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Cancer Health Center

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Genetics of Colorectal Cancer (PDQ®): Genetics - Health Professional Information [NCI] - Colon Cancer Genes

Major Genes

Major genes are defined as those that are necessary and sufficient for disease causation, with important mutations (e.g., nonsense, missense, frameshift) of the gene as causal mechanisms. Major genes are typically considered those that are involved in single-gene disorders, and the diseases caused by major genes are often relatively rare. Most pathogenic mutations in major genes lead to a very high risk of disease, and environmental contributions are often difficult to recognize.[1] Historically, most major colon cancer susceptibility genes have been identified by linkage analysis using high-risk families; thus, these criteria were fulfilled by definition, as a consequence of the study design.

The functions of the major colon cancer genes have been reasonably well characterized over the past decade. Three proposed classes of colon cancer genes are tumor suppressor genes, oncogenes, and DNA repair genes.[2] Tumor suppressor genes constitute the most important class of genes responsible for hereditary cancer syndromes and represent the class of genes responsible for both familial adenomatous polyposis (FAP) and juvenile polyposis syndrome (JPS), among others. Germline mutations of oncogenes are not an important cause of inherited susceptibility to colorectal cancer (CRC), even though somatic mutations in oncogenes are ubiquitous in virtually all forms of gastrointestinal cancers. Stability genes, especially the mismatch repair (MMR) genes responsible for Lynch syndrome (LS) (also called hereditary nonpolyposis colorectal cancer [HNPCC]), account for a substantial fraction of hereditary CRC, as noted below. (Refer to the Lynch syndrome [LS] section in the Major Genetic Syndromes section of this summary for more information). MYH is another important example of a stability gene that confers risk of CRC based on defective base excision repair. Table 2 summarizes the genes that confer a substantial risk of CRC, with their corresponding diseases.

Table 2. Genes Associated with a High Susceptibility of Colorectal Cancer

Gene Syndrome Hereditary Pattern Predominant Cancer
FAP = familial adenomatous polyposis; JPS = juvenile polyposis syndrome; LS = Lynch syndrome; OMIM = Online Mendelian Inheritance in Man database; PJS = Peutz-Jeghers syndrome.
Tumor suppressor genes
APC(OMIM) FAP Dominant Colon, intestine, etc.
TP53(p53) (OMIM) Li-Fraumeni Dominant Multiple (including colon)
STK11(LKB1) (OMIM) PJS Dominant Multiple (including intestine)
PTEN(OMIM) Cowden Dominant Multiple (including intestine)
BMPR1A(OMIM) JPS Dominant Gastrointestinal
SMAD4(MADH/DPC4) (OMIM) JPS Dominant Gastrointestinal
Repair/stability genes
MLH1(OMIM),MSH2(OMIM),MSH6(OMIM),PMS2 (OMIM) LS Dominant Multiple (including colon, uterus, and others)
EPCAM (TACSTD1) (OMIM) LS Dominant Multiple (including colon, uterus, and others)
MYH(MUTYH) (OMIM) MYH-associated polyposis Recessive Colon
POLD1(OMIM),POLE(OMIM) Oligopolyposis Dominant Colon, endometrial
1 | 2 | 3 | 4 | 5 | 6 | 7 | 8
1 | 2 | 3 | 4 | 5 | 6 | 7 | 8
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