This document discusses tumor markers and their use in cancer screening and care. It defines tumor markers as substances produced by tumor cells or other cells in response to tumors that can be detected in blood, fluids, or tissues. The document describes how tumor markers are used to aid in diagnosis, identify cancer type and stage, monitor treatment effectiveness, and screen high-risk populations. It also discusses different types of tumor markers and provides guidance on choosing markers for specific cancer types.
Tumour Markers are substances present in the tumour, produced by the tumour or by the host as a response to the presence of the tumour, providing information about biological characteristics of the tumour. these tumour markers may specific for the tissue but often get elevated in neoplastic as well non-neoplastic lesions, further Various analytical platforms available for serum tumour markers lack standardisation. These factors add to interpretative challenges in serum tumour markers
Tumor markers can play roles in early detection, diagnosis, prognosis, monitoring treatment response, and detecting recurrence of certain cancers. This document discusses various tumor markers including their reference ranges, associated cancers, clinical applications, and methods of detection. Key points covered include the roles of AFP for liver cancer screening, CEA and CA19-9 for colorectal cancer monitoring, PSA for prostate cancer screening and follow up, and CA125 for ovarian cancer treatment assessment and recurrence detection. The document also provides recommendations for optimal use of tumor marker tests.
Tumor markers are substances produced by cancer cells or other cells in response to cancer that can be detected in bodily fluids or tissues. The ideal tumor marker would be highly sensitive and specific to a cancer, produced early in cancer progression, and correlated with tumor burden. Common tumor markers include AFP for liver and germ cell cancers, CEA for gastrointestinal cancers, PSA for prostate cancer, CA125 for ovarian cancer, and calcitonin for thyroid cancer. Tumor markers have applications in cancer screening, diagnosis, staging, determining prognosis, monitoring treatment response, and detecting recurrence.
Tumor markers are biological substances released by tumor cells or the body in response to tumors. They can be detected in bodily fluids and indicate the presence or progression of cancer. While no single tumor marker is perfect, they can be useful for screening, diagnosis, staging, prognosis, monitoring treatment response, and detecting recurrence. Common tumor markers include CEA, AFP, CA19-9, PSA, CA125, and hormone receptors. A variety of detection methods exist. While beneficial, tumor markers also have limitations like elevated levels in benign conditions and lack of presence in some cancer types. Continual research aims to improve tumor marker tests and discover new markers.
Tumor markers (also known as biomarkers) are substances found at higher than normal levels in the blood, urine, or body tissue of some people with cancer. Although cancer cells often produce tumor markers, other healthy cells in the body produce them as well.
Tumor Biomarkers For Screening, Progression and Prognosis Vivek Misra
Tumor markers are substances that can be found in the body (usually in the blood or urine) when cancer is present. Along with other tests, tumor markers can be used to help show if cancer is present, to determine the type of cancer, and in some cases to help show if treatment is working. Some of the more common tumor markers are discussed here.
Tumor markers are biomarkers found in blood, urine, or tissues that can indicate the presence of cancer when elevated. They can be produced directly by tumors or other cells in response to tumors. While tumor marker assays help with cancer staging and treatment, they are usually not definitive diagnostic tests and biopsy is required for diagnosis. Tumor markers include proteins, peptides, and carbohydrates and can be used for cancer screening, monitoring recurrence, diagnosis, staging, prognosis, evaluating treatment effectiveness, and as companion diagnostics. Commonly used tumor markers include alpha fetoprotein, CA15-3, CA27-29, CA19-9, and CA-125.
This document discusses tumor markers, which are substances that can indicate the presence of cancer. It defines tumor markers as products of cancer cells or the body's response to cancer that are usually found in blood or urine. However, tumor markers alone cannot diagnose or rule out cancer. The document then classifies different types of tumor markers such as antigens, enzymes, hormones, oncofetal proteins, and tumor-associated antigens. It explains how tumor markers can be used for cancer screening, diagnosis, determining prognosis and treatment effectiveness, and detecting cancer recurrence. Key tumor markers are discussed for different cancer types.
Tumour Markers are substances present in the tumour, produced by the tumour or by the host as a response to the presence of the tumour, providing information about biological characteristics of the tumour. these tumour markers may specific for the tissue but often get elevated in neoplastic as well non-neoplastic lesions, further Various analytical platforms available for serum tumour markers lack standardisation. These factors add to interpretative challenges in serum tumour markers
Tumor markers can play roles in early detection, diagnosis, prognosis, monitoring treatment response, and detecting recurrence of certain cancers. This document discusses various tumor markers including their reference ranges, associated cancers, clinical applications, and methods of detection. Key points covered include the roles of AFP for liver cancer screening, CEA and CA19-9 for colorectal cancer monitoring, PSA for prostate cancer screening and follow up, and CA125 for ovarian cancer treatment assessment and recurrence detection. The document also provides recommendations for optimal use of tumor marker tests.
Tumor markers are substances produced by cancer cells or other cells in response to cancer that can be detected in bodily fluids or tissues. The ideal tumor marker would be highly sensitive and specific to a cancer, produced early in cancer progression, and correlated with tumor burden. Common tumor markers include AFP for liver and germ cell cancers, CEA for gastrointestinal cancers, PSA for prostate cancer, CA125 for ovarian cancer, and calcitonin for thyroid cancer. Tumor markers have applications in cancer screening, diagnosis, staging, determining prognosis, monitoring treatment response, and detecting recurrence.
Tumor markers are biological substances released by tumor cells or the body in response to tumors. They can be detected in bodily fluids and indicate the presence or progression of cancer. While no single tumor marker is perfect, they can be useful for screening, diagnosis, staging, prognosis, monitoring treatment response, and detecting recurrence. Common tumor markers include CEA, AFP, CA19-9, PSA, CA125, and hormone receptors. A variety of detection methods exist. While beneficial, tumor markers also have limitations like elevated levels in benign conditions and lack of presence in some cancer types. Continual research aims to improve tumor marker tests and discover new markers.
Tumor markers (also known as biomarkers) are substances found at higher than normal levels in the blood, urine, or body tissue of some people with cancer. Although cancer cells often produce tumor markers, other healthy cells in the body produce them as well.
Tumor Biomarkers For Screening, Progression and Prognosis Vivek Misra
Tumor markers are substances that can be found in the body (usually in the blood or urine) when cancer is present. Along with other tests, tumor markers can be used to help show if cancer is present, to determine the type of cancer, and in some cases to help show if treatment is working. Some of the more common tumor markers are discussed here.
Tumor markers are biomarkers found in blood, urine, or tissues that can indicate the presence of cancer when elevated. They can be produced directly by tumors or other cells in response to tumors. While tumor marker assays help with cancer staging and treatment, they are usually not definitive diagnostic tests and biopsy is required for diagnosis. Tumor markers include proteins, peptides, and carbohydrates and can be used for cancer screening, monitoring recurrence, diagnosis, staging, prognosis, evaluating treatment effectiveness, and as companion diagnostics. Commonly used tumor markers include alpha fetoprotein, CA15-3, CA27-29, CA19-9, and CA-125.
