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Colorectal cancer

KEGG ID: hsa05210

中文名称

结直肠癌

通路描述

结直肠癌(CRC)是西方国家的第二大癌症相关死亡原因。CRC 源于结肠上皮细胞,这是由于定义的原癌基因和肿瘤抑制基因(TSG)中遗传改变的积累所致。在散发性 CRC 进展中已识别出两种主要的基因组不稳定性机制。第一种,称为染色体不稳定性(CIN),涉及原癌基因(如 K-ras)激活和 TSG(如 p53、DCC/Smad4、APC)失活的系列遗传改变。第二种,称为微卫星不稳定性(MSI),是由于 DNA 错配修复基因 MLH1 和/或 MSH2 的启动子超甲基化导致其失活,以及编码微卫星基因(如转化生长因子受体 II,TGF-RII)和 BAX 的次级突变引起的。遗传综合征具有特定基因(如染色体 5q 上的肿瘤抑制基因 APC 在 FAP 中的突变、错配修复基因在 HNPCC 中的突变)的胚系突变。
英文描述
Colorectal cancer (CRC) is the second largest cause of cancer-related deaths in Western countries. CRC arises from the colorectal epithelium as a result of the accumulation of genetic alterations in defined oncogenes and tumour suppressor genes (TSG). Two major mechanisms of genomic instability have been identified in sporadic CRC progression. The first, known as chromosomal instability (CIN), results from a series of genetic changes that involve the activation of oncogenes such as K-ras and inactivation of TSG such as p53, DCC/Smad4, and APC. The second, known as microsatellite instability (MSI), results from inactivation of the DNA mismatch repair genes MLH1 and/or MSH2 by hypermethylation of their promoter, and secondary mutation of genes with coding microsatellites, such as transforming growth factor receptor II (TGF-RII) and BAX. Hereditary syndromes have germline mutations in specific genes (mutation in the tumour suppressor gene APC on chromosome 5q in FAP, mutated DNA mismatch repair genes in HNPCC).

所含基因

87 个基因