This document describes the design and testing of a novel multi-epitope peptide vaccine against hepatocellular carcinoma (HCC). Bioinformatics tools were used to design a vaccine construct containing epitopes that could provoke both humoral and cellular immune responses. The vaccine protein was expressed in E. coli and its expression was confirmed using SDS-PAGE and Western blot analysis. The results showed that E. coli is an acceptable system for producing the recombinant multi-epitope peptide vaccine against HCC.
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https://ihc-prs.com/contact/
Immunohistochemistry is a widely available technique that is less challenging and can provide clinically meaningful results quickly and cost-efficiently in comparison with other techniques. In addition, immunohistochemistry allows for the evaluation of cellular localization of proteins in the context of tumor structure.
Oncolytic Virus Therapy Development - Creative BiolabsCreative-Biolabs
Oncolytic virotherapy is cancer treatment using a native or reprogrammed virus that has the potential to targeting and killing cancerous cell. Taking advantage of the OncoVirapy™ platform, Creative Biolabs provides customized, standardized, and reliable and high-quality oncolytic virus therapy development services for clients globally.
Proteogenomic analysis of human colon cancer reveals new therapeutic opportun...Gul Muneer
We performed the first proteogenomic study on a prospectively collected colon cancer cohort. Comparative proteomic and phosphoproteomic analysis of paired tumor and normal adjacent tissues produced a catalog of colon cancer-associated proteins and phosphosites, including known and putative new biomarkers, drug targets, and cancer/testis antigens. Proteogenomic integration not only prioritized genomically inferred targets, such as copy-number drivers and mutation-derived neoantigens, but also yielded novel findings. Phosphoproteomics data associated Rb phosphorylation with increased proliferation and decreased apoptosis in colon cancer, which explains why this classical tumor suppressor is amplified in colon tumors and suggests a rationale for targeting Rb phosphorylation in colon cancer. Proteomics identified an association between decreased CD8 T cell infiltration and increased glycolysis in microsatellite instability-high (MSI-H) tumors, suggesting glycolysis as a potential target to overcome the resistance of MSI-H tumors to immune checkpoint blockade. Proteogenomics presents new avenues for biological discoveries and therapeutic development.
https://ihc-prs.com/contact/
Immunohistochemistry is a widely available technique that is less challenging and can provide clinically meaningful results quickly and cost-efficiently in comparison with other techniques. In addition, immunohistochemistry allows for the evaluation of cellular localization of proteins in the context of tumor structure.
A normal cell can be transformed into a cancerous cell. Discuss the therapeutic strategies that are employed to target the cellular transformation process for cancer prevention and treatment.
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PEGS Korea 2015 the essential protein engineering summitNicole Proulx
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PEGS Korea 2015 the essential protein engineering summitNicole Proulx
PEGS is Cambridge Healthtech institute (CHI)’s flagship biologics meeting, and is widely considered the industry’s leading event on protein and antibody engineering. Its successful accolades include an annual attendance of over 1800 participants at the PEGS Summit in Boston; a record attendance of over 500 attendees at PEGS Europe this year; a successful launch of PEGS China in 2014, and now, the announcement of the first PEGS Korea to be launched in September 2015.
The 3-day Inaugural PEGS Korea will bring together an international faculty consisting of scientists, engineers and executives from all over the world to share their expertise and experiences in protein and antibody engineering, particularly in developing next-generation therapeutics including ADCs, bispecifics, and immunomodulating antibodies.
A normal cell can be transformed into a cancerous cell. Discuss the therapeutic strategies that are employed to target the cellular transformation process for cancer prevention and treatment.
Low expression of N-myc downstream-regulated gene 2 in oesophageal squamous c...Enrique Moreno Gonzalez
It is currently unclear whether a correlation exists between N-myc downstream-regulated gene 2 (NDRG2) expression and oesophageal squamous cell carcinoma (ESCC). The aim of this study was to examine the underlying clinical significance of NDRG2 expression in ESCC patients and to investigate the effects of NDRG2 up-regulation on ESCC cell growth in vitro and in vivo.
How many patients does case series should have In comparison to case reports.pdfpubrica101
Pubrica’s team of researchers and writers create scientific and medical research articles, which may be important resources for authors and practitioners. Pubrica medical writers assist you in creating and revising the introduction by alerting the reader to gaps in the chosen study subject. Our professionals understand the order in which the hypothesis topic is followed by the broad subject, the issue, and the backdrop.
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2. INTRODUCTION
Hepatocellular carcinoma (HCC) is the seventh most prevalent liver
cancer in the world and the fourth leading cause of cancer mortality
worldwide.
The carcinoma consists of epithelial cells, which are the cells that
line the inner and outer parts of the body.
Treatments against this type of cancer are scarce and it depends on
the stage of the cancer. Patients can be treated with surgery or
chemotherapy with sorafenib.
3. INTRODUCTION
Researches have used adoptive immunotherapy as indirect
immunological approaches including vaccines.
