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遗传性非息肉病性结直肠癌的分子机制

Molecular mechanisms underlying hereditary nonpolyposis colorectal carcinoma.

作者信息

Rhyu M S

出版信息

J Natl Cancer Inst. 1996 Mar 6;88(5):240-51. doi: 10.1093/jnci/88.5.240.

Abstract

MutS and MutL are bacterial genes that have critical roles in DNA repair and recombination. Mutations in homologues of these genes cause hereditary nonpolyposis colorectal carcinoma and are implicated in some sporadic (nonhereditary) colorectal cancers. Molecular functions of these genes have been defined through extensive work in bacteria and yeast. This article reviews and explores molecular events that require MutS and MutL, including mismatch repair, homologous recombination, and gene conversion. The mechanisms of action of eukaryotic MutS and MutL homologues are compared with those of their prokaryotic counterparts, and the relevance of these mechanisms to tumorigenesis is discussed.

摘要

MutS和MutL是细菌基因,在DNA修复和重组中起关键作用。这些基因的同源物发生突变会导致遗传性非息肉病性结直肠癌,并与一些散发性(非遗传性)结直肠癌有关。通过在细菌和酵母中的大量研究,已经明确了这些基因的分子功能。本文回顾并探讨了需要MutS和MutL参与的分子事件,包括错配修复、同源重组和基因转换。将真核生物MutS和MutL同源物的作用机制与其原核生物对应物的机制进行了比较,并讨论了这些机制与肿瘤发生的相关性。

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