This document discusses tumor markers, which are substances that can indicate the presence of cancer. It defines tumor markers as products of cancer cells or the body's response to cancer that are usually found in blood or urine. However, tumor markers alone cannot diagnose or rule out cancer. The document then classifies different types of tumor markers such as antigens, enzymes, hormones, oncofetal proteins, and tumor-associated antigens. It explains how tumor markers can be used for cancer screening, diagnosis, determining prognosis and treatment effectiveness, and detecting cancer recurrence. Key tumor markers are discussed for different cancer types.
Tumor markers are proteins or mutated proteins that can indicate the presence of cancer. They are useful for screening, diagnosis, monitoring treatment and detecting recurrence, though none are sufficiently sensitive and specific for screening alone. Tumor markers associated with cell proliferation, differentiation, metastasis and other tumor events can provide information about cancer. While not diagnostic, they are helpful for treatment monitoring given their limitations. Proper use requires understanding their sensitivity, specificity and potential causes of false positives.
Biomarkers can be used for screening, diagnosis, prognosis, and predicting response to treatment for cancer. In bladder cancer, screening biomarkers could identify high-risk groups but population screening may lead to many false positives. Diagnostic biomarkers are needed because hematuria is non-specific, and cystoscopy is expensive. Prognostic biomarkers help determine disease course as response can vary between patients with similar pathology. Predictive biomarkers identify subgroups likely to benefit from specific therapies.
Biomarkers have a diversified role in diagnosis, prognostication and risk stratification. This presentation aims to compile the basic information and new literature on various biomarkers pertaining to cancer care.
This document discusses serum tumor markers, which are molecules that can be detected in blood, body fluids, or tissue that are produced by or in response to cancer cells. It describes several commonly used tumor markers, including their history, clinical uses, and interpretations. The key tumor markers discussed are alpha-fetoprotein (AFP) for hepatocellular carcinoma and germ cell tumors, carcinoembryonic antigen (CEA) for colorectal cancer, CA-125 for ovarian cancer, human chorionic gonadotropin (hCG) for gestational trophoblastic tumors, prostate-specific antigen (PSA) for prostate cancer, CA 19-9 for pancreatic cancer, and CA 15-3
Tumor markers are substances produced by tumors or the body's response to tumors that can help detect and monitor cancer. Alpha-fetoprotein (AFP) is elevated in hepatocellular carcinoma and germ cell tumors. It is useful for diagnosis, staging, prognosis, and monitoring treatment response in HCC and germ cell tumors. Carcinoembryonic antigen (CEA) is elevated in various cancers including colorectal cancer. CEA levels correlate with tumor stage and burden and can help monitor treatment response and detect recurrence, though it lacks sensitivity and specificity for screening and diagnosis.
Tumor markers are substances produced by tumor cells or the body's response to tumors that can be detected and measured in bodily fluids or tissues. They can help diagnose certain cancers, distinguish between benign and malignant tumors, monitor treatment response and detect recurrence. However, no single tumor marker is perfect as tumor marker levels can also be elevated in some non-cancerous conditions.
This document discusses tumor markers, which are biological substances that can indicate the presence of cancer. It describes several potential uses of tumor markers, including screening, diagnosis, prognosis, and monitoring treatment. Several specific tumor markers are mentioned, such as CA 15-3, CA 27-29, HER2, and hormone receptors. The document notes that an ideal tumor marker would be highly sensitive and specific, correlate with tumor stage and mass, and predict prognosis. However, no single marker is perfect, and research is ongoing to discover new markers and improved methods of detection such as genomics and proteomics.
What is biomarker?
What is the purpose of biomarker
Processes of biomarker development?
Types of Biomarkers
What is biomarker testing for cancer treatment?
Uses of Biomarkers in Cancer Medicine
Uses of Biomarkers in Cancer Drug Discovery
The document summarizes the role of innate and adaptive immune cells in the tumor microenvironment and their effect on tumor growth. It discusses how the tumor microenvironment can influence immune cells and how immune cells can affect tumor progression. Key cells discussed include macrophages, neutrophils, NK cells, T cells, B cells, dendritic cells, and regulatory T cells. It covers topics like hypoxia, inflammation, immune evasion mechanisms used by tumors, and the pro-tumoral phenotypes that immune cells can adopt in the microenvironment.
Tumour markers are substances related to the presence or progress of cancer. Common tumour markers include hormones, enzymes, and tumour antigens. They can be used to monitor treatment response, assess follow-up, aid in diagnosis using blood or biopsy samples, and provide prognostic information. Specific high-risk populations can also be screened using tumour markers like calcitonin for thyroid cancer. Important individual tumour markers include alkaline phosphatase, lactate dehydrogenase, prostate-specific antigen, human chorionic gonadotropin, alpha-fetoprotein, and carcinoembryonic antigen.
The document discusses the Warburg effect, where cancer cells preferentially use glycolysis over oxidative phosphorylation to generate energy, even in the presence of oxygen. This allows cancer cells to rapidly proliferate by generating ATP and biomass through glycolysis. The effect occurs because cancer cells overexpress hypoxia-inducible factor 1, increasing glycolytic enzymes and decreasing mitochondrial function. While the exact cause is still unknown, the Warburg effect provides cancer cells a growth advantage and is exploited in PET scanning and as a target for potential anticancer drugs.
Molecular profiling of breast cancer can classify tumor types, identify appropriate therapeutic targets, determine prognosis, and predict treatment response. Techniques include immunohistochemistry, fluorescence in situ hybridization, reverse transcription PCR, microarrays, and next generation sequencing to analyze protein expression, gene copy number, mutations, and gene expression levels. Breast cancers are classified into intrinsic subtypes including luminal A/B, HER2-enriched, basal-like, and claudin-low based on distinct gene expression patterns that predict clinical behavior and response to therapy.
Tumour markers can play a crucial role in detecting cancer and assessing response to therapy. They are substances produced either by tumour cells or by the body in response to cancer. Oncoproteins are proteins encoded by oncogenes which normally maintain a fine balance between cell proliferation and differentiation but become permanently activated in cancer, stimulating cell growth. Elevated levels of various oncoproteins and other tumour markers can be detected in blood and other body fluids, serving as biomarkers for early cancer detection and prediction of prognosis. Common tumour markers discussed include AFP, CEA, CA19-9, CA15-3, CA125, and proteins associated with growth factors, receptors, and cellular signalling pathways.
This document discusses the use of immunohistochemistry in breast pathology. It covers several topics:
1. Analyzing prognostic markers like hormone receptors in breast cancer and their predictive value.
2. Using myoepithelial cell markers to help solve diagnostic dilemmas and distinguish lesions.
3. Identifying tumor subtypes and assessing diagnoses using markers like luminal vs basal.
4. Evaluating cell populations in proliferative breast lesions and assessing neoplasia vs hyperplasia.
Introduction to cancer biology nerdy scientiststazib rahaman
This document discusses cancer initiation, promotion, and progression. It defines initiation as the creation of abnormal DNA from carcinogens. Promoters then stimulate replication of these neoplastic cells and tumor development. Enhancers increase the likelihood that nearby genes will be transcribed. Gene amplification and point mutations can further cancer progression. The document also summarizes a study finding COVID-19 infection is associated with severe outcomes in cancer patients, especially those undergoing immunosuppressive therapy, recommending screening and decreased immunosuppressive treatment during the pandemic.
