Microsatellite instability in young patients with sporadic colorectal adenomas.

微卫星不稳定性 内科学 结直肠癌 种系突变 胃肠病学 生殖系 DNA错配修复 医学 腺瘤 肿瘤科 DNA甲基化 甲基化 微卫星 基因 突变 生物 癌症 遗传学 等位基因 基因表达
作者
Sung Keun Park,Dong Il Park,Sungha Park,Jung Ho Park,Hong Joo Kim,Yong Kyun Cho,Chong Il Sohn,Woo Kyu Jeon,Byung Ik Kim,Minkyung Kim,Jeong‐Seon Ji,Seon Ja Park,Dong Soo Han
出处
期刊:PubMed 卷期号:58 (110-111): 1531-7 被引量:5
标识
DOI:10.5754/hge09608
摘要

This study was designed to determine the prevalence of microsatellite instability (MSI) among colorectal adenomas detected in patients ≤ 40 years of age and to compare the prevalence of MSI in young (≤ 40 years) and older (>40 years) patients with colorectal adenomas. Additionally, we attempted to identify the underlying cause of MSI in these patients.We prospectively tested for the presence of MSI using five NCI markers in samples from the two patient groups. The frequency of MSI was compared and the underlying causes of MSI were determined by methylation specific PCR and germ-line mutation analysis for mismatch repair genes.The frequency of MSI was higher in the ≤ 40 group than the >40 group (31.4% and 6.4%, respectively, p=0.0004). The MSI-high pattern was also more prevalent in the ≤ 40 group than the >40 group (15.7% and 2.5%, respectively, p=0.014). The hypermethylated hMLH1 gene was demonstrated in 7/8 (87.5%) patients with MSI-high in the ≤ 40 group and in 1/2 (50.0%) patients with MSI-high in the >40 group. No study subject showed a germline mutation of hMLH1 or hMSH2.MSI-high was more frequent in young (≤ 40 years) patients with colorectal adenoma than in older (>40 years) patients. Hypermethylation of the hMLH1 gene appears to be an important cause of MSI-high in these patients.

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