancing adoption of Open Source Libraries. A case study on Albumentations.AIVladimir Iglovikov, Ph.D.
Presented by Vladimir Iglovikov:
- https://www.linkedin.com/in/iglovikov/
- https://x.com/viglovikov
- https://www.instagram.com/ternaus/
This presentation delves into the journey of Albumentations.ai, a highly successful open-source library for data augmentation.
Created out of a necessity for superior performance in Kaggle competitions, Albumentations has grown to become a widely used tool among data scientists and machine learning practitioners.
This case study covers various aspects, including:
People: The contributors and community that have supported Albumentations.
Metrics: The success indicators such as downloads, daily active users, GitHub stars, and financial contributions.
Challenges: The hurdles in monetizing open-source projects and measuring user engagement.
Development Practices: Best practices for creating, maintaining, and scaling open-source libraries, including code hygiene, CI/CD, and fast iteration.
Community Building: Strategies for making adoption easy, iterating quickly, and fostering a vibrant, engaged community.
Marketing: Both online and offline marketing tactics, focusing on real, impactful interactions and collaborations.
Mental Health: Maintaining balance and not feeling pressured by user demands.
Key insights include the importance of automation, making the adoption process seamless, and leveraging offline interactions for marketing. The presentation also emphasizes the need for continuous small improvements and building a friendly, inclusive community that contributes to the project's growth.
Vladimir Iglovikov brings his extensive experience as a Kaggle Grandmaster, ex-Staff ML Engineer at Lyft, sharing valuable lessons and practical advice for anyone looking to enhance the adoption of their open-source projects.
Explore more about Albumentations and join the community at:
GitHub: https://github.com/albumentations-team/albumentations
Website: https://albumentations.ai/
LinkedIn: https://www.linkedin.com/company/100504475
Twitter: https://x.com/albumentations
Goodbye Windows 11: Make Way for Nitrux Linux 3.5.0!SOFTTECHHUB
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Essentials of Automations: The Art of Triggers and Actions in FMESafe Software
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Unlocking Productivity: Leveraging the Potential of Copilot in Microsoft 365, a presentation by Christoforos Vlachos, Senior Solutions Manager – Modern Workplace, Uni Systems
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However, this ease of use means that the subject of security in Kubernetes is often left for later, or even neglected. This exposes companies to significant risks.
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LF Energy Webinar: Electrical Grid Modelling and Simulation Through PowSyBl -...DanBrown980551
Do you want to learn how to model and simulate an electrical network from scratch in under an hour?
Then welcome to this PowSyBl workshop, hosted by Rte, the French Transmission System Operator (TSO)!
During the webinar, you will discover the PowSyBl ecosystem as well as handle and study an electrical network through an interactive Python notebook.
PowSyBl is an open source project hosted by LF Energy, which offers a comprehensive set of features for electrical grid modelling and simulation. Among other advanced features, PowSyBl provides:
- A fully editable and extendable library for grid component modelling;
- Visualization tools to display your network;
- Grid simulation tools, such as power flows, security analyses (with or without remedial actions) and sensitivity analyses;
The framework is mostly written in Java, with a Python binding so that Python developers can access PowSyBl functionalities as well.
What you will learn during the webinar:
- For beginners: discover PowSyBl's functionalities through a quick general presentation and the notebook, without needing any expert coding skills;
- For advanced developers: master the skills to efficiently apply PowSyBl functionalities to your real-world scenarios.
Removing Uninteresting Bytes in Software FuzzingAftab Hussain
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In this work, we equipped AFL, a popular fuzzer, with DIAR and examined two critical Linux libraries -- Libxml's xmllint, a tool for parsing xml documents, and Binutil's readelf, an essential debugging and security analysis command-line tool used to display detailed information about ELF (Executable and Linkable Format). Our preliminary results show that AFL+DIAR does not only discover new paths more quickly but also achieves higher coverage overall. This work thus showcases how starting with lean and optimized seeds can lead to faster, more comprehensive fuzzing campaigns -- and DIAR helps you find such seeds.
- These are slides of the talk given at IEEE International Conference on Software Testing Verification and Validation Workshop, ICSTW 2022.
GraphSummit Singapore | The Future of Agility: Supercharging Digital Transfor...Neo4j
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Epistemic Interaction - tuning interfaces to provide information for AI supportAlan Dix
Paper presented at SYNERGY workshop at AVI 2024, Genoa, Italy. 3rd June 2024
https://alandix.com/academic/papers/synergy2024-epistemic/
As machine learning integrates deeper into human-computer interactions, the concept of epistemic interaction emerges, aiming to refine these interactions to enhance system adaptability. This approach encourages minor, intentional adjustments in user behaviour to enrich the data available for system learning. This paper introduces epistemic interaction within the context of human-system communication, illustrating how deliberate interaction design can improve system understanding and adaptation. Through concrete examples, we demonstrate the potential of epistemic interaction to significantly advance human-computer interaction by leveraging intuitive human communication strategies to inform system design and functionality, offering a novel pathway for enriching user-system engagements.
Threats to mobile devices are more prevalent and increasing in scope and complexity. Users of mobile devices desire to take full advantage of the features
available on those devices, but many of the features provide convenience and capability but sacrifice security. This best practices guide outlines steps the users can take to better protect personal devices and information.
2. Molecular mechanisms of action and potential
biomarkers of growth inhibition of dasatinib (BMS-
354825) on hepatocellular carcinoma cells
Alex Y Chang1,2,*
Email: alexchang@imc.jhmi.edu
Miao Wang1
Email: wangmiao@imc.jhmi.edu
1
Johns Hopkins University, Baltimore, USA
2
Johns Hopkins Singapore International Medical Centre, 11 Jalan Tan Tock
Seng, Singapore 308433, Singapore
*
Corresponding author. Johns Hopkins Singapore International Medical Centre,
11 Jalan Tan Tock Seng, Singapore 308433, Singapore
Abstract
Background
Molecular targeted therapy has emerged as a promising treatment of Hepatocellular
carcinoma (HCC). One potential target is the Src family Kinase (SFK). C-Src, a non-receptor
tyrosine kinase is a critical link of multiple signal pathways that regulate proliferation,
invasion, survival, metastasis, and angiogenesis. In this study, we evaluated the effects of a
novel SFK inhibitor, dasatinib (BMS-354825), on SFK/FAK/p130CAS,
PI3K/PTEN/Akt/mTOR, Ras/Raf/MAPK and Stats pathways in 9 HCC cell lines.
Methods
Growth inhibition was assessed by MTS assay. EGFR, Src and downstream proteins FAK,
Akt, MAPK42/44, Stat3 expressions were measured by western blot. Cell adhesion,
migration and invasion were performed with and without dasatinib treatment.
Results
The IC50 of 9 cell lines ranged from 0.7 µM ~ 14.2 µM. In general the growth inhibition by
dasatinib was related to total Src (t-Src) and the ratio of activated Src (p-Src) to t-Src. There
was good correlation of the sensitivity to dasatinib and the inhibition level of p-Src, p-
FAK576/577 and p-Akt. No inhibition was found on Stat3 and MAPK42/44 in all cell lines.
The inhibition of cell adhesion, migration and invasion were correlated with p-FAK
inhibition.
3. Conclusion
Dasatinib inhibits the proliferation, adhesion, migration and invasion of HCC cells in vitro
via inhibiting of Src tyrosine kinase and affecting SFK/FAK and PI3K/PTEN/Akt, but not
Ras/Raf/MEK/ERK and JAK/Stat pathways. T-Src and p-Src/t-Src may be useful biomarkers
to select HCC patients for dasatinib treatment.
Keywords
Src kinase, Mechanism of inhibition, Dasatinib, Biomarker, Hepatocellular carcinoma
Background
Hepatocellular carcinoma (HCC) is one of the most common malignancies worldwide
accounting for 500,000 ~ 600,000 deaths per year [1]. The major obstacles in the treatment of
HCC are low resectable and high recurrence rates in patients with early disease and a poor
response to chemotherapy and radiation in advanced stage disease [2,3]. In addition, a
majority of HCC patients also have liver cirrhosis with poor liver functions and performance
status, thus limiting their ability to receive treatment. In fact, the existing conventional
chemotherapeutics are non-selective cytotoxic drugs with systemic side effects and no proven
survival benefit. Therefore, there is often no effective therapy that can be offered to these
patients [1,4]. In some series, up to 50% of patients with newly diagnosed HCC were only
given supportive or palliative therapy. There is an urgent need to develop novel treatments
for advanced HCC.
Targeted therapies that specifically inhibit pivotal molecular abnormalities have emerged as a
promising approach for various cancers, including HCC [5]. Sorafenib, a dual inhibitor of Raf
Kinase and VEGFR, is the only approved agent for treating advanced HCC. Sorafenib when
compared to placebo prolongs the survival modestly by 2 to 3 months. Therefore, more
efforts are necessary in the identification of new molecular targets to improve treatment
further. One potential target is found in the Src family Kinase (SFK). C-Src, a non-receptor
tyrosine kinase, has been found to be a critical component of multiple signaling pathways that
regulate proliferation, invasion, survival, metastasis, and angiogenesis [6,7]. To carry out
these activities, C-Src interacts with numerous cellular factors, including integrins, growth
factor receptors, G-protein coupled receptors and cytokine receptors to initiate their
downstream signaling cascades [8]. C-Src can cooperate with receptor kinases to signal
through downstream molecules, such as PI3K/PTEN/Akt, Ras/Raf/Mek1/2/Erk1/2 and Stats
[9-11]. C-Src also interacts with focal adhesion kinase (FAK), which plays an important role
in integrin signaling and is highly expressed in many tumor cells, including HCC [12].
Tyrosyl phosphorylation of FAK interacts with multiple cellular proteins to modulate cell
adhesion, migration and invasion [11].
Dasatinab (BMS-354825), a potent oral tyrosine Kinase inhibitor against the Src family
Kinases, BCR-ABL, platelet derived growth factor receptor and c-Kit has demonstrated
multiple effects on solid tumors and has been approved for use in patients with chronic
myelogenous leukemia refractory or intolerant to imatinib [13] and in patients with
Philadelphia chromosome-positive acute lymphoblastic leukemia [14]. Although there are
active research studies evaluating the molecular mechanisms of dasatinib on human solid
4. tumor cells such as prostate cancer, head and neck squamous cell carcinoma, non-small cell
lung cancer, breast cancer, but the true regulatory mechanisms are still not fully understood,
especially in HCC [15-21].
In this study, we hypothesize that dasatinib inhibits HCC by modulating
SFK/FAK/p130CAS, PI3K//PTEN/Akt/mTOR, Ras/Raf/MAPK and/or Stats signaling
pathways. The current investigation was undertaken to test this hypothesis.
Methods
Cell lines and cell culture
Human hepatocellular carcinoma (HCC) cell lines, HepG2, sk-Hep1, Hep3B were obtained
from ATCC, HLE, HLF, Huh-7, HT-17, PLC/PRF/6 and Li-7 were provided by Institute of
Molecular and Cell Biology of Singapore. All cell lines were cultured in Dulbecco’s
Modified Eagle Medium [high Glucose (4.5 g/L), with Sodium Pyruvate and L-glutamin]
(PAA Laboratories Cell Culture Products, Austria), containing 10% fatal bovine serum (FBS)
(Invitrogen, USA), 1% antibiotic with 100 IU/ml Penicillin and 100ug/ml Streptomycin
(Invitrogen, USA). Incubation condition was set at 37℃ in a humidified atmosphere of 95%
air and 5% CO2. The culture medium was changed 2 to 3 times a week and cells were
passaged using trypsin/EDTA (Invitrogen, USA).
Antibodies and reagents
Src rabbit monoclonal antibodies, β-actin, rabbit monoclonal antibodies against the phosphor-
Src(Tyr416), phosphor-Akt(Ser473), phosphor-MAK42/44(Thr202/Tyr204), phosphor-
Stat3(Tyr705), phosphor-FAK576/577 were from Cell Signaling Technologies, Canada.
Polyclonal antibody to phosphor-FAK861 was purchased from Invitrogen Corporation,
Canada. Polyclonal goat anti-rabbit immunoglobulins/HRP was from Dakocytomation,
Denmark. Recombinant human epidermal growth factor was purchased from Invitrogen
Corporation, USA. Dasatinib was obtained from Bristol-Myers Squibb, Princeton, USA.
Growth inhibition assay
Dasatinib was diluted in pure DMSO to obtain a stock solution of 10 mmol/L and stored in a
−80℃ freezer in aliquots. CellTiter 96 Aqueous Non-Radioaction cell proliferation Assay Kit
(Promega Corporation, USA) was used for growth inhibition assays. 4000–10,000 HCC cells
from 9 cell lines were plated in 96-well flat-bottomed plates and cultured for 24 hours (h).
Cells were exposed to serially diluted dasatinib in DMEM with 1%FBS, for an additional 72
hours. 20 µl MTS/PMS solution was added into each well containing 100 µl of the culture
medium. Then, the cells were incubated for 3 h at 37℃ before measurement of absorbance at
490 nm with a Benchmark Plus microplate spectrophotometer (Bio-RAD, USA). Absorbance
values were expressed as a percentage of that for untreated cells, and the concentration of
dasatinib resulting in 50% growth inhibition (IC50) was calculated for each cell line. As
reported by us previously, we arbitrarily defined the sensitive cell lines as having their IC50 ≤
1uM and the resistant cell lines IC50 ≥1uM [22].
5. EGF stimulation and dasatinib treatment
Briefly, approximately 2 × 105
cells were seeded into 6-well plates in serum containing
medium. After 24 h culture, cells undertook serum starvation for additional 24 h and then
were exposed to 10 ng/ml EGF (Millipore, USA) for PLC/PRF/6 cells and 200 ng/ml for sk-
hep1 cells for 5 min, 10 min, 15 min, 30 min, 1 hour. Finally the cells were harvested for
western blotting analysis.
For dasatinib inhibition study, serum-starved cells were treated with various concentrations of
dasatinib for 24 h prior to the addition of 20% FBS stimulation, and then were collected for
western blotting analysis. In order to show that this treatment would not affect cellular
viability, we selected sk-Hep1 and Huh-7 as the representative examples of the sensitive and
resistant cell lines to dasatinib for the following experiment: 8000 cells were seeded into 96-
well plate overnight, and then divided into 3 groups A, B and C before dasatinib treatment.
Group A was serum-starved for 24 h, group B and C were incubated in culture medium with
1% FBS and 10% FBS respectively. After another 24 h dasatinib treatment MTS assay was
used to determine the cell viability.
Protein extraction and Western blotting
The cells were lysed for protein extraction using M-PER mammalian protein extraction
reagent with protease inhibitor and phosphatase inhibitor (Thermo scientific, Pierce
Biotechnology, USA). The total protein concentration was measured by BCA kit (Pierce
Biotechnology, USA). Isolated proteins (35 µg/lane) were separated by 8% SDS-PAGE and
transferred to a nitrocellulose membrane by the iblot device (Invitrogen Corporation, CA).
The membranes were blocked with 5% BSA at room temperature for 1 h and then subjected
to immunoblots using primary antibodies at 4℃ overnight, followed by incubation with
secondary goat anti-rabbit IgG conjugated to horseradish peroxidase for 1 h at room
temperature. Labeled protein was visualized by chemiluminescence (Immobilon, Millipore
Corperation, USA) and exposure x-ray film (Kodak, USA), using β-actin expression as the
internal standard.
Cell adhesion, migration and invasion assay
Cells were pretreated with dasatinib (1 µM) for 24 h after being starved overnight at 37℃ in a
humidified incubator containing 5% CO2. Cell adhesion assay was performed using the cell
adhesion assay kit (Chemicon International, USA) by following the manufacturer
instructions. Briefly, 96-well plates were coated with different Extracellular Matrix (ECM)
proteins. Pretreated cells were re-suspended in assay buffer (Kit components) and seeded
(1.5x105
) in each well. Plates were then incubated for 2 h at 37℃ with 5% CO2. After
removing the non-adherent cells and washing by assay buffer, cells were fixed and stained for
5 minutes, after washing 3–5 times with deionized water, the cell-bonded stain was
solubilized and quantified with an ELASA plate reader (Benchmark Plus microplate
spectrophotometer, Bio-RAD, USA), at 560 nm.
Cell migration assays was done by using the cell migration assay kit (Chemicon International,
USA). Briefly, inserts with an 8 µm pore size polycarbonate membrane were utilized. 1.5 ×
105
cells were pretreated with dasatinib for 24 h and then seeded after washing off dasatinib
into the inserts. Same number of untreated cells was used as control. All the inserts were put
in the 24-well plate which was considered as the lower chamber, then DMEM with 10% FBS
6. as the chemo- attractant was supplied in each wells. The cells were allowed to incubate at
37℃ with 5% CO2 for 6 h and 16 h respectively. After that, cells in the inner surface of the
inserts were gently removed. Cells that had migrated through the polycarbonate membrane
were incubated with cell stain solution (kit components), then subsequently extracted and
detected on a standard microplate reader (Benchmark Plus microplate spectrophotometer,
Bio-RAD, USA), at 560 nm.
Cell invasion assay was processed by using the cell invasion assay kit (Chemicon
International, USA). A 24-well tissue culture plate with cell culture inserts which contained
an 8 µm pore size polycarbonate membrane was used. 1.5 × 105
testing cells in serum free
DMEM were plated into ECM coated insert, then DMEM with 10% FBS was placed in the
24-well plate as chemo attractants. After 48 h incubation, the cells were removed from the
inner surface of the insert using a cotton-tipped swab. The cells that invaded through the
ECM layer and clung to the bottom of the polycarbonate membrane were fixed and stained.
The number of migrating cells per insert was captured microscopically at 4× magnification.
Statistical analysis
All the experiments were repeated at least 3 times. Data are reported as means ± SD.
Correlation coefficient (r) was calculated by the Pearson product–moment correlation
coefficient, and statistical significance (p-value) was analyzed using t approximation. The
expression level of protein measured by western blot was analyzed by ImagJ software, p-
values were calculated using the Students t-test.
Results
Growth inhibition by dasatinib in 9 HCC cell lines
The growth inhibition of each cell line was quantified by IC50 of dasatinib which ranged from
0.7 µM ~ 14.2 µM. Dasatinib showed a dose-dependent inhibition in all 9 HCC cell lines, Sk-
Sep 1, Li-7, and PLC/PRF/6 were most sensitive with IC50 at or below 1 µM of dasatinib,
while Huh-7 was most resistant (Figure 1A).
Figure 1 Baseline protein expression as well as IC50 of dasatinib in HCC cell lines. A, 9
HCC cell lines were exposed to the dedicated concentrations of dasatinib for 72 hours, and
IC50 was tested by MTS. Results represent the mean (± SD) of three experiments. B and C,
cell lysates were prepared from untreated HCC cell lines and subjected to western blot
analysis with antibodies to p-Src416, t-Src, p-EGFR1068, t-EGFR and β-actin. D, the
expression ratio of p-Src416, P-EGFR1068, Src and EGFR to β-actin was quantified by
ImageJ software respectively. Results represented the mean (±SD) of three experiments.
Dasatinib inhibits Src activity and downstream signaling
The baseline levels of Src and activated Src (pY416-Src) were measured in 9 HCC cell lines
by western blotting (Figure 1B and 1C). Except HT-17 and Huh-7 the rest of the cell lines
showed significant correlation between growth inhibition by dasatinib (IC50) and the
expression level of total Src (t-Src) (p < 0.05, Figure 2A). The higher the expression of t-Src,
the more sensitive the HCC cell lines were to dasatinib. The average expression percent of p-
Src in t-Src (p-Src/t-Src) for sensitive cell lines was significantly lower than that of resistant
7. cell lines except for Huh-7 and HT-17 (p < 0.05). There was an extremely low expression of
p-Src at base line in Huh-7 cells. In the 6 resistant cell lines we demonstrated that the specific
activity of Src (the ratio of p-Src/t-Src) was significantly associated with the IC50 value of
dasatinib. The lower the ratio of activity of Src (p-Src/t-Src), the more resistant the HCC cell
lines to dasatinib (p = 0.001, Figure 2B). In 8 HCC cell lines the high levels of Src expression
were significantly associated with low levels of EGFR expression (p = 0.05, Figure 2C).
PLC/PRF/6 was the only cell line that expressed both high levels of t-Src and t-EGFR. The
expression level of phosphorylated EGFR (p-EGFR) was only detected in 4 cell lines
(PLC/PRF/6, Hep3B, HepG2 and HT-17).HT-17 showed the highest specific activity of
EGFR (p-EGFR/t-EGFR) (Figure 1B and 1C). Figure 1D showed the quantity of t-Src, p-Src,
t-EGFR and p-EGFR analyzed by software of ImageJ (Figure 1D). The cell viability of group
A, B and C did not show any significant difference by various concentration of dasatinib in
sk-Hep1 and Huh-7 cells (Figure 3A and 3B, p > 0.05). Although we showed serum affected
the cell proliferation (Figure 3C and 3D, p < 0.05), it couldn’t affect the response of HCC
cells to dasatinib.
Figure 2 Correlation between the growth inhibition by dasatinib and baseline protein
expression. A. The correlation between the growth inhibition by dasatinib and t-Src
expression in HCC cell lines. 7 out of 9 studied cell lines showed significant correlation (r =
−0.801, p = 0.03). B. The correlation between the IC50 of dasatinib and the ratio of p-Src/t-
Src in 6 dasatinib resistant HCC cell lines. (r = −0.96, p = 0.001). C. The correlation between
the expression level of Src and EGFR in 8 out of 9 HCC cell lines(r = −0.62, p = 0.05). All
the studied protein expression were measured by western blot and analyzed by ImageJ.
Figure 3 The comparison of cell viability with different treatment condition. Sk-Hep1
and Huh-7 cells were treated under three different conditions as described in methods.
Results represented the mean (±SD) of three experiments. There was no influence of cell
survival of sk-Hep1 (A) and Huh-7 (B) cells by dasatinib. Serum affected the cell
concentration of sk-Hep1 (C) and Huh-7 (D) cells without the influence by dasatinib
concentration.
The effects of dasatinib on Src and downstream targets were detected by western blotting in
dasatinib-treated cells (Figure 4). The expression ratio of individual phosphor-protein to β-
actin was quantified by ImageJ software (See Additional file 1). We analyzed the protein
inhibition level in HCC cells when treated with dasatinib at the dosage of 1uM. In general,
there was a significant correlation between the IC50 of dasatinib and the inhibition of p-Src
(7/9, p < 0.05, Figure 5A), p-Akt (7/9, p < 0.05, Figure 5B) and p-FAK576/577 (7/9, p <
0.01, Figure 5C) by dasatinib. In all 3 sensitive cell lines, sk-hep1, Li-7 and PLC/PRF/6, the
sensitivity to dasatinib was significantly correlated with p-Src and P-FAK576/577 inhibition
by dasatinib. 5 out of 9 HCC cell lines including all sensitive cell lines had a significant
correlation between p-Src inhibition and p-FAK576/577 inhibition by dasatinib (p < 0.05,
Figure 6A). P-Src inhibition and p-Akt inhibition by dasatinib were also showed significant
correlation in 5 HCC cell lines (p < 0.05, Figure 6B). We didn’t find any significant
inhibition of Stat3 and MAPK42/44 activities in all cell lines by dasatinib at the dosage of
1uM and below (Figure 4).
Figure 4 The effect of dasatinib in cell signalling. Western blot analysis with
phosphorylated Src, FAK, Stat3, Akt and MAPK in HCC cell lines after 24 hours treatment
of dasatinib. The cell lines were arranged according to their IC50 to dasatinib. The top three
were most sensitive, the bottom 3 were least sensitive.
8. Figure 5 Correlation between the IC50 of dasatinib and the inhibition on the activity of
Src, Akt, FAK. The inhibition levels of p-Src, p-Akt and p-FAK were measured when cells
were treated with dasatinib at the dosage of 1uM and analyzed by ImageJ software. To
analyze the correlation amongst the inhibition of different activated proteins by dasatinib, the
inhibition of activated protein is calculated by the following formula,
for example:
/
/
, D for dasatinib treatment, C for control. A, 7 out of 9 studied
HCC cell lines showed good correlation between IC50 and p-Src416 inhibition (r = 0.745, p =
0.03). B, 7 out of 9 studied HCC cell lines showed good correlation between IC50 and p-
Akt473 inhibition (r = 0.732, p = 0.03). C, 7 out of 9 studied HCC cell lines showed good
correlation between IC50 and P-FAK576/577 inhibition (r = 0.838, p = 0.01).
Figure 6 Correlation of the expression level between p-FAK, p-Akt and p-Src inhibition
after dasatinib treatment. The methods of measurement and calculation is the same as
Figure 5. A. 5 out of 9 HCC cell lines showed a good correlation between Src and FAK
inhibition by dasatinib (r = 0.843, p = 0.04). B. 5 out of 9 HCC cell lines showed a good
correlation between p-Src and p-Akt inhibition by dasatinib (r = 0.843, p = 0.04). The
inhibition levels of p-Src, p-Akt and p-FAK were measured when cells were treated with
dasatinib at the dosage of 1uM and analyzed by ImageJ software.
Individually, sk-Hep1, the most sensitive to dasatinib growth inhibition, showed only
moderate inhibition of p- Src, p-FAK576/577 and p-Akt by dasatinib at the dosage of 1uM. .
Even though dasatinib completely inhibited the expression of p-Src at 0.1uM in Li-7 cells, it
only moderately reduced the p-FAK576/577 activity without inhibiting p-Akt (Figure 3);
both sk-Hep1 and Li-7 expressed lower p-Src and p-Src/t-Src. It suggested that dasatinib may
affect other signal pathway and inhibiting other protein kinase or growth factors to regulate
cell growth in these two cell lines. PLC/PRF/6 was the only dasatinib sensitive cell line that
co-overexpressed t-Src and t-EGFR, higher baseline expression of p-Src and lower p-Src/t-
Src. In order to investigate whether dasatinib would affect EGFR signaling pathway, the
activity of EGFR was tested too. The p-Src, p-FAK576/577, p-FAK861 and p-Akt were
significantly inhibited by dasatinib at 0.1uM, p-EGFR1068 was inhibited at 10uM. No
inhibition of t-Src expression by dasatinib at all (Figures 4 and 7). It appeared at lower
concentration of dasatinib (0.01uM) there was a slight increase of p-Src. The mechanism of
such difference is unknown. However, the ratio of p-Src/t-Src of control vs dasatinib
treatment (0.01um) did not have any significant difference (p > 0.05).
Figure 7 Effect of dasatinib on PLC/PRF/6 cell signaling. Total Src and p-Src, p-EGFR
expression after dasatinib treatment in PLC/PRF/6 cell line were shown. P-Src/t-Src was
quantified by ImageJ software. * p < 0.05 as compared with the control (student’s t-test).
Huh-7 was the least sensitive to dasatinib and very little level of p-Src was detected before
dasatinib treatment but inhibition of p-Src can be demonstrated by dasatinib. In this cell line,
dasatinib not only could not reduce p-FAK at both 576/577 and 861 sites, but also increased
the level of them (Figure 4) suggesting Src dependant signaling pathway is not crucial in the
regulation of oncogenic processes for Huh-7 cells.
HT-17 is one of the most resistant cell lines to dasatinib, but is sensitive to gefitinib [22]. It
showed highest activity of EGFR at baseline. Even though dasatinib was able to inhibit p-
Src416 at the lower dosage (1uM), but did not reduce p-Akt473 and P-MAPK42/44. These
9. results indicated that the cell growth of HT-17 was most likely dependant on EGFR signal
pathway.
Figure 8 showed that the response of phosphorylated proteins to EGF stimulation varied in
different cell lines. P-Src can be activated by EGF (10 ng/ml) in PLC/PRF/6 (Figure 8A) but
not in sk-Hep1 (Figure 8B). p-FAK 576/577, 861 can be activated by EGF in both cell lines.
It suggested that FAK may be activated by other molecules such as the subunit PI3K p85,
phospholipase Cr and Grb7 in sk-Hep1 cells [11].
Figure 8 The effect of EGF stimulation on phosphorylated protein expression.
PLC/PRF/6 cells were stimulated with 10 ng/ml EGF for the indicated times, lysed and
analyzed by western blotting (A). Sk-Hep1 cells were stimulated with 200 ng/ml EGF for the
indicated times, lysed and analyzed by western bloting with the indicated antibodies (C). The
expression ratio of phosphorylated protein to β-actin was quantified by ImageJ software
respectively. Results represented the mean (±SD) of three experiments. * p < 0.05 as
compared with the control (student’s t-test) (B and D).
Dasatinib affects adhesion, migration and invasion of HCC cells
There was a strong correlation between the p-FAK inhibition and cell adhesion, migration
and invasion. After 24 h pretreatment, dasatinib significantly reduced adhesion of both sk-
Hep1(p < 0.01) and PLC/PRF/6 (p < 0.001) on various ECM proteins (collagen I, collagen II,
collagen IV, fibronectin, laminin, tenascin, vitronectin) with the range of inhibition from 25%
to 82%, and the reduction percentages by dasatinib showed a similar pattern on both cell
lines. However, in the most resistant cell line, Huh-7, the adhesion was significantly
increased from 13% to 50% by dasatinib at the dose of 1uM (Figure 9, p < 0.01).
Figure 9 The effect of dasatinib on cell adhesion in HCC cell lines (A, B, C). Pretreatment
for 24 hours, dasatinib inhibited adhesion of sk-Hep1 and PLC/PRF/6 cells on ECM protein
(A, B), but increased the adhesion of Huh-7 cells(C). ** p < 0.01 as compared with the
control (student’s t-test).
Dasatinib significantly reduced sk-Hep1 cells migration 6 h after removal from media (70%
reduction as compared to control) (p < 0.001) but the inhibition of migration at 16 h was only
20% (Figure 10B). However, it reduced PLC/PRF/6 migration by 71% significantly at 16 h (p
< 0.001). Again, Huh-7 cells migration was increased 50% by dasatinib (p < 0.001) (Figure
10A).
Figure 10 The effect of dasatinib on cell migration in HCC cell lines. A, dasatinib pre-
treatment for 24 hours inhibited migration of sk-Hep1, PLC/PRF/6, but increased migration
of Huh-7 cells. B, same test method as A, dasatinib inhibition on sk-hep1 cells 6 h and 16 h
after removing dasatinib from media. The inhibitory effect was stronger at 6 h than that at 16
h. ** p < 0.01 and *** p < 0.001 as compared with the control (student’s t-test).
Dasatinib significantly inhibited the invasion on ECM in sk-Hep1 cells (Figure 11, p <
0.001). Our results did not show any invasion inhibition by dasatinib in PLC/PRF/6 and Huh-
7, however, PLC/PRF/6 and huh-7 were not invasive even in the absence of dasatinib.
10. Figure 11 Effect of dasatinib on cell invasion. Invasive Sk-Hep1 HCC cells were captured
in the polycarbonate membrane without (A) and with (B) the treatment of dasatinib at 1uM.
Images were taken under invert light microscope (magnification: 100×). Images (C) and (D)
were captured under high-power microscope (magnification: 600×). The cell numbers of at
least 6 fields in each image were counted under microscope (magnification: 200×). The
percentages of cell invasion were calculated (E). 3 independent experiments were carried out
in duplicate. *** p < 0.001 as compared with the control (student’s t-test).
Discussion
In this report, we first demonstrated the heterogeneous sensitivity of 9 HCC cell lines to
dasatinib in vitro as shown by their IC50 values. Our study also showed that the growth
inhibition by dasatinib was correlated with t-Src in 7/9 cell lines and the p-Src/t-Src ratios
were significantly lower in sensitive cells than resistant cells in the same 7/9 cell lines. In 6
resistant cell lines the growth inhibition by dasatinib was related to specific activity of Src
protein by p-Src/t-Src ratio. With the exception of PLC/PRF/6, there was an inverse
correlation between t-Src and t-EGFR. Song et al. showed that dasatinib treatment resulted in
apoptosis in gefitinib-sensitive EGFR mutant lung cancer cells in-vitro [21]. Their findings
were also confirmed by other investigators recently [23,24]. Our results showed even in
gefitinib resistant HCC cell lines [22], some were still sensitive to dasatinib. There was also a
co-overexpression with Src and members of EGFR family in breast cancer [25]. Our findings
that EGFR expression influenced the response of HCC cells to dasatinib further strengthened
the notion that a unique cross-talk mechanism might exist between Src family and EGFR
family tyrosine kinases in hepatocarcinogenesis. These two TK signaling pathways may
complement each other in the oncogenic process and development of resistance to treatment
of either pathway. Our results suggested combination of inhibitors of both pathways may
yield better results, as we have shown synergistic interaction between dasatinib and gefitinib
in HCC cells on our previous study [22]. The preliminary study of dasatinib and erlotinib (an
EGFR TKI) combination in 29 evaluable patients with recurrent or metastatic non-small cell
lung cancer showed 2 partial response and 62% disease control rate [26]. More studies are
needed to explore the optimal combination and the right clinical settings.
Baseline t-Src and specific Src activity (p-Src/t-Src) may be used as useful predictive
biomarkers for selecting dasatinib treatment in HCC patients. We also showed in most of cell
lines, dasatinib suppressed the expression of p-Src, p-FAK and p-Akt which correlated with
the level of growth inhibition. So the inhibitory response of p-Src, p-FAK and p-Akt to
dasatinib may also provide guidance for predicting response, although they were more
variable than baseline t-Src. Significant correlation between IC50 and expression of t-Src
could be shown in majorities of cell lines, especially in gefitinib resistant cell lines. However,
there were exceptions, such as Huh-7 cells, Src-dependant signal pathway was not an
important determinant of cell proliferation, motility and invasion in Huh-7 cells which was
resistant to dasatinib but showed p-Src inhibition by dasatinib. Interestingly, we found that
high ratio of p-Src/t-Src was significantly associated with less resistant to dasatinib in all 6
dasatinib resistant cell lines. This implied that the mechanism of action of dasatinib in
sensitive cell lines may be different from that of resistant cell lines. In addition, there were
differences among other cell lines in the inhibition of p-Src, p-FAK, p-Akt, cell adhesion,
migration and invasion by dasatinib. Thus, we demonstrated the heterogeneity of HCC tumor
biology and the need for individualized treatment. Biomarkers may provide guidance for
selecting right treatment for the right patient. It will require prospective studies to validate
11. our findings. In the study of combination of dasatinib and erlotinib in patients with advanced
NSCLC, reduction of vascular endothelial growth factor (VEGF) was correlated with disease
control [26]. However, a phase II study of single agent dasatinib in advanced NSCLC showed
that neither activation of SFK nor EGFR and Kras mutations in tumor tissue predicted
response to dasatinib [27]. No clinical results are available yet from studying dasatinib in
advanced HCC patients.
Src interacts with FAK to play a key role in tumor cell migration and invasion. Upon
intergrin engagement or stimulation of EGF or PDGF receptors, FAK autophosphorylates at
pTyr397, creating a high affinity binding site for Src, the association between Src and FAK
resulted in activation of Src and phosphorylation of FAK at Tyr 576, 577, 861 and 925. The
Src/FAK complex phosphorylated a number of other focal adhesion proteins and activated
other intra cellular signaling pathway [28]. This interaction between Src and FAK has been
shown to control both cell motility and invasion [11]. Regarding our results, in 56% (5/9)
studied HCC cell lines, dasatinib inhibits the activity of Src to reduce phosphorylation of
FAK. Inhibition of FAK at Tyr576/577 was strongly correlated with HCC cell adhesion,
migration and invasion. For 78% (7/9) of studied HCC cell lines, reduction of activated
FAK576/577 was significantly correlated with the dasatinib sensitivity. Thus the SFK/FAK
signaling pathway plays an important role in cell adhesion, migration and invasion. Inhibition
of this pathway is one of the mechanisms of action of dasatinib. In MDA-MB-231 human
metastatic breast cells, dasatinib also showed the inhibition of cell proliferation, migration
and invasion, as well as the inhibition of Src, Fak (Y925), paxillin, caveolin-1 and p130Cas
activation [29]. Furthermore, conditional expression of SrcDN in MCF7 human breast cancer
cells reduces adhesion, migration and spreading. Because expression of SrcDN alters the
shape of MCF7 cells, immunofluorescence confocal analyses showed concentrated focal
adhesion proteins. However, the adhesion of cells was reduced [30]. In contrast, the most
resistant HCC cell line Huh-7 expresses escalated levels of activated FAK576/577 and
increases cell adhesion and migration after dasatinib treatment. A previous study reported
that increased cell adhesion, migration occured at the same time upon treatment with
prostaglandin E2by mediating FAK/paxillin/Erk2 signal pathway in the same HCC cell line
(Huh-7) [31]. The mechanism of dasatinib induced increases of cell adhesion, migration in
Huh-7 cells need further investigation. However, the nature of cell origin may determine
specific cellular responses and the activated FAK576/577 may be the factor contributing to
drug resistance.
Our study also revealed that FAK can be activated by EGF in HCC cell lines. In PLC/PRF/6
cell line, Src and FAK can be activated simultaneously by EGF, and completely inhibited by
dasatinib. In view of this result, dasatinib may directly inhibit the complete activation of FAK
through reducing the activity of Src TK. For sk-Hep1 cell line, EGF could not activate Src,
but dasatinib could also reduce the activity of FAK, indicating dasatinib may interplay with
other molecules to block the phosphorylation of FAK, and therefore inhibit the motility and
invasion of HCC cells.
The activated PI3K/PTEN/Akt/mTOR pathway has emerged as a novel contributor to HCC
tumor development [12]. 56% (5/9) of our studied HCC cell lines showed the inhibition of
Src activity by dasatinib also induced inhibition of p-Akt. It suggested that activated Src
might trigger PI3K pathway to activate Akt, which regulated multiple cellular proteins in cell
proliferation, apoptosis, metastasis and angiogenesis. In PLC/PRF/6 cell line, complete
inhibition of activated Src by dasatinib at the dosage of 0.1 uM, not only induced the
inhibition of Akt activity at the same dosage, but also induced the inhibition of p-EGFR at
12. Tyr1068 at higher dosage of 10uM (Figure 6). These findings indicated that EGFR may be a
direct target of dasatinib or an indirect target secondary to Src inhibition [8,11].
Our data showed little inhibition of p-Stat3, and p-MAKP 42/44 by dasatinib in all HCC cell
lines except at high concentration. Activation of Stat3 by altered Janus-activated Kinase-Stat3
binding has been reported as a potential mechanism of resistance to Src inhibition [32] and
should be a focus of future research on mechanisms of dasatinib resistance. In the resistant
Huh-7 cells, p-Stat3 expression was not different from sensitive cell lines, suggesting Stat3
may not play an important role in this cell line. Dasatinib was synergistic with oxaliplatin
against colon carcinoma cells and with cisplatin against NSCLC cells [33,34]. It was also
synergistic with gefitinib, bravinib, BMS-690514, BMS-536924 or ixabepilone as shown in
our previous studies [22]. In the future, it may be necessary to perform genomic and
proteomic evaluation of each patient to determine resistance patterns as shown by Li et al.
that dasatinib had nearly 40 distinct kinase targets [35,36].
Conclusions
Dasatinib inhibits the proliferation, adhesion, migration and invasion of HCC cells in vitro
via inhibiting Src and affecting SFK/FAK and PI3K/PTEN/Akt signaling pathways, but not
Ras/Raf/MEK/ERK and JAK/Stats pathways. Apart from Src, dasatinib may also inhibit
other tyrosine kinase protein or growth factor receptors in HCC cells. In general the growth
inhibition by dasatinib was related t-Src and the ratio of p-Src/t-Src. T-Src and p-Src/t-Src
may be useful biomarkers to select HCC patients for dasatinib treatment in the future. This is
consistent with the notion that the Src family Kinases cooperate with multiple receptor
tyrosine Kinases to modulate signaling cross talk and promoting proliferation, adhesion,
migration and invasion. Furthermore, dasatinib could be an attractive agent for combination
therapies such as combining with EGFR TKI or chemotherapy to exploit potential synergistic
interaction. Hence, further laboratory and translational researches are warranted to investigate
the role of dasatinib or other Src inhibitor in HCC.
Competing interest
Alex Y. Chang serves as a member of advisory committees of: Eli Lilly, Astella Pharma Inc.,
Eisai Limited, Bristol Myers Squibb Company, Agennix Inc. and received Research funding
from Astella Pharma Inc., Eisai Limited, Bristol Myers Squibb Company, Roche, Agennix
Inc. for conducting clinical trials.
Authors’ contributions
Study conception and design: AYC Performing tests: WM Analysis and interpretation: AYC,
WM Drafting manuscript: AYC, WM. Both authors read and approved the final manuscript.
Acknowledgements
The study was supported in part from a grant by Bristol-Myers Squibb Company and the
research fund of Johns Hopkins Singapore. All the experiments were carried out in the
Department of Urology Research Lab and Department of Clinical Research of Singapore
General Hospital.
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Additional file
Additional_file_1 as XLSX
Additional file 1 Densitometric quantitation of the blots of Figure 4. The expression ratio of
phosphorylated protein to β-actin was quantified by ImageJ software respectively. Results
represented the mean (±SD) of three experiments. * p < 0.05 as compared with the control
(student’s t-test).
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:
T
e n a s c
i
n
V
N
: V
i
t
r
o n e c t
i
n
N
e g :
N
e g t
i v
e
A . s k 0 H e p 1
B . P L C / P R F / 6
C . H u h H 7
0
0.5
1
1.5
2
2.5
Col I Co lI Col IV FN LN TN VN Neg
OD560nm
control dasatinib
* * * * * *
* *
* *
* *
* *
0
0.5
1
1.5
2
Col I Co lI Col IV FN LN TN VN Neg
OD560nm
control dasatinib
* * * *
* *
* *
* *
* *
* *
0
0.5
1
1.5
2
2.5
3
Col I Co lI Col IV FN LN TN VN Neg
OD560nm
control dasatinib
* *
* * * * * *
* * * *
Figure 9