A comprehensive presentation on cancer biochemistry including biochemical changes,carcinogens,mechanism of chemical carcinogenesis ,oncogenes & activation,monoclonal antibodies for cancer therapy,diet ,prevention &tumor markers
Tumor markers are substances produced by tumors or the host body in response to tumors. They can be used to detect cancers, determine cancer prognosis, and monitor cancer treatment effectiveness. Some key tumor markers discussed in the document include:
- AFP which is used to detect hepatocellular carcinoma and testicular cancer.
- CEA which is used to detect colorectal cancer recurrence. Rising CEA levels may indicate cancer recurrence while stable levels indicate remission.
- CA125 which is used to detect ovarian and endometrial cancers.
- PSA which is used to screen, stage, and monitor prostate cancer recurrence and treatment.
- HCG which is used to detect germ
Tumour markers are substances that are produced by tumour cells or the body's response to tumours that can be detected and measured in blood, urine, or body tissues. They can be used for screening, diagnosis, staging, detecting recurrence, and monitoring treatment response. However, tumour markers have limitations as they are not always tumour-specific and levels can be elevated in benign conditions. The main uses of common tumour markers are monitoring disease in patients with known cancers like CEA for colorectal cancer, PSA for prostate cancer, and AFP and HCG for germ cell tumours.
This document defines key terms related to cancer biomarkers. It describes cancer as abnormal cell growth and discusses cancer staging and tumor markers. Biomarkers are defined as indicators of biological processes that can be tested from bodily fluids or tissues. Common tumor markers are described, including alpha-fetoprotein, cancer antigen 125, carcinoembryonic antigen, human chorionic gonadotropin, and prostate-specific antigen. The roles of these markers in cancer screening, diagnosis, staging, prognosis, and monitoring treatment are summarized.
Tumor markers are substances produced by tumor cells or the body's response to tumors that can be detected in blood, urine, or tissue. They can be used to screen for cancers, help diagnose cancer when the primary site is unknown, stage cancers, determine prognosis, and monitor treatment effectiveness. The most widely accepted tumor markers are prostate-specific antigen for prostate cancer screening and alpha-fetoprotein plus ultrasound for screening for hepatocellular carcinoma in endemic areas. Elevated levels of markers like gastrin and insulin are diagnostic for certain neuroendocrine tumors.
Tumor markers are proteins or mutated proteins that can indicate the presence of cancer. They are useful for screening, diagnosis, monitoring treatment and detecting recurrence, though none are sufficiently sensitive and specific for screening alone. Tumor markers associated with cell proliferation, differentiation, metastasis and other tumor events can provide information about cancer. While not diagnostic, they are helpful for treatment monitoring given their limitations. Proper use requires understanding their sensitivity, specificity and potential causes of false positives.
Biomarkers can be used for screening, diagnosis, prognosis, and predicting response to treatment for cancer. In bladder cancer, screening biomarkers could identify high-risk groups but population screening may lead to many false positives. Diagnostic biomarkers are needed because hematuria is non-specific, and cystoscopy is expensive. Prognostic biomarkers help determine disease course as response can vary between patients with similar pathology. Predictive biomarkers identify subgroups likely to benefit from specific therapies.
Biomarkers have a diversified role in diagnosis, prognostication and risk stratification. This presentation aims to compile the basic information and new literature on various biomarkers pertaining to cancer care.
This document discusses serum tumor markers, which are molecules that can be detected in blood, body fluids, or tissue that are produced by or in response to cancer cells. It describes several commonly used tumor markers, including their history, clinical uses, and interpretations. The key tumor markers discussed are alpha-fetoprotein (AFP) for hepatocellular carcinoma and germ cell tumors, carcinoembryonic antigen (CEA) for colorectal cancer, CA-125 for ovarian cancer, human chorionic gonadotropin (hCG) for gestational trophoblastic tumors, prostate-specific antigen (PSA) for prostate cancer, CA 19-9 for pancreatic cancer, and CA 15-3
Tumor markers are substances produced by tumors or the body's response to tumors that can help detect and monitor cancer. Alpha-fetoprotein (AFP) is elevated in hepatocellular carcinoma and germ cell tumors. It is useful for diagnosis, staging, prognosis, and monitoring treatment response in HCC and germ cell tumors. Carcinoembryonic antigen (CEA) is elevated in various cancers including colorectal cancer. CEA levels correlate with tumor stage and burden and can help monitor treatment response and detect recurrence, though it lacks sensitivity and specificity for screening and diagnosis.
Tumor markers are substances produced by tumor cells or the body's response to tumors that can be detected and measured in bodily fluids or tissues. They can help diagnose certain cancers, distinguish between benign and malignant tumors, monitor treatment response and detect recurrence. However, no single tumor marker is perfect as tumor marker levels can also be elevated in some non-cancerous conditions.
This document discusses tumor markers, which are biological substances that can indicate the presence of cancer. It describes several potential uses of tumor markers, including screening, diagnosis, prognosis, and monitoring treatment. Several specific tumor markers are mentioned, such as CA 15-3, CA 27-29, HER2, and hormone receptors. The document notes that an ideal tumor marker would be highly sensitive and specific, correlate with tumor stage and mass, and predict prognosis. However, no single marker is perfect, and research is ongoing to discover new markers and improved methods of detection such as genomics and proteomics.
What is biomarker?
What is the purpose of biomarker
Processes of biomarker development?
Types of Biomarkers
What is biomarker testing for cancer treatment?
Uses of Biomarkers in Cancer Medicine
Uses of Biomarkers in Cancer Drug Discovery
The document summarizes the role of innate and adaptive immune cells in the tumor microenvironment and their effect on tumor growth. It discusses how the tumor microenvironment can influence immune cells and how immune cells can affect tumor progression. Key cells discussed include macrophages, neutrophils, NK cells, T cells, B cells, dendritic cells, and regulatory T cells. It covers topics like hypoxia, inflammation, immune evasion mechanisms used by tumors, and the pro-tumoral phenotypes that immune cells can adopt in the microenvironment.
Tumour markers are substances related to the presence or progress of cancer. Common tumour markers include hormones, enzymes, and tumour antigens. They can be used to monitor treatment response, assess follow-up, aid in diagnosis using blood or biopsy samples, and provide prognostic information. Specific high-risk populations can also be screened using tumour markers like calcitonin for thyroid cancer. Important individual tumour markers include alkaline phosphatase, lactate dehydrogenase, prostate-specific antigen, human chorionic gonadotropin, alpha-fetoprotein, and carcinoembryonic antigen.
