Mismatch repair defects in cancer

被引:214
作者
Jiricny, J
Nyström-Lahti, M
机构
[1] Univ Zurich, Inst Med Radiobiol, CH-8008 Zurich, Switzerland
[2] Paul Scherrer Inst, CH-8008 Zurich, Switzerland
关键词
D O I
10.1016/S0959-437X(00)00066-6
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Post-replicative mismatch repair in humans utilises the hMSH2, hMSH6, hMSH3, hMLH1 and hPMS2 genes and possibly the newly identified hMLH3 gene. Recently, a link has been established between hMSH6 mutations and 'atypical' hereditary non-polyposis colon cancer (HNPCC) with an increased incidence of endometrial cancers. To satisfy the need for a diagnostic test capable of differentiating between pathogenic mutations and polymorphisms, several functional assays that fulfil these criteria have been described. These should allow for better diagnosis of HNPCC.
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页码:157 / 161
页数:5
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