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关于两种致癌基因在遗传性结肠癌易感性中作用的一项试验。

A test of the role of two oncogenes in inherited predisposition to colon cancer.

作者信息

Barker D, McCoy M, Weinberg R, Goldfarb M, Wigler M, Burt R, Gardner E, White R

出版信息

Mol Biol Med. 1983 Sep;1(2):199-206.

PMID:6594558
Abstract

Inheritance of mutationally altered oncogenes could predispose individuals to the development of specific tumors and account for familial tumor phenotypes. Using adjacent DNA sequence polymorphisms as genetic markers, we have examined two oncogenes, the Kirsten ras2, isolated from a human colon cancer cell line, and the Harvey ras1, isolated from a human bladder cancer cell line, for their role in the genetic etiology of inherited colon cancer in Gardner syndrome. Both oncogene loci have been shown to be unlinked to the Gardner syndrome locus and are, therefore, eliminated as candidates for the Gardner syndrome gene.

摘要

突变改变的癌基因的遗传可能使个体易患特定肿瘤,并解释家族性肿瘤表型。利用相邻的DNA序列多态性作为遗传标记,我们研究了两个癌基因,从人结肠癌细胞系中分离出的 Kirsten ras2 和从人膀胱癌细胞系中分离出的 Harvey ras1,它们在加德纳综合征遗传性结肠癌的遗传病因学中的作用。已证明这两个癌基因位点与加德纳综合征位点不连锁,因此,它们被排除作为加德纳综合征基因的候选基因。

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