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Questions and Answers
What defines a tumor marker?
What defines a tumor marker?
Which characteristic is NOT a quality of a good tumor marker?
Which characteristic is NOT a quality of a good tumor marker?
In which locations can tumor markers be found?
In which locations can tumor markers be found?
What is an example of a carbohydrate epitope recognized by monoclonal antibodies?
What is an example of a carbohydrate epitope recognized by monoclonal antibodies?
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Why should the half-life of a tumor marker not be very long?
Why should the half-life of a tumor marker not be very long?
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How should the plasma level of a tumor marker correlate with tumor characteristics?
How should the plasma level of a tumor marker correlate with tumor characteristics?
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Which type of molecules can tumor markers be classified into?
Which type of molecules can tumor markers be classified into?
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What is the significance of tumor markers in cancer management?
What is the significance of tumor markers in cancer management?
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What is a primary requirement for a tumor marker to be used in screening asymptomatic individuals in the general population?
What is a primary requirement for a tumor marker to be used in screening asymptomatic individuals in the general population?
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Which of the following potential uses of tumor markers involves assessing treatment outcomes?
Which of the following potential uses of tumor markers involves assessing treatment outcomes?
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What is a significant limitation of most tumor markers when used for cancer screening?
What is a significant limitation of most tumor markers when used for cancer screening?
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In cancer diagnostics, what does a higher plasma level of a tumor marker generally indicate?
In cancer diagnostics, what does a higher plasma level of a tumor marker generally indicate?
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How can the serum level of a tumor marker serve as a prognostic indicator?
How can the serum level of a tumor marker serve as a prognostic indicator?
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What may the rate of decrease in a tumor marker's level after treatment indicate?
What may the rate of decrease in a tumor marker's level after treatment indicate?
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Which of the following is true regarding the specificity of tumor markers?
Which of the following is true regarding the specificity of tumor markers?
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What clinical utility does quantifying tumor markers provide?
What clinical utility does quantifying tumor markers provide?
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What does an increase in alkaline phosphatase (ALP) usually indicate?
What does an increase in alkaline phosphatase (ALP) usually indicate?
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Which enzyme has largely replaced prostatic acid phosphatase (PAP) in clinical use for prostate cancer?
Which enzyme has largely replaced prostatic acid phosphatase (PAP) in clinical use for prostate cancer?
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What is the significance of the ratio between free and total prostate specific antigen (PSA)?
What is the significance of the ratio between free and total prostate specific antigen (PSA)?
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What protocols are recommended for accurate cancer diagnosis when using PSA testing?
What protocols are recommended for accurate cancer diagnosis when using PSA testing?
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How often should the PSA level fall below the detection limit after treatment monitoring?
How often should the PSA level fall below the detection limit after treatment monitoring?
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What are potential causes of increased PSA levels in serum that are not cancer-related?
What are potential causes of increased PSA levels in serum that are not cancer-related?
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Which condition can potentially elevate prostatic acid phosphatase (PAP) levels despite having a benign nature?
Which condition can potentially elevate prostatic acid phosphatase (PAP) levels despite having a benign nature?
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What is a primary use of serum PSA levels in prostate cancer management?
What is a primary use of serum PSA levels in prostate cancer management?
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What is the primary utility of AFP and hCG in relation to germ cell tumors?
What is the primary utility of AFP and hCG in relation to germ cell tumors?
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Which of the following cancers is not typically monitored using CEA levels?
Which of the following cancers is not typically monitored using CEA levels?
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What does an elevated CA 15-3 level indicate?
What does an elevated CA 15-3 level indicate?
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Why should CEA not be used as a screening tool?
Why should CEA not be used as a screening tool?
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What types of cancer are indicated by CA 125 levels?
What types of cancer are indicated by CA 125 levels?
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How accurate is CA 125 for detecting recurrence of ovarian cancer?
How accurate is CA 125 for detecting recurrence of ovarian cancer?
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In patients with ovarian masses, what indication does a CA 125 level of less than 65 kU/L provide?
In patients with ovarian masses, what indication does a CA 125 level of less than 65 kU/L provide?
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What are carbohydrate markers primarily associated with?
What are carbohydrate markers primarily associated with?
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Which cancer types are associated with elevated levels of CA 19-9?
Which cancer types are associated with elevated levels of CA 19-9?
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What is the role of β2-microglobulin as a protein marker?
What is the role of β2-microglobulin as a protein marker?
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Which condition can be identified by monitoring CA 19-9 levels?
Which condition can be identified by monitoring CA 19-9 levels?
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What does a positive estrogen receptor indicate in breast cancer treatment?
What does a positive estrogen receptor indicate in breast cancer treatment?
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Ferritin is a marker for which of the following cancers?
Ferritin is a marker for which of the following cancers?
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What is the significance of Bence-Jones protein in medical diagnosis?
What is the significance of Bence-Jones protein in medical diagnosis?
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In patients with negative estrogen and progesterone receptors, what is the likely treatment approach?
In patients with negative estrogen and progesterone receptors, what is the likely treatment approach?
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Which protein markers are among the most reliable for cancer diagnosis?
Which protein markers are among the most reliable for cancer diagnosis?
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What percentage of patients with estrogen receptor (+) tumors typically respond to hormonal therapy?
What percentage of patients with estrogen receptor (+) tumors typically respond to hormonal therapy?
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Which type of receptor testing is considered useful as an adjunct to estrogen receptor testing?
Which type of receptor testing is considered useful as an adjunct to estrogen receptor testing?
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What is the role of the C-erbB2 (HER-2 Neu) receptor in relation to epidermal growth factor (EGF)?
What is the role of the C-erbB2 (HER-2 Neu) receptor in relation to epidermal growth factor (EGF)?
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Which class of genes is responsible for the normal regulation of cell growth and differentiation?
Which class of genes is responsible for the normal regulation of cell growth and differentiation?
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Mutations in which of the following genes are specifically correlated with an inherited predisposition to breast and ovarian cancer?
Mutations in which of the following genes are specifically correlated with an inherited predisposition to breast and ovarian cancer?
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What effect do alterations in tumor suppressor genes have on tumor development?
What effect do alterations in tumor suppressor genes have on tumor development?
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Which of the following is NOT a type of gene implicated in the development of cancer?
Which of the following is NOT a type of gene implicated in the development of cancer?
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Which of these mutations are correlated with acute myeloid leukemia and neuroblastoma?
Which of these mutations are correlated with acute myeloid leukemia and neuroblastoma?
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Study Notes
Cancer & Tumor Markers
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Tumor markers are biochemical substances (hormones, enzymes, proteins) produced by cancer cells or the body's response to cancer.
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Symptoms of cancer vary depending on the type but general symptoms include fatigue, weight loss, pain, skin changes, unusual bleeding, persistent cough, and fever.
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Treatment options include chemotherapy, radiation, and surgery.
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Benign tumors are non-cancerous, while malignant tumors are cancerous and can spread to other tissues and organs.
Types of Cancer
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Common cancer types (according to the National Cancer Institute) include bladder, lung, breast, melanoma, endometrial, kidney cancer, leukemia, lymphoma, pancreatic, prostate, colon and rectal cancers.
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A diagram shows an example of primary cancers and areas they might metastasize (spread) to, including the brain, lungs, skin, and pancreas.
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The most common cancers in men include prostate, lung, and colorectal cancer.
- For women: breast, lung, and colorectal cancer
- For children: leukemia, brain tumors, and lymphoma
Types of Cancers - Classification
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Carcinoma: Starts in the skin or tissues lining internal organs (e.g., skin, lung, colon, pancreas). Subtypes include adenocarcinoma, basal cell carcinoma, squamous cell carcinoma, and transitional cell carcinoma.
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Sarcoma: Begins in bone, cartilage, or other connective tissue. This includes bone sarcomas and soft tissue sarcomas.
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Leukemia: Starts in blood-forming tissue, causing abnormal blood cells to enter the bloodstream. Ages of onset include 0-5, 14-18, 19-40, and 60+. Subtypes include lymphoblastic leukemia and T-cell leukemia.
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Lymphoma & Myeloma: Starts in white blood cells, affecting lymph nodes. The tissue sites it affects can include the stomach, brain, and intestines. Subtypes include B-cell lymphocytes and T-cell lymphocytes. -Myeloma develops in plasma cells, is a blood cancer, and can damage bones, kidneys, and the red blood cell count.
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Central Nervous System Cancers: Start in brain tissue and spinal cord. The brain controls the body by sending electrical signals along nerve fibers, and the brain and spinal cord form the central nervous system.
Normal vs. Cancerous Cells
- Normal cells divide and go through apoptosis (cell death) when damaged. Cancer cells multiply constantly, have an altered nucleus structure, irregular shapes, and lack defined boundaries in groups.
Role of Cell Division in Cancer
- Benign tumors do not spread
- Malignant tumors invade surrounding tissues.
- Cancer cells may break off and form new tumors (metastasis).
Spread of Cancer
- Primary cancer starts at a site in the body. It may spread (metastasize) to other parts of the body.
- Secondary cancers form from the spread of primary cancer.
Spread to Other Areas of Body
- Cancer cells can spread through blood vessels (capillaries) and the lymphatic system.
- Circulation tumor cells may get lodged in small blood vessels, move through capillary walls, and form new tumors in other organs.
###Properties of Cancer Cells
- Cancer cells display uncontrolled cell division leading to tumor formation.
- They have decreased cell adhesion.
- They show diverse genetic alterations.
- Cancer cells lack differentiation to normal cell characteristics.
- They lose the ability to communicate with other cells.
- They lose sensitivity, adhesion molecules.
Tumor Markers- Properties
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Tumor markers should be present in or produced by the tumor itself.
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Tumor markers should not be present in healthy tissues.
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Tumor marker levels need to be minimal in healthy subjects and benign conditions.
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Tumor markers should be specific to a tissue and have different immunological properties from those produced elsewhere in the body.
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Plasma marker levels are proportional to the tumor's size and activity.
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Tumor marker half-lives should not be excessively prolonged.
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Tumor markers should be detectable even in small tumors.
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Tumor markers are helpful in predicting recurrence.
Classification of Tumor Markers
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They are classified by molecular type. This includes enzymes/isoenzymes, hormones, oncofetal antigens, carbohydrate epitopes recognized by monoclonal antibodies, and receptors.
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Specific examples of tumor markers by type are provided for some common types of cancer.
Potential Uses of Tumor Markers
- Screening the general population.
- Diagnosing symptomatic patients.
- Clinically staging cancer.
- Estimating tumor volume.
- Prognostic indicator of disease progression.
- Evaluating the success of treatment. detecting recurrence of cancer.
- Monitoring response to therapy
- Radioimmunolocalization of tumor masses.
Tumor Marker Considerations
- Most tumor markers are not specific for singular tumors, but are found in multiple tumor types.
- Tumor markers are typically present in higher quantities in cancer patients' blood versus healthy subjects or those with benign diseases.
- Some tumor markers are proportionate to tumor size, while others reflect activity.
- The clinical staging of cancer can be assisted by tumor marker quantification.
- Serum levels reflect tumor burden and prognostic indicators of disease progression and survival.
- The response to therapies are often indicated by drops in tumor markers. Recurrence is often indicated by an increase in marker.
Specific Tumor Markers — Examples
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Enzymes: Alkaline phosphatase (ALP) and Prostatic acid phosphatase (PAP). Increased levels associated with liver cancer, bone/liver metastatic cancer or other malignancies like ovarian, lung cancers. PAP is used to stage prostate cancer & monitor treatment.
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PSA: Prostate-specific antigen. Used for prostate cancer—it's highly specific to it during early cancer.
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Hormones: Calcitonin. High levels are usually associated with medullary thyroid cancer and can correlate with tumor volume and metastasis.
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Oncofetal Antigens: a-fetoprotein (AFP) and carcinoembryonic antigen (CEA). AFP is useful for screening and diagnosing hepatocellular carcinoma, pregnancy and chronic liver disease. CEA is a marker for colorectal, lung, and breast cancers.
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Carbohydrate Markers: CA 15-3, CA 125, CA 19-9. CA 15-3 is correlated with breast cancer. CA 125 is linked to ovarian/endometrial cancers and detecting residual disease. CA 19-9 is a marker for pancreatic and colorectal cancers.
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Protein Markers: β2-microglobulin, ferritin, thyroglobulin, Immunoglobulins (including monoclonal paraproteins and Bence-Jones protein). β2-microglobulin links to multiple myeloma, Hodgkin lymphoma. Ferritin is a marker for Hodgkin lymphoma, leukemia, liver, lung, and breast cancers. Thyroglobulin helps detect differentiated thyroid cancer. Immunoglobulins/Bence-Jones are markers for multiple myeloma.
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Receptor Markers: Estrogen and progesterone receptors in breast cancer are used for hormonal therapies. Measuring cytoplasmic receptors are crucial.
Genetic Changes
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Proto-oncogenes, tumor suppressor genes, apoptosis-related genes, and DNA repair genes are related to cancer development.
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These genetic changes are linked to chronic myeloid leukemia, neuroblastoma, acute myeloid leukemia ,breast and ovarian cancers, and colorectal cancers, and other types.
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Genes are implicated in normal cell growth and differentiation, regulating apoptosis (programmed cell death), and DNA repair.
Chromosomal Translocations
- Translocations involve chromosomes exchanging segments. One example is the c-myc gene translocation in Burkitt's lymphoma. Also, translocations in chromosomes 9 and 22 are associated with chronic myeloid leukemia.
Conclusion
- Tumor markers assist in cancer diagnosis, staging, prognosis, and monitoring treatment success.
- However, because tumor markers are not always specific to a single tumor type, and some conditions other than cancer can produce these markers, additional testing is often necessary to clarify diagnostic and staging findings.
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Description
This quiz explores the essential characteristics and significance of tumor markers in cancer diagnostics and management. Questions cover their classification, uses, and limitations, providing a comprehensive understanding of their role in screening and treatment outcomes. Test your knowledge and see how well you understand tumor markers!