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散发性结直肠肿瘤中的APC突变:一个突变“热点”及“两次打击”的相互依赖性

APC mutations in sporadic colorectal tumors: A mutational "hotspot" and interdependence of the "two hits".

作者信息

Rowan A J, Lamlum H, Ilyas M, Wheeler J, Straub J, Papadopoulou A, Bicknell D, Bodmer W F, Tomlinson I P

机构信息

Molecular and Population Genetics Laboratory, Imperial Cancer Research Fund, 44 Lincoln's Inn Fields, London WC2A 3PX, United Kingdom.

出版信息

Proc Natl Acad Sci U S A. 2000 Mar 28;97(7):3352-7. doi: 10.1073/pnas.97.7.3352.

Abstract

Although APC mutations occur at a high frequency in colorectal cancers, few studies have performed a comprehensive analysis by screening the whole gene for mutations and assessing allelic loss. APC seems to act as a tumor-suppressor gene in a "nonclassical" fashion: data from familial adenomatous polyposis (FAP) show that the site of the germ-line mutation determines the type of "second hit" in FAP tumors, and simple protein inactivation is selected weakly, if at all. In this study, we screened the entire coding region of APC for mutations and assessed allelic loss in a set of 41 colorectal cancer cell lines. Of 41 cancers, 32 (83%) showed evidence of APC mutation and/or allelic loss. We identified several APC mutations and found a "hotspot" for somatic mutation in sporadic colorectal tumors at codon 1,554. Our results suggest that APC mutations occur in the great majority of colorectal cancers, the exceptions almost all being RER+ tumors, which may substitute for altered APC function by mutations in beta-catenin and/or at other loci. When combined with previously published data, our results show that there is interdependence of the "two hits" at APC in sporadic colorectal tumors as well as in FAP. APC mutations in the "mutation cluster region," especially those close to codon 1,300, are associated with allelic loss, whereas tumors with mutations outside this region tend to harbor truncating mutations. The causes of this phenomenon are probably selection for retained N-terminal and lost C-terminal APC functions, effects on beta-catenin levels, and APC protein stability.

摘要

尽管APC突变在结直肠癌中出现的频率很高,但很少有研究通过筛选整个基因的突变并评估等位基因缺失来进行全面分析。APC似乎以一种“非经典”方式发挥肿瘤抑制基因的作用:家族性腺瘤性息肉病(FAP)的数据表明,种系突变的位点决定了FAP肿瘤中“第二次打击”的类型,而且简单的蛋白质失活即使被选择也是微弱的。在本研究中,我们筛选了APC的整个编码区以寻找突变,并评估了一组41个结直肠癌细胞系中的等位基因缺失情况。在41例癌症中,32例(83%)显示有APC突变和/或等位基因缺失的证据。我们鉴定出了几种APC突变,并在散发性结直肠肿瘤的第1554密码子处发现了一个体细胞突变“热点”。我们的结果表明,APC突变发生在绝大多数结直肠癌中,几乎所有例外都是RER +肿瘤,它们可能通过β-连环蛋白和/或其他位点的突变来替代改变的APC功能。当与先前发表的数据相结合时,我们的结果表明,在散发性结直肠肿瘤以及FAP中,APC的“两次打击”存在相互依赖性。“突变簇区域”中的APC突变,尤其是那些靠近第1300密码子的突变,与等位基因缺失相关,而该区域外有突变的肿瘤往往含有截短突变。这种现象的原因可能是对保留的N端和缺失的C端APC功能的选择、对β-连环蛋白水平的影响以及APC蛋白稳定性。

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