The document discusses the Warburg effect, where cancer cells preferentially use glycolysis over oxidative phosphorylation to generate energy, even in the presence of oxygen. This allows cancer cells to rapidly proliferate by generating ATP and biomass through glycolysis. The effect occurs because cancer cells overexpress hypoxia-inducible factor 1, increasing glycolytic enzymes and decreasing mitochondrial function. While the exact cause is still unknown, the Warburg effect provides cancer cells a growth advantage and is exploited in PET scanning and as a target for potential anticancer drugs.
Molecular profiling of breast cancer can classify tumor types, identify appropriate therapeutic targets, determine prognosis, and predict treatment response. Techniques include immunohistochemistry, fluorescence in situ hybridization, reverse transcription PCR, microarrays, and next generation sequencing to analyze protein expression, gene copy number, mutations, and gene expression levels. Breast cancers are classified into intrinsic subtypes including luminal A/B, HER2-enriched, basal-like, and claudin-low based on distinct gene expression patterns that predict clinical behavior and response to therapy.
Tumour markers can play a crucial role in detecting cancer and assessing response to therapy. They are substances produced either by tumour cells or by the body in response to cancer. Oncoproteins are proteins encoded by oncogenes which normally maintain a fine balance between cell proliferation and differentiation but become permanently activated in cancer, stimulating cell growth. Elevated levels of various oncoproteins and other tumour markers can be detected in blood and other body fluids, serving as biomarkers for early cancer detection and prediction of prognosis. Common tumour markers discussed include AFP, CEA, CA19-9, CA15-3, CA125, and proteins associated with growth factors, receptors, and cellular signalling pathways.
This document discusses the use of immunohistochemistry in breast pathology. It covers several topics:
1. Analyzing prognostic markers like hormone receptors in breast cancer and their predictive value.
2. Using myoepithelial cell markers to help solve diagnostic dilemmas and distinguish lesions.
3. Identifying tumor subtypes and assessing diagnoses using markers like luminal vs basal.
4. Evaluating cell populations in proliferative breast lesions and assessing neoplasia vs hyperplasia.
Introduction to cancer biology nerdy scientiststazib rahaman
This document discusses cancer initiation, promotion, and progression. It defines initiation as the creation of abnormal DNA from carcinogens. Promoters then stimulate replication of these neoplastic cells and tumor development. Enhancers increase the likelihood that nearby genes will be transcribed. Gene amplification and point mutations can further cancer progression. The document also summarizes a study finding COVID-19 infection is associated with severe outcomes in cancer patients, especially those undergoing immunosuppressive therapy, recommending screening and decreased immunosuppressive treatment during the pandemic.
A comprehensive presentation on cancer biochemistry including biochemical changes,carcinogens,mechanism of chemical carcinogenesis ,oncogenes & activation,monoclonal antibodies for cancer therapy,diet ,prevention &tumor markers
Tumor markers are substances produced by tumors or the host body in response to tumors. They can be used to detect cancers, determine cancer prognosis, and monitor cancer treatment effectiveness. Some key tumor markers discussed in the document include:
- AFP which is used to detect hepatocellular carcinoma and testicular cancer.
- CEA which is used to detect colorectal cancer recurrence. Rising CEA levels may indicate cancer recurrence while stable levels indicate remission.
- CA125 which is used to detect ovarian and endometrial cancers.
- PSA which is used to screen, stage, and monitor prostate cancer recurrence and treatment.
- HCG which is used to detect germ
Tumour markers are substances that are produced by tumour cells or the body's response to tumours that can be detected and measured in blood, urine, or body tissues. They can be used for screening, diagnosis, staging, detecting recurrence, and monitoring treatment response. However, tumour markers have limitations as they are not always tumour-specific and levels can be elevated in benign conditions. The main uses of common tumour markers are monitoring disease in patients with known cancers like CEA for colorectal cancer, PSA for prostate cancer, and AFP and HCG for germ cell tumours.
This document defines key terms related to cancer biomarkers. It describes cancer as abnormal cell growth and discusses cancer staging and tumor markers. Biomarkers are defined as indicators of biological processes that can be tested from bodily fluids or tissues. Common tumor markers are described, including alpha-fetoprotein, cancer antigen 125, carcinoembryonic antigen, human chorionic gonadotropin, and prostate-specific antigen. The roles of these markers in cancer screening, diagnosis, staging, prognosis, and monitoring treatment are summarized.
Tumor markers are substances produced by tumor cells or the body's response to tumors that can be detected in blood, urine, or tissue. They can be used to screen for cancers, help diagnose cancer when the primary site is unknown, stage cancers, determine prognosis, and monitor treatment effectiveness. The most widely accepted tumor markers are prostate-specific antigen for prostate cancer screening and alpha-fetoprotein plus ultrasound for screening for hepatocellular carcinoma in endemic areas. Elevated levels of markers like gastrin and insulin are diagnostic for certain neuroendocrine tumors.
1. cancer care.pdf medical surgical nursing 1akoeljames8543
This document provides an overview of cancer principles and concepts in Kenya. It discusses Kenya's health policy goals to address rising non-communicable diseases like cancer. Cancer arises due to uncontrolled cell growth and can spread through the body. Risk factors include genetics, behaviors, age, and environmental exposures. Diagnosis relies on tissue biopsy. Cancer management involves multidisciplinary teams. Prevention strategies include screening and avoiding risk factors. Genetic testing can assess cancer risk in families with predispositions. The cell cycle is important to understand cancer development.
TUMOUR MARKERS AND CLINICAL EFFECTS OF TUMOR-1.pptxmwalunuym
This document discusses tumour markers and the clinical effects of cancer. It begins by outlining the objectives and providing an introduction to tumour markers. It then describes the clinical uses, ideal characteristics, and classification of tumour markers. The document discusses the local effects of tumours through compression, obstruction, destruction and other means. It also outlines some of the systemic effects of cancer, including cancer cachexia caused by cytokines, inflammation, and metabolic changes. In summary, the document provides an overview of tumour markers and how cancer can affect the body both locally and systemically.
Here are some additional common side effects of chemotherapy:
- Mucositis (inflammation and ulcers in the mouth and gastrointestinal tract)
- Dermatologic effects like rashes, dry skin, nail changes
- Hepatotoxicity and kidney toxicity with some agents
- Cardiotoxicity with agents like doxorubicin
- Secondary cancers and myelodysplasia due to mutagenic effects
- Infertility issues depending on the agents used
It's important for nurses to thoroughly assess for and manage side effects during chemotherapy treatment.
This document defines various tumor markers and their clinical applications. It discusses commonly ordered tumor markers such as alpha-fetoprotein, cancer antigen 125, carcinoembryonic antigen, human chorionic gonadotropin, and prostate-specific antigen. These markers can be used for cancer diagnosis, prognosis, and monitoring treatment effectiveness. However, tumor marker levels are not specific to cancer and can be elevated in certain non-cancerous conditions. Enzymes were among the first tumor markers identified but provide only nonspecific indications of malignancy.
This document provides an overview of molecular diagnostic methods for liver cancer. It discusses detecting cancer-related genes, genes of related viruses like HBV and HCV, and markers of liver cancer. Common markers are alpha-fetoprotein, GGT, and CA125. Detection methods include PCR, gene chips, radioimmunoassay, ELISA, and chemiluminescent, fluorescent, and electrochemiluminescent immunoassay systems. The document concludes that combining detection of multiple markers is more effective than single markers and will improve early diagnosis as methods advance.
Tumor markers are substances produced by tumors or the body's response to tumors that can be detected and measured in blood, urine, or body tissues. They can help monitor treatment response, detect recurrence, and provide prognostic information. However, no single tumor marker is perfect, as they may be elevated in benign conditions and not all cancer patients exhibit increased levels. The most useful tumor markers are those that correlate with tumor burden and stage and are cancer-specific.
The document provides an overview of cancer biology, including key terminology, epidemiology, etiology, prevention, screening, diagnosis, staging, treatment, and biomarkers. It defines various types of cancers and neoplasms, describes the cellular and genetic events leading to cancer development, and outlines the general principles and goals of cancer treatment, which may include surgery, chemotherapy, radiation therapy, and palliative care.
Cellular and Molecular Tumor Markers by Prof. Mohamed Labib Salem, PhD (Lux...Prof. Mohamed Labib Salem
This document provides an overview of cellular and molecular tumor markers. It discusses what cancer and tumors are, different types of tumor markers including cellular markers, and applications of tumor markers such as detection, diagnosis and monitoring treatment response. Evaluation criteria for tumor markers like sensitivity and specificity are covered. Common tumor markers used for specific cancer types are listed. Methods for measuring tumor markers like ELISA, PCR, immunohistochemistry and mass spectrometry are described. Limitations of tumor markers are also noted.
Cancer is the second leading cause of death worldwide after cardiovascular disease. In India, an estimated 2.25 million people are living with cancer, with over 11 lakh new cases registered annually. Some key statistics for India include one woman dying of cervical cancer every 8 minutes and two women dying of breast cancer for every one diagnosed. Tumor markers are substances produced by cancerous tissues or the body in response to cancer that can help detect or monitor cancer. Some common tumor markers are CEA, AFP, CA125, and PSA. Tumor markers can be used for screening, diagnosis, staging, prognosis, and monitoring treatment effectiveness and recurrence. Characteristics of ideal tumor markers include cancer specificity, high sensitivity and specificity for detection
In the recent years, knowledge about cancer biomarkers has increased tremendously
providing great opportunities for improving the management of cancer patients by
enhancing the efficiency of detection and efficacy of treatment.
• Recent technological advancement has enabled the examination of many
potential biomarkers and renewed interest in developing new biomarkers.
• Biomarkers of cancer could include a broad range of biochemical entities, such as nucleic
acids, proteins, sugars, lipids, and small metabolites, cytogenetic and cytokinetic
parameters as well as whole tumour cells found in the body
fluid. A COMPREHENSIVE UNDERSTANDING OF THE RELEVANCE
OF EACH BIOMARKER WILL BE VERY IMPORTANT NOT
ONLY FOR DIAGNOSING THE DISEASE RELIABLY, BUT ALSO
HELP IN THE CHOICE OF MULTIPLE THERAPEUTIC
ALTERNATIVES CURRENTLY AVAILABLE THAT IS LIKELY TO
BENEFIT THE PATIENTS.• Measure or evaluate the normal biological process, pathogenic processes, or
pharmacological response to a therapeutic interventions.
• Includes ~ diagnostic test and imaging technology
• “ Cancer is clusters disease involving alterations in status and expression of
multiple genes that confer a survival advantage & diminished proliferative
potential to somatic or germinal cells"
Specific to tumor
• Level change in response to tumor size
• No fluctuations in level
• Low level in healthy individual
• Predict recurrence
• Test should be cost effective
DNA methylation
2. Alteration pattern of histone modification
3. Alterations in chromatin condensation
Breast cancer & biomarkers, their types, novelty of breast cancer biomarkers. Detailed study of her2, p53, BRCA1, BRCA2, DPD, 21-Gene signature, 70-Gene signature, cd106, vcam1, nlr, bFGF, mammaglobin, ER, PR, CEA. Pthological samples for biomarkers test, Ranges of various biomarkers, breast cancer diagnosis, prognosis, occurance, selection of breast caner treatment like targeted therapy.
Cancer biomarkers are measurable indicators of biological states or conditions that can help diagnose, prognosticate, and predict responses to treatment. Biomarkers can include proteins, gene mutations, extra or missing genes, and other molecules secreted by tumors or representing body responses to cancer. Some commonly used cancer biomarkers measure levels of proteins like HER2, PSA, CA125, and carcinoembryonic antigen to diagnose specific cancer types, determine prognosis, monitor therapy effectiveness, and detect recurrence of cancers like breast, prostate, ovarian, and colon cancer. Biomarkers play an important role in developing and applying new cancer therapies.
Cancer is characterized by abnormal cell growth that can invade other tissues and spread to other parts of the body. There are several types of cancer including carcinoma, sarcoma, leukemia, and lymphomas. Cancer is a leading cause of death worldwide, responsible for over 9 million deaths in 2018. Risk factors include tobacco, alcohol, diet, obesity, viruses, and genetic factors. Diagnosis involves physical exams, lab tests, imaging, and biopsies. Treatment options are surgery, radiation, chemotherapy, immunotherapy, hormone therapy, stem cell transplants, and angiogenesis inhibitors. Future prospects for cancer treatment involve more precisely targeting cancers based on their specific genetic changes.
Tumor markers
Many cancers are associated with the abnormal production of some molecules which can be measured in plasma. These molecules are known as tumor markers.
A good tumor maker should have those properties:
1. A tumor marker should be present in or produced by tumor itself.
2. A tumor marker should not be present in healthy tissues.
3. Plasma level of a tumor marker should be at a minimum level in healthy subjects and in benign conditions.
4. A tumor marker should be specific for a tissue, it should have different immunological properties when it is synthesized in other tissues.
5. Plasma level of the tumor marker should be in proportion to the both size of the tumor and the activity of the tumor.
6. Half-life of a tumor should not be very long
7. A tumor marker should be present in plasma at a detectable level, even though tumor size is very small
The document provides information about oncology nursing including objectives, cancer pathophysiology, risk factors, prevention, screening, detection methods, grading and staging of cancer, common cancer types, and nursing interventions. Key points include identifying risk factors from a patient's history, formulating nursing diagnoses, utilizing interventions to maintain health, providing spiritual care, and displaying caring behavior in the delivery of cancer nursing care.
This document discusses epithelial tumor markers. It begins by introducing the topic and defining tumor markers as substances produced by or in response to tumors that can be used to detect or characterize tumors. It then describes the ideal properties of tumor markers and various ways to classify them, including as cell surface markers, intracellular markers, types associated with tumor growth, suppression, angiogenesis, and invasion. Specific epithelial and other markers are outlined. Finally, uses of tumor markers are summarized, including for screening, diagnosis, staging, prognosis, evaluating treatment response, and detecting recurrence. Cytokeratins are highlighted as important epithelial markers.
