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错配修复基因的剪接位点突变与普通人群患癌风险。

Splice site mutations in mismatch repair genes and risk of cancer in the general population.

机构信息

Department of Clinical Biochemistry, Herlev Hospital, Copenhagen University Hospital, Herlev Ringvej 75, 2730, Herlev, Denmark.

出版信息

Fam Cancer. 2013 Sep;12(3):567-72. doi: 10.1007/s10689-013-9601-7.

Abstract

We tested the hypothesis that splice site variations in MSH2 and MLH1 are associated with increased risk of hereditary non-polyposis colorectal cancer (HNPCC) and of cancer in general in the general population. In a cohort of 154 HNPCC patients with sequenced MSH2 and MLH1, we identified four possible splice-site mutations, which we subsequently genotyped in more than 9,000 individuals from the general population. Allele frequencies in the general population were 0 % for 942+3A>T in MSH2, 0.05 % for 307-19A>G, 0.005 % for 1,667+(2-8)del(taaatca);ins(attt), and 4.4 % for 1039-8T>A in MLH1. Odds ratios for HNPCC in a case-control design were 419 (95 % CI: 53-18,900) for 942+3A>T in MSH2, 19 (5-72) for 307-19A>G, 194 (21-1,768) for 1,667+(2-8)del(taaatca); ins(attt), and 0.3 (0.1-0.7) for 1,039-8T>A in MLH1. In the general population, incidence rate ratios for 1,039-8T>A carriers versus noncarriers were 0.70 (0.51-0.96) for HNPCC-related cancers combined and 0.82 (0.71-0.94) for all cancers combined in a prospective design. The three rare mutations were associated with increased risk of HNPCC. In contrast, the more common 1,039-8T>A associated with a decreased risk of HNPCC, of HNPCC-related cancers and of all cancers combined in the general population. These findings are novel and important in the counseling of HNPCC patients and their relatives.

摘要

我们验证了这样一个假说,即 MSH2 和 MLH1 的剪接位点变异与遗传性非息肉病性结直肠癌(HNPCC)风险增加以及一般人群中癌症风险增加相关。在一组经过 MSH2 和 MLH1 测序的 154 名 HNPCC 患者中,我们发现了四个可能的剪接位点突变,随后在一般人群中的 9000 多人中进行了基因分型。一般人群中 MSH2 的 942+3A>T 的等位基因频率为 0%,307-19A>G 的为 0.05%,1,667+(2-8)del(taaatca);ins(attt) 的为 0.005%,MLH1 的 1039-8T>A 的为 4.4%。病例对照设计中 HNPCC 的比值比为 MSH2 的 942+3A>T 为 419(95%CI:53-18900),307-19A>G 的为 19(5-72),1,667+(2-8)del(taaatca);ins(attt) 的为 194(21-1768),MLH1 的 1039-8T>A 的为 0.3(0.1-0.7)。在一般人群中,1039-8T>A 携带者与非携带者的发病率比为 HNPCC 相关癌症的 0.70(0.51-0.96),前瞻性设计中所有癌症的 0.82(0.71-0.94)。这三种罕见突变与 HNPCC 风险增加相关。相比之下,更为常见的 1039-8T>A 与 HNPCC、HNPCC 相关癌症和一般人群中所有癌症的风险降低相关。这些发现对于 HNPCC 患者及其亲属的咨询具有新颖性和重要性。

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