Tumor markers
From WikiLectures
Tumor markers (tumor markers, TM) are laboratory detectable marks from which the tumor growth unwound (Proto-oncogenes, oncogenes, anti-oncogenes) or a malignancy which manifests itself (tumor antigens, umor cells or products of the reactive products of non-tumor cells).[1][2]
- in the narrower (clinical) sense of the word substances that can be determined in blood, urine or tissue and have a higher value in cancer
- use to refine diagnosis, monitor the course of therapy and detect early relapse
- they can also be elevated by non-tumor causes
- are not used as nationwide screening, only the PSA is used for screening of patients at risk for Ca prostate
- they can be produced directly by tumor cells or non-tumor cells in response to the presence of a tumor
- if the TM examination is performed at the appropriate choice and at reasonable intervals, it can be a good helper for the attending physician - determining the response to treatment, disease progression and the patient's prognosis
- tumor markers can be divided according to the site of production, specificity, chemical structure and biological character [3][4]
Tumor-specific tumor markers[edit | edit source]
- associated with the presence of certain tumor tissue
- due to the considerable overlap of TM production in different tumor tissues, the specificity is low
- suitable for monitoring remission of cancer and early diagnosis of disease relapse:
- eg CEA (Ca GITu), CA 19–9 (Pancreatic Cancer), CA 125 (ovarian cancer), etc.
Tissue-specific tumor markers[edit | edit source]
- rather related to a certain tissue in which a pathological event may take place (eg tumor growth)
- often increased from non-tumor causes (eg PSA in men - prostate; hCG a AFP – germinal liver tissue)[5][6]
Humoral[edit | edit source]
Abbreviation | Name | Physiologically produced | Standard | Increased at | False positivity | Note |
---|---|---|---|---|---|---|
CEA | carcinoembryonic antigen | epithelial cells during fetal development | <3 μg/l | ca colorectal, breast carcinoma, lung cancer, ovarian cancer, liver metastases, | Cirrhosis, GIT inflammation | |
AFP | α-fetoprotein | yolk sac and fetal liver | <10 μg/l | cirhosis, active hepatitis, nonseminomas, Germinal tumors (teratoma), hepatocellular carcinoma, hepatolastoma | pregnancy | |
CA 15-3 | Carcinoma antigen 15-3 | breast carcinoma, GIT tumors, glandular epithelial tumors | hepatopathy, cholangitis, lung disease, renal disorders, pregnancy | ↑ breast carcinoma – sensitivity 75%, specificity 90%, some GIT tumors | ||
MCA | mucinous carcinoma antigen | breast carcinoma | rise earlier than CA 15-3, use for confirmation at elevated CA 15-3 | |||
CA 19-9 | carbohydrate antigen | Pancreatic Cancer, stomach cancer, ca colorectal, breast carcinoma | obstructive jaundice | |||
CA 72-4 | carbohydrate antigen | stomach cancer, esophageal cancer, lung cancer, ovarian cancer | ||||
CA 125 | carbohydrate antigen | ovarian cancer | benign ovarian and endometrial conditions, hepatopathy, pancreatitis, pregnancy, menstruation | monitoring of ovarian ca treatment, screening in women with ovarian ca in family history | ||
SCC | squamous cell carcinoma antigen | squamous cell carcinomas | ||||
TPA/S | tissue polypeptide antigen | cell proliferation | various cancers (cancer of the bladder, head and neck) | mixture of about 20 cytokeratins, increases in proportion to the growing tumor | ||
CYFRA 21-1 | cytokeratin fragments 19 | non-small cell lung cancer | ||||
PSA | prostate specific antigen | into the seminal vesicle fluid to liquefy ejaculate by prostate cells | <2,5 μg/l < 50 let <5 μg/l 50–60 let 8,5< μg/l > 60 let |
Ca prostate | ejaculation, per rectum examination before collection, BPH | values above 10 μg/l – 50% ca risk, about20 % ca prostate has PSA in the norm |
LD | lactate dehydrogenase | liver, myocardium, skeletal muscles, erythrocytes | 4,10 µkat/l | testicular tumors, leukemia, RCC, Hodgkin's lymphoma | ||
ALP | alkaline phosphatase | sarcoma, Prostatic Carcinoma | bile duct obstruction | |||
ACP | acid phosphatase | skeletal metastases, Prostatic Carcinoma | ||||
GGT | γ-glutamyltransferase | metastatic liver disease | alcoholics, bile duct obstruction | |||
NSE | neuron specifická enoláza | neuroblastoma, retinoblastoma, malignant melanoma, SCLC | hemolysis | in CNS tumors better determined in cerebrospinal fluid | ||
TK | thymidine kinase | leukemia, lymphoma, non-small cell lung ca. | DNA replacement synthesis route | |||
hCG | human chorionic gonadotropin | placenta | trophoblast tumors, choriokarcinoma (100% sensitivity), germinal tumors of the testes and ovaries | pregnancy | screening of endangered persons, examination of the β-subunit | |
PRL | prolactin | during pregnancy and after childbirth | prolactinoma, MEN I | slightly during physical exertion, mental stress | ||
CT | calcitonin | medullary thyroid carcinoma | ||||
Thyreoglobulin | thyreoglobulin | follicular carcinoma of the thyroid gland | ||||
Ferritin | ferritin | multiple myeloma, AML, Hodgkin's lymphoma | ||||
β2 microglobulin | β2 microglobulin | CLL, multiple myeloma, lymphomas | ||||
Paraprotein | paraprotein | multiple myeloma | Bence-Jones protein | |||
VMA | vanillic acid | catecholamine degradation product | functional tumors of the adrenal glands | determination in urine, or determination of metanephrines (plasma, urinary) | ||
HIAA | 5-hydroxyindoleacetic acid | serotonin degradation product | functional karcinoids | determination in urine |
Cell markers[edit | edit source]
Abbreviation | Name | Physiologically produced | Standard | Increased at | False positivity | Note |
---|---|---|---|---|---|---|
HER2/neu | breast cancer | target for monoclonal antibodies (Herceptin), increased expression = worse prognosis |
Genetic markers[edit | edit source]
Abbreviation | Name | Physiologically produced | Standard | Increased at | False positivity | Note |
---|---|---|---|---|---|---|
p53 | genome guardian | cell cycle regulation | Li-Fraumeni syndrome, sarcomas, breast cancer | |||
BRCA1/2 | breast cancer | breast and ovarian cancer |
References[edit | edit source]
References[edit | edit source]
- ↑ Tumor Markers - National Cancer Institute. [online].
- ↑ KALOUSOVÁ, Marta. Tumor Markers – Nádorové markery. [online].
- ↑ SCHNEIDERKA PETR. Kapitoly z klinické biochemie. 2., dopl. a přeprac. vyd. Praha: Karolinum, 2004, 365 s.
- ↑ PETRUŽELKA LUBOŠ a KONOPÁSEK BOHUSLAV. Klinická onkologie. 1. vyd. Praha: Karolinum, 2003, 274 s.
- ↑ PRŮŠA RICHARD. Orientační rozmezí hodnot biochemických a hematologických vyšetření podle věkových skupin. 1. vyd. Praha: Ústav klinické biochemie a patobiochemie 2. lékařské fakulty UK, 1999, 41 s.
- ↑ VALÍK, D, T ZIMA a O TOPOLČAN, et al. Doporučení České společnosti klinické biochemie (ČSKB ČLS JEP), České onkologické společnosti (ČOS ČLS JEP) a České společnosti nukleární medicíny (ČSNM ČLS JEP) k využití nádorových markerů v klinické praxi. [online].
Kategorie:Patobiochemie Kategorie:Vnitřní lékařství Kategorie:Chirurgie Kategorie:Onkologie Kategorie:Klinická biochemie