This document provides an overview of cancer basics for patient navigators. It begins with acknowledgements and lists competencies covered, which include demonstrating familiarity with cancer screening, diagnosis, treatment and survivorship. It then covers learning objectives such as understanding cancer, screening options, basic treatment types, supportive care services and using professional resources. The document provides information on cancer causes, risk factors, prevention, signs and symptoms, detection methods, staging systems, treatment types including surgery, radiation, chemotherapy and targeted therapy. It also discusses palliative care, complementary therapies and important resources for evidence-based cancer information.
Similar to Tumor markers-screening-for-cancer (20)
Recently, the development of molecular biotechnology allows modifications of viral genomes genetically and optimizes the transformation of available viruses with weak pathogenicity. These methods are used to enhance the oncolytic effect and reduce adverse reactions to maximize both efficacy and safety. Indeed, the oncolytic virus can stimulate a pro-inflammatory tumor environment by enhancing antigen recognition and robust immune responses. It overcomes the immune evasiveness and escape of malignant cells to eliminate the tumor cells.
https://www.creative-biolabs.com/oncolytic-virus/definition-of-an-oncolytic-virus.htm
An oncolytic virus is a form of promising therapeutic tool for the treatment of malignant tumors, which uses viruses to selectively infect and kill tumor cells and further to induce or boost specific antitumor immunity. https://www.creative-biolabs.com/oncolytic-virus/definition-of-an-oncolytic-virus.htm
Oncolytic viruses encoding reporter genes utilized for in vivo molecular imaging are useful to locate the distribution of oncolytic viruses in pre-clinical tests. Optical detection methods mainly include green fluorescent protein (GFP), enhanced GFP (eGFP), discosoma red fluorescent protein (DsRed), and bioluminescence imaging (BLI), which utilizes luciferases. Reporter-encoding oncolytic viruses, including vaccinia virus, adenovirus, herpes simplex virus and vesicular stomatitis virus, allow accurate tracking of gene expression, tumor metastases, viral infection as well as assessment of gene therapy.
https://www.creative-biolabs.com/oncolytic-virus/category-reporter-encoding-oncolytic-virus-293.htm
Vaccinia virus can accommodate more than 30 kb of foreign DNA. Foreign genes can be stably integrated into the viral genome, resulting in efficient and long-term gene expression. The deletion of the viral genes of thymidine kinase (TK) and vaccinia growth factors (VGF) results in enhanced tumor-selectively and antitumor activity, and reduced virus virulence. https://www.creative-biolabs.com/oncolytic-virus/category-pre-made-oncolytic-vaccinia-virus-291.htm
Oncolytic viruses are a class of antitumor agents that selectively kill tumor cells without affecting normal cells. Vaccinia virus (VACV) is a large, enveloped virus that is considered as the most potential live biotherapeutic agent because of its strong oncolytic efficacy and potent antigen presentation capability that can combine well with its natural oncolytic activities for cancer immunotherapy. Many types of modified vaccinia virus have been used for in vitro and in vivo studies, as well as clinical trials.https://www.creative-biolabs.com/oncolytic-virus/category-pre-made-oncolytic-vaccinia-virus-291.htm
Partial deletion of the HSV gene results in superior packaging capacity of >30 kb foreign DNA with low toxicity as an expression vector. Multiple modified purified oncolytic herpes simplex virus (oHSV) products can avoid evading the host immune response and reduce toxicity by gene knock-out, such as ICP0, ICP4, ICP22, ICP27 or ICP47.https://www.creative-biolabs.com/oncolytic-virus/category-pre-made-oncolytic-herpes-simplex-virus-290.htm
Oncolytic viruses are using for the treatment of cancer due to the specific antitumor activity in tumor cells. Herpes simplex virus (HSV) is a human neurogenic dsDNA virus that has the characteristic of life-long latent infection of neurons and allows for long-term transgene expression.https://www.creative-biolabs.com/oncolytic-virus/category-pre-made-oncolytic-herpes-simplex-virus-290.htm
Oncolytic viruses have the potential to powerfully and selectively kill cancer cells and have shown impressive efficacy in preclinical and clinical settings. However, their potential can be restricted by inefficient delivery into the complex tumor environment. Thus, the efficient delivery of oncolytic viruses remains a significant challenge in the field of oncology, limiting their therapeutic effect. https://www.creative-biolabs.com/oncolytic-virus/approaches-to-delivery-of-oncolytic-viruses.htm
Numerous viruses are being developed pre-clinically and clinically. An investigation of all registered clinical trials in 2017 demonstrates 78 interventional trials regarding OVs. This ability for near-universal therapeutic impact in cancer makes OVs a popular therapeutic tool. Today, both preclinical and early-stage clinical trials are intensively investigating the approach to improve oncolytic virotherapy.
https://www.creative-biolabs.com/oncolytic-virus/applications-of-oncolytic-viruses-in-cancer-treatment.htm
To fully optimize oncolytic virotherapy and provide meaningful mechanistic insight, it is important to have representative animal models of oncolysis in various tumor types. https://www.creative-biolabs.com/oncolytic-virus/animal-models-for-oncolytic-virus-study.htm
Abciximab (also known as abcixifiban or c7E3 Fab), is the Fab fragment of the chimeric human-murine, monoclonal antibody 7E3. It is composed of murine variable regions and human constant regions.https://www.creativebiolabs.net/abciximab-overview.htm
Abagovomab is a murine monoclonal anti-idiotypic antibody (MW: 165-175 kDa), produced by a mouse hybridoma and generated against OC125, which serves to functionally imitate the human cancer antigen 125 (CA-125). https://www.creativebiolabs.net/abagovomab-overview.htm
Wnt comprises a diverse family of secreted lipid-modified signaling glycoproteins that are 350-400 amino acids in length. Wnt is an acronym in the field of genetics that stands for 'Wingless/Integrated'.https://www.creativebiolabs.net/wnt-signaling-pathway.htm
TNF works through two receptors, TNFR1 and TNFR2. TNFR1 is the major signal receptor of TNF-α. TNFR2, which mediates limited biological responses, binds to TNF-α and TNF-β. TNF signaling transduction through TNFR1 and TNFR2 can induce a variety of cellular responses, which depends on many factors, including the metabolic state of the cell and the adaptor proteins present in the cell.https://www.creativebiolabs.net/tnf-signaling-pathway.htm
Innate immune receptors, also known as pattern recognition receptors (PRRs), have been identified in the serum, on the cell surface, in endosomes, and in the cytoplasm. Toll-like receptors (TLRs) is one of the particularly important groups of PRRs.https://www.creativebiolabs.net/tlr-signal-pathway.htm
Transforming growth factor beta (TGF-β) is a cytokine that participates in both physiological and pathological processes.https://www.creativebiolabs.net/tgf-beta-signaling-pathway.htm
T-cell receptor (TCR) is a heterodimers composed of α and β peptide chains. TCR is mainly responsible for recognizing the antigens presented by major histocompatibility complex (MHC) molecules on the surface of antigen presenting cells (APC).https://www.creativebiolabs.net/tcr-signal-pathway.htm
Ras, which is a low-molecular-weight GDP/GTP-binding guanine triphosphatase, is the prototypical member of the Ras superfamily of proteins. https://www.creativebiolabs.net/ras-signaling-pathway.htm
Peroxisome proliferator-activated receptors (PPARs) are ligand-activated transcription factors, which are responsible for regulating gene expression.https://www.creativebiolabs.net/ppar-signaling-pathway.htm
PI3K-Akt signaling pathway is one of the important signal transduction pathways in cells. It is involved in regulating cell metabolism, growth, proliferation, survival, transcription and protein synthesis by affecting the activation of downstream effector molecules. https://www.creativebiolabs.net/pi3k-akt-signaling-pathway.htm
Osteoporosis - Definition , Evaluation and Management .pdfJim Jacob Roy
Osteoporosis is an increasing cause of morbidity among the elderly.
