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Hypermethylation of the hMLH1 promoter with absent hMLH1 expression in medullary-type poorly differentiated colorectal adenocarcinoma in the elderly

机译:老年人延髓型低分化大肠腺癌中hMLH1表达缺失的hMLH1启动子的超甲基化

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To clarify the significance of hMLH1 promoter hypermethylation in the development of medullary-type poorly differentiated colorectal adenocarcinoma, we studied the status of promoter methylation and hMLH1 expression in 23 medullary-type and 12 pleomorphic-type carcinomas, as well as the pathology and microsatellite status. In medullary-type carcinomas, the percentages of cases with promoter methylation (83%) and an absence of hMLH1 expression (91%) were significantly higher than in pleomorphic-type carcinomas (14 and 17%), respectively. The rate of microsatellite instability in the medullary type was significantly higher than that of the pleomorphic type (87 vs 40%, PhMLH1 promoter methylation, absent expression of hMLH1 protein, microsatellite instability, as well as a proximal location, a Crohn's-like lymphoid reaction, a low incidence of lymph node metastasis, and a favorable outcome. Medullary-type carcinomas accumulated with advancing age, especially in the female. These results indicated that hMLH1 hypermethylation, concurrent with a lack of its protein expression, may play an important role in the development of medullary-type poorly differentiated colorectal adenocarcinomas in the elderly.
机译:为了阐明hMLH1启动子高甲基化在延髓型低分化结直肠腺癌发展中的重要性,我们研究了23种髓样型和12种多形性癌中启动子甲基化和hMLH1表达的状态,以及病理学和微卫星状态。在髓样癌中,启动子甲基化的病例(83%)和没有hMLH1表达的病例(91%)的百分比分别明显高于多形性癌(14%和17%)。延髓型微卫星的不稳定性率明显高于多形型(87 vs 40 %,PhMLH1启动子甲基化,hMLH1蛋白缺乏表达,微卫星不稳定性,以及近端位置,克罗恩氏样淋巴样反应,淋巴结转移的发生率低,预后良好;随着年龄的增长,髓样癌的发生越来越多,尤其是女性;这些结果表明,hMLH1甲基化过高并缺乏其蛋白表达,可能起重要作用。老年人延髓型低分化大肠腺癌的发展

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