Fearnhead Nicola S, Wilding Jennifer L, Bodmer Walter F
Cancer Research UK, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, Oxford OX3 9DZ, UK.
Br Med Bull. 2002;64:27-43. doi: 10.1093/bmb/64.1.27.
Familial adenomatous polyposis and hereditary non-polyposis colorectal cancer are dominantly inherited conditions with 100% and 80% life-time risk of developing colorectal cancer, respectively. The genetic mutations responsible for these two conditions lie in the adenomatous polyposis coli (APC) and mismatch repair genes. These same genes also play a key role in the formation of sporadic colorectal cancers, which arise on a background of a similar spectrum of mutations to the hereditary cancers. This article examines the genetic mechanisms underlying the hereditary colorectal cancers, as well as genetic predisposition to colorectal cancer in the general population in the absence of a clear-cut genetic syndrome. Colorectal cancer arises as the cumulative effect of multiple mutations within the cell, allowing it to escape growth and regulatory control mechanisms. This step-wise progression of mutations facilitates the histological transition from normal mucosa to adenoma to carcinoma. The latter part of this paper focuses on the key genetic events underlying this process and provides an overview of the genetic mechanisms responsible for colorectal tumorigenesis.
家族性腺瘤性息肉病和遗传性非息肉病性结直肠癌是显性遗传疾病,患结直肠癌的终生风险分别为100%和80%。导致这两种疾病的基因突变分别位于腺瘤性息肉病基因(APC)和错配修复基因中。同样这些基因在散发性结直肠癌的形成中也起着关键作用,散发性结直肠癌是在与遗传性癌症相似的一系列突变背景下发生的。本文探讨了遗传性结直肠癌的遗传机制,以及在没有明确遗传综合征的普通人群中患结直肠癌的遗传易感性。结直肠癌是细胞内多个突变的累积效应导致的,使其能够逃避生长和调控控制机制。这种逐步的突变进程促进了从正常黏膜到腺瘤再到癌的组织学转变。本文后半部分重点关注这一过程背后的关键遗传事件,并概述了结直肠癌发生的遗传机制。