In this document , a brief outline of osteoporosis is given , including the risk factors of osteoporosis fractures , the indications for testing bone mineral density and the management of osteoporosis
Here is the updated list of Top Best Ayurvedic medicine for Gas and Indigestion and those are Gas-O-Go Syp for Dyspepsia | Lavizyme Syrup for Acidity | Yumzyme Hepatoprotective Capsules etc
Basavarajeeyam is a Sreshta Sangraha grantha (Compiled book ), written by Neelkanta kotturu Basavaraja Virachita. It contains 25 Prakaranas, First 24 Chapters related to Rogas& 25th to Rasadravyas.
ABDOMINAL TRAUMA in pediatrics part one.drhasanrajab
Abdominal trauma in pediatrics refers to injuries or damage to the abdominal organs in children. It can occur due to various causes such as falls, motor vehicle accidents, sports-related injuries, and physical abuse. Children are more vulnerable to abdominal trauma due to their unique anatomical and physiological characteristics. Signs and symptoms include abdominal pain, tenderness, distension, vomiting, and signs of shock. Diagnosis involves physical examination, imaging studies, and laboratory tests. Management depends on the severity and may involve conservative treatment or surgical intervention. Prevention is crucial in reducing the incidence of abdominal trauma in children.
Histololgy of Female Reproductive System.pptxAyeshaZaid1
Dive into an in-depth exploration of the histological structure of female reproductive system with this comprehensive lecture. Presented by Dr. Ayesha Irfan, Assistant Professor of Anatomy, this presentation covers the Gross anatomy and functional histology of the female reproductive organs. Ideal for students, educators, and anyone interested in medical science, this lecture provides clear explanations, detailed diagrams, and valuable insights into female reproductive system. Enhance your knowledge and understanding of this essential aspect of human biology.
1. Antibodies, antigens, etc. for your research and discovery
Increase Your Efficiency and Value
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Tumor Markers
in Cancer Screening
2. ◆ Is it necessary to detect tumor markers?
It is known that tumors are caused by a combination of genetic and environmental
factors. Their cells are characterized by unlimited proliferation. Usually, most tumors
are asymptomatic in the early and middle stages. When patients with clinical symptoms
come to the clinic, the tumor is too large to be removed, or it has entered the advanced
stage, losing the best treatment opportunity. Therefore, early detection, diagnosis, and
treatment of tumors are the key links in clinical cancer prevention and treatment. For
early detection and diagnosis of tumors, a series of more valuable tumor markers have
been used in clinical practice.
◆ What are tumor markers?
◆ How are tumor markers used in cancer care?
◆ Do different cancer types need to be detected by different tumor markers?
◆ Does the rise in tumor markers mean the presence of cancer?
◆ Can tumor markers be used in cancer screening?
◆ How to choose tumor markers?
Catalogue
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Tumor Markers
in Cancer Screening
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3. Tumor markers (TMs) refer to a class of substances that are directly produced by
tumor cells or other cells of the body in response to tumors during its development
and proliferation stages. Tumor markers essentially are proteins, hormones,
enzymes (isozymes), polyamines, and oncogene products, which presents in the
blood, body fluids, cells or tissues of patients. They can quantitatively and
qualitatively reveal the presence of tumors, which provides strong experimental
basis to estimate what the type of tumor is, what stage of the tumor has been
developed to, the therapeutic effect and prognosis.
1. Auxiliary diagnosis and identification of tumors;
2. Screening high-risk populations of tumors;
3. Monitoring tumor recurrence and metastasis;
4. Observing tumor treatment and efficacy.
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◆ What are tumor markers?
◆ How are tumor markers used in cancer care?
Tumor Markers
in Cancer Screening
4. Many tumor-related markers have been found, and nearly 100 kinds of them are of
clinical value. Based on the chemical characteristics, they can be divided into the
following seven categories:
Embryonic antigen
tumor markers
Glycogen tumor
markers
Hormone tumor
markers
Receptor tumor
markers
Protein tumor
markers
Enzyme tumor
markers
Genomics
tumor markers
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◆ Do different cancer types need to be detected by
different tumor markers?
Tumor Markers
in Cancer Screening
5. • Embryonic Antigen Tumor Markers
Many proteins are secreted only during the embryonic
stage, which stop producing after delivery. When a
tumor occurs, these proteins will re-synthesize and be
secreted, thereby being called embryonic antigen-like
tumor marker.
Alpha-fetoprotein (AFP)—liver cancer, spermatogonia.
Embryonic antigen (CEA)—colorectal cancer,
pancreatic cancer, lung cancer, breast cancer.
• Glycogen Tumor Markers
When normal cells are transformed into malignant
cells, the glycoproteins on the cell surface will
mutate to a specific antigen, which can be detected
by monoclonal techniques. These antigenic
substances presenting on the surface of tumor cells
are called carbohydrate antigens (CA).
CA125—ovarian cancer.
CA15-3—breast cancer, ovarian cancer.
CA19-9—pancreatic cancer, liver cancer, and
gastrointestinal cancer.
CA72-4—gastrointestinal cancer, pancreatic cancer,
ovarian cancer.
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Tumor Markers
in Cancer Screening
6. • Hormone Tumor Markers
When a cell with a secretory hormone function is
cancerous, it will secrete abnormal amount of
hormones. Cells that do not produce hormones begin
to produce hormones after canceration.
Calcitonin (CT)—thyroid tumor.
Human Chorionic Gonadotropin (hCG)—embryonal
carcinoma, choriocarcinoma, non-spermatocytic
carcinoma.
• Receptor Tumor Markers
Receptors are components existing on the cell
membrane or in the cells, which are responsible for
recognizing and binding to a biologically active
molecule. It can correctly amplify and transmit the
recognized and received signals to the interior of the
cell, thereby causing biological effects.
Estrogen Receptor (ER) and Progesterone Receptor
(PR)—breast cancer.
Epidermal Growth Factor (EGFR)—colorectal cancer,
non-small cell lung cancer, head and neck cancer,
breast cancer.
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Tumor Markers
in Cancer Screening
7. 2-2-microglobulin (β2-MG)—multiple myeloma, lymphoma,
leukemia.
Ferritin (SF)—liver cancer, lung cancer, leukemia, breast cancer.
Thyroglobulin-thyroid cancer.
Cytokeratin 19 fragment (Cyfra 21-1)—lung cancer, bladder
cancer, prostate cancer, ovarian cancer, colorectal cancer,
pancreatic cancer.
