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Correlation between microsatellite instability and metachronous disease recurrence after endoscopic mucosal resection in patients with early stage gastric carcinoma

微卫星不稳定性 医学 免疫组织化学 胃肠病学 增殖细胞核抗原 阶段(地层学) 粘膜切除术 病理 内科学 DNA错配修复 癌症 内窥镜检查 微卫星 生物 结直肠癌 基因 古生物学 等位基因 生物化学
作者
Akira Kawamura,Kyoichi Adachi,Shunji Ishihara,Tomoko Katsube,Toshiharu Takashima,Mika Yuki,Kazutoshi Amano,Ryo Fukuda,Yukimasa Yamashita,Yoshikazu Kinoshita
出处
期刊:Cancer [Wiley]
卷期号:91 (2): 339-345 被引量:16
标识
DOI:10.1002/1097-0142(20010115)91:2<339::aid-cncr1007>3.0.co;2-2
摘要

Since endoscopic treatment was first evaluated and established as a treatment for patients with early stage gastric carcinoma, metachronous disease recurrence at other sites in the stomach after endoscopic treatment has become a major problem.A retrospective case-control study was conducted on 10 patients with metachronous recurrence of gastric carcinoma after undergoing successful endoscopic mucosal resection (EMR) therapy for early stage gastric carcinoma and on 14 patients without recurrence. Gastric mucosal tissues obtained during the initial EMR were dissected, and DNA samples from the tumor tissue and surrounding nonneoplastic mucosa were extracted separately. Microsatellite instability (MSI) was tested in five microsatellite markers (D2S137, D3S1067, TP53, TGFbetaRII, and BAX). The authors also looked for K-ras codon 12 point mutations in the tumor tissues. In addition, immunohistochemical staining was done to test for the presence of proliferating cell nuclear antigen (PCNA), p53, hMSH2, and hMLH1 in the mucosal tissues. Finally, the correlation between the presence or absence of metachronous recurrence and the characteristics of the primary tumor (MSI, K-ras, p53, etc.) were investigated.Three of 10 patients with recurrent disease showed MSI in more than two microsatellite markers among 3-5 investigated site (MSI-H), whereas none of the patients with nonrecurrent disease did so. There was no significant correlation between metachronous recurrence after EMR and immunohistochemical staining reactions, including those for PCNA, p53, hMSH2, and hMLH1. None of the patients showed K-ras mutations.Thirty percent of patients with recurrent disease showed MSI-H, whereas none of the patients with nonrecurrent disease did so.
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