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Microsatellite-unstable mucinous colorectal carcinoma occurring in the elderly: