Zhao Ya-shuang, Hu Fu-lan, Wang Fan, Han Bing, Li Dan-dan, Li Xiang-wei, Zhu Sui
Department of Epidemiology, Public Health College, Harbin Medical University, Heilongjiang Province, People's Republic of China.
J Toxicol Environ Health A. 2009;72(11-12):690-7. doi: 10.1080/15287390902841003.
Studies on mutations and mutation frequencies of the MSH6 gene, which mainly focus on new types of mutations in small samples, have been published ever since the first report of MSH6 mutation in two atypical hereditary non-polyposis colorectal cancer patients. However, the results remain inconsistent. Therefore, a systematic review was conducted and a meta-analysis was undertaken to determine the frequency of MSH6 mutation in colorectal and endometrial cancers. From 27 studies, 180 cases with MSH6 mutation in a total of 3196 cases were detected. In colorectal and endometrial cancers the MSH6 mutation frequency is 7.2 and 9.6%, respectively. MSH6 mutation frequency was 10.4% in hereditary non-polyposis colorectal cancer patients, 7.1% in atypical hereditary non-polyposis colorectal cancer patients, and 5.9% in sporadic patients. The frequency of MSH6 mutation in high microsatellite instability (MSI-H) was 11.6% and in low microsatellite instability (MSI-L) cases was (13.3%), which were higher than in microsatellite stability (MSS) cases (1.7%). The mean age of the earliest onset of colorectal and endometrial cancers in MSH6 mutation carriers was 51.2 and 56.5 yr, respectively. Data suggest that the frequency of MSH6 mutation is higher in hereditary non-polyposis colorectal cancer patients than in atypical hereditary non-polyposis colorectal cancer and sporadic patients. MSH6 mutation frequency was also higher in endometrial than colorectal cancers. The mean age of earliest onset of endometrial cancer (56.5 yr) is older than for colorectal cancer (51.2 yr) in carriers of MSH6 mutation. Our results provide evidence for clinical genetic testing and counseling.
自首次报道两名非典型遗传性非息肉病性结直肠癌患者存在MSH6基因突变以来,针对MSH6基因的突变及突变频率的研究陆续发表,这些研究主要聚焦于小样本中的新型突变。然而,研究结果仍不一致。因此,我们进行了一项系统综述并开展荟萃分析,以确定结直肠癌和子宫内膜癌中MSH6基因突变的频率。在27项研究中,共检测了3196例病例,其中180例存在MSH6基因突变。在结直肠癌和子宫内膜癌中,MSH6基因突变频率分别为7.2%和9.6%。遗传性非息肉病性结直肠癌患者中MSH6基因突变频率为10.4%,非典型遗传性非息肉病性结直肠癌患者中为7.1%,散发性患者中为5.9%。高微卫星不稳定性(MSI-H)病例中MSH6基因突变频率为11.6%,低微卫星不稳定性(MSI-L)病例中为13.3%,均高于微卫星稳定(MSS)病例(1.7%)。MSH6基因突变携带者中,结直肠癌和子宫内膜癌最早发病的平均年龄分别为51.2岁和56.5岁。数据表明,遗传性非息肉病性结直肠癌患者中MSH6基因突变频率高于非典型遗传性非息肉病性结直肠癌患者和散发性患者。子宫内膜癌中MSH6基因突变频率也高于结直肠癌。MSH6基因突变携带者中,子宫内膜癌最早发病的平均年龄(56.5岁)高于结直肠癌(51.2岁)。我们的研究结果为临床基因检测和咨询提供了依据。