Tissue polypeptide antigen (TPA)—bladder cancer, breast
cancer, ovarian cancer, digestive tract tumors.
Squamous cell carcinoma antigen (SCCA)—cervical cancer, lung
cancer, head and neck cancer, nasopharyngeal cancer.
• Enzyme Tumor Markers
They are widely used for tumor treatment and prognosis monitoring because of their high
sensitivity and low specificity.
Alkaline phosphatase (ALP)—liver cancer, bone cancer, leukemia, sarcoma.
Lactate dehydrogenase (LDH)—liver cancer, lymphoma, leukemia, ovarian cancer.
Neuron-specific enolase (NSE)—small cell lung cancer, neuroblastoma, carcinoid, melanoma,
pancreatic cancer.
Prostate specific antigen (PSA)—prostate cancer.
α-L-fucosidase (AFU)—primary liver cancer.
• Protein Tumor Markers
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Tumor Markers
in Cancer Screening
9. ◆ Does the rise in tumor markers mean the
presence of cancer?
First of all, we must perform comprehensive
detections before confirming a diagnostic cancer,
through the methods of X-ray detection, CT detection,
B-ultrasound detection, and pathological diagnosis.
Since most tumor markers are not absolute specific
products of malignant tumors, it is possible that false
positives are in the detection of tumor markers.
Elevated tumor markers are not the same as detecting
cancer cells. Instead of indicating the presence of
cancer, their presence may be caused by certain
benign diseases or drugs.
Many factors might be the reasons for the rise of
tumor markers. For example, some benign
inflammatory diseases will increase the amount of
tumor markers.
CA125 may also be elevated in benign, borderline
tumors and endometriosis of the ovary.
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Tumor Markers
in Cancer Screening
10. ◆ Can tumor markers be used in cancer screening?
As some tumors do not secrete related proteins, and some tumor tissues have poor blood
circulation, the tumor markers produced by them cannot be secreted into peripheral
blood, which may lead to "false negatives" in tumor marker detection. If the tumor
marker is normal, the probability of suffering from a related malignancy is relatively low.
However, it needs to be reviewed regularly and diagnosed with other tests if the people
have related family history, precancerous lesions or symptoms. In short, reasonable
application and timely monitoring are the correct ways to clinically apply tumor markers.
◆ Is it necessary to detect tumor markers?
Although tumor markers are not accurate enough, they can help doctors with the
diagnosis, classification, prognosis, and treatment of tumors. It is not recommended to
do tumor marker testing screening for asymptomatic populations, but high-risk groups
should do screening once a year. Such as:
1. 45 years of age or older.
2. People with a genetic history of the tumor family, such as parents or grandparents in
a family who have had cancer.
3. People with long-term inflammatory diseases.
4. People engaged in certain special occupations, such as frequent exposure to
radioactive materials, toxic substances, or serious pollution in the working
environment.
5. People with long-term bad habits, such as smoking, drinking, long-term staying up
late or stressful.
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Tumor Markers
in Cancer Screening
11. ◆ How to choose tumor markers?
Most of single tumor markers cannot meet the clinical needs because of low sensitivity
or specificity. In order to improve the value of auxiliary diagnosis and therapeutic
monitoring of tumor markers, it is possible to select 2 or 3 complementary TMs for joint
detection after scientific analysis and strict screening.
Cancer Preferred indicators Auxiliary indicators
Colorectal cancer CEA, CA24-2 CA19-9
Pancreatic cancer CA19-9 CEA, CA24-2
Gastric cancer TCA72-4 CEA, CA19-9
Esophageal cancer CEA CA19-9, SCC
Liver cancer AFP AFU, CEA, CA19-9, HCG
Bile duct / gallbladder
carcinoma
CA19-9 CEA, CA24-2
Breast cancer HER2, CA15-3 CEA, CA125
Cervical cancer SCC CEA, CA125
Small Cell Lung Cancer NSE, ProGRP
Prostate cancer PSA
Bladder Cancer TPA, CEA, CA19-9 CYFRA21-1
Thyroid cancer Tg CEA
Malignant melanoma S100
Combined detection of tumor markers
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Tumor Markers
in Cancer Screening
12. Tumor Markers
in Cancer Screening
Featured antibodies for tumor markers
Targets Clone Applications Species Reactivity Cat.
CEA 161 ELISA, IP, WB Human CBMAB-XB0225-YC
CA19-9 SPM588 FC, IHC-P, IF Human CBMAB-C1123-CQ
CA19-9 CA19.9/1390R FC, IF, IHC-P Human CBMAB-C0512-CQ
CA19-9 CBXC-2378 FC, IF, IHC-P Human CBMAB-C0012-CQ
KLK3 IHC654 IHC-P, ELISA, IHC Human CBMAB-MA133-YC
KLK3 D2A8 WB, IP, IF (ICC) Human CBMAB-CP2096-LY
AFP IHC510 IHC Human CBMAB-MA007-YC
AFP 4G2D2 ELISA, IHC Human CBMAB-R4290-CN
AFP CBYC-A407 ELISA, WB, IHC-P Human CBMAB-A1569-YC
S100 IHC100 IHC-P, ELISA, IHC Human CBMAB-MA214-YC
CYFRA21-1 CBCNC-543 ELISA, WB Human CBMAB-C3276-CN
CYFRA21-1 KS19.1 ELISA, WB Human CBMAB-C3275-CN
hCG IHC593 IHC Human CBMAB-MA113-YC
CGB NYRhCG ELISA Human CBMAB-C10939-LY
CGA HCG 205 ICC, IHC Human CBMAB-C3841-CQ
ERBB2 44E6 WB Human, Mouse, Rat CBMAB-CP0937-LY
ERBB2 D8F12 WB, IHC-P Human, Mouse, Rat CBMAB-CP0935-LY
ERBB2 4C10 WB, ELISA Human CBMAB-A2684-LY
MUC16 IHC125 IHC-P, ELISA, IHC Human CBMAB-MA173-YC
MUC16 OV185-1 ICC, IF, IHC-P Human CBMAB-C12102-LY
ENO2 D20H2 WB, IP
Human, Mouse, Rat,
Monkey
CBMAB-CP0592-LY
ENO2 1A3 WB, ELISA Human CBMAB-A2614-LY
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13. Since 2004, Creative Biolabs has been working
on the development of tumor markers and the
production of antibodies against tumor markers.
At Creative Biolabs, we utilize advanced
antibody research tools, professional technical
support, and rapid global delivery to ensure
quality for scientific research workers and
customers in industry. We believe that to build
up a custom-service-centered business model is
crucial for optimizing the drug development
process, leveraging accessible resources, and
gathering a team from various backgrounds to
conduct drug discovery projects in the future.
As a preferred supplier for global customers,
we are confident to provide you with first-class
services covering a full range of applications. If
you have any need for antibodies,
please contact us.
• About us
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Tumor Markers
in Cancer Screening
14. Tel: 1-631-381-2994
Fax: 1-631-207-8356
45-1 Ramsey Road, Shirley, NY 11967, USA
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