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年轻头颈鳞状细胞癌患者中微卫星不稳定性的高频率:错配修复基因hMLH1和hMSH2未受累

High frequency of microsatellite instability in young patients with head-and-neck squamous-cell carcinoma: lack of involvement of the mismatch repair genes hMLH1 AND hMSH2.

作者信息

Wang Y, Irish J, MacMillan C, Brown D, Xuan Y, Boyington C, Gullane P, Kamel-Reid S

机构信息

Department of Cellular and Molecular Biology, Ontario Cancer Institute, University Health Network, Toronto, Ontario, Canada.

出版信息

Int J Cancer. 2001 Aug 1;93(3):353-60. doi: 10.1002/ijc.1337.

DOI:10.1002/ijc.1337
PMID:11433399
Abstract

The most prevalent risk factors in the development of head-and-neck squamous-cell carcinoma (HNSCC) are excessive tobacco and alcohol consumption. In young patients with HNSCC, these risk factors are often absent. Our purpose was to investigate the risk factors, microsatellite instability (MSI) changes and status of the mismatch repair genes hMLH1 and hMSH2 in a cohort of young patients with HNSCC. Fifty-seven HNSCC tumors were examined for the presence of MSI at 16 microsatellite sites using PCR. In the young patient group (24 cases, < or = 44 years old), 100% of tumors had MSI at 1 site at least and 88% had MSI at 2 or more loci. In older patients (33 cases, > or = 45 years), MSI at 1 or more sites was found in 61% of tumors (young vs. old, p = 0.0003) and instability at 2 or more sites was found in 36% of tumors (young vs. old, p = 0.0001). The involvement of the mismatch repair genes was investigated by examining promoter methylation, exon mutation and gene expression of hMLH1 and hMSH2. All results were negative, indicating that inactivation of these 2 genes does not play a role in the development of MSI in tumors from this patient group. Furthermore, the young patient group had a significantly lower incidence of smoking (46% young, 88% old; p = 0.001) and alcohol consumption (33% young, 67% old; p = 0.0169), emphasizing the probable importance of other environmental and/or genetic factors in the development of their disease.

摘要

头颈部鳞状细胞癌(HNSCC)发生过程中最常见的风险因素是过度吸烟和饮酒。在年轻的HNSCC患者中,这些风险因素往往不存在。我们的目的是调查一组年轻HNSCC患者的风险因素、微卫星不稳定性(MSI)变化以及错配修复基因hMLH1和hMSH2的状态。使用聚合酶链反应(PCR)检测了57例HNSCC肿瘤在16个微卫星位点的MSI情况。在年轻患者组(24例,年龄≤44岁)中,100%的肿瘤至少在1个位点存在MSI,88%的肿瘤在2个或更多位点存在MSI。在老年患者(33例,年龄≥45岁)中,61%的肿瘤在1个或更多位点存在MSI(年轻组与老年组相比,p = 0.0003),36%的肿瘤在2个或更多位点存在不稳定性(年轻组与老年组相比,p = 0.0001)。通过检测hMLH1和hMSH2的启动子甲基化、外显子突变和基因表达来研究错配修复基因的参与情况。所有结果均为阴性,表明这两个基因的失活在该患者组肿瘤的MSI发生过程中不起作用。此外,年轻患者组吸烟(年轻组46%,老年组88%;p = 0.001)和饮酒(年轻组33%,老年组67%;p = 0.0169)的发生率显著较低,这强调了其他环境和/或遗传因素在其疾病发生过程中的可能重要性。

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