Vaccines are an effective strategy against tumor cells and are
generally divided into three types, including pulsed dendritic cells
(DCs), peptide-based vaccines, and DNA-based vaccines.
Multi-epitope peptide vaccines are used against pathogenic bacteria,
viruses, and tumor cells.
5. Designed Vaccine Construct
Expression of the Vaccine Protein
Materials and Methods
It was used bioinformatical servers (IEDB, ProPred-I
PAComplex and PAComplex ) for the design of a
novel multi-epitope peptide vaccine against HCC.
The media culture of E. coli was at 37° and 1 mL was diluted in
ampicillin. Then it was shaken induced via two different
concentrations of (IPTG). This process was to transform the cells
via centrifugation and the obtained pellets
6. Western Blot Test
SDS-PAGE Análisis
Materials and Methods
It was used to prove the expresión of the vaccine. This is a
technique used to identify a specific protein. The method
involves the use of gel electrophoresis to separate the proteins
in the sample.
It is used to separate proteins according to their
electrophoretic mobility. It is widely used to quantify,
compare and characterize proteins. Constitutes the
input technique for the performance of Western
Blotting
7. Results
The SDS-PAGE technique allowed to analyses of the
multi-epitope peptide
expression of the vaccine.
The result of SDS-PAGE analysis of the
multi-epitope peptide vaccine purification.
9. Author What the autor says Agree or
disagree
Sawada Y, Yoshikawa T,
Ofuji K, Yoshimura
M, Tsuchiya N, Takahashi M
The linear and conformational B-cell
epitopes and interferon-gamma-inducing
epitopes were recognized in the vaccine
construct, because provoking the humoral
and cellular immune responses is
essential in multiepitope peptide
vaccines.3
Agree
Li J, Xing Y, Zhou Z, Yao W,
Cao R, Li T
HCC is a cancer with a high mortality rate.
This malignancy is not usually diagnosed
in the primary stages, because it is known
as a heterogeneous disorder that includes
several etiological agents; therefore, it is
diagnosed in the advanced stages, when
it is usually late for treatment.
Agree
Gravel P, Golaz O. To prove the expression and purification
oft he recombinant vaccine protein, the
Western blot method was employed.
Agree
Discussions
10. Conclusions
E. coli is an acceptable organism to
represent recombinant proteins. This prokaryotic cell
allowed acceptable implementation techniques for
producing multi-epitope
peptide vaccine against HCC
Computer tools were of great help in creating a
novel multi-epitope peptide vaccine against HCC
Editor's Notes
Treatments against this type of cancer are scarce and it depends on the stage of the cancer. Patients can be treated with surgery (Primary Phase) or chemotherapy with sorafenib. But only 10% of patients survive more than three years.
In recent years, researchers have used three main approaches to stimulate the immune response against HCC, including adoptive immunotherapy as indirect immunological approaches including vaccines.
Vaccines, which belong to the indirect immunological strategies, are an effective strategy against tumor cells and are generally divided into three types, including pulsed dendritic cells (DCs), peptide-based vaccines, and DNA-based vaccines.
Research has shown Multi-epitope peptide vaccines are used against pathogenic bacteria, viruses, and tumor cells. This consist of Cytotoxic T cell Lymphocytes (CTL) and Helper T cell Lymphocytes (HTL) epitopes, and provoke humoral and adaptive immune responses, these are considered as a beneficial treatment for tumor immunotherapy
It was used bioinformatical servers (IEDB, ProPred-I PAComplex and PAComplex ) for the design of a novel multi-epitope peptide vaccine against HCC. It includes building peptides as MHC class-I peptides.
The media culture of E. coli was at 37° overnight. After that, 1 mL was diluted in ampicillin. Then it was shaken until an optical Density. The culture was induced via two different concentrations of Isopropyl β-D-1-thiogalactopyranoside (IPTG). The transformed cells were harvested via centrifugation and the obtained pellets were stored at -20.
It is used to separate proteins according to their electrophoretic mobility. It is widely used to quantify, compare and characterize proteins. Constitutes the input technique for the performance of Western Blotting
It was used to prove the expresión of the vaccine. This is a technique used to identify a specific protein. The method involves the use of gel electrophoresis to separate the proteins in the sample. Then the proteins are transferred to a membrane which exposes an antibody against the protein. Functional binding is detected using a radioactive or chemical tracer.
The SDS-PAGE technique allowed to analyses of the multi-epitope peptide expression of the vaccine. The line 2 shows the expressed protein before expression induction, and lines 3-6 show the protein expression after Expression. The black circle represents the optimal protein expression.
The result of SDS-PAGE analysis of the multi-epitope peptide vaccine purification. Line 1 shows transformed E. coli after expression. lines 2-3 show the unpurified peptide, and line 4 shows the purified peptide vaccine.
Line 1 shows the purified protein using the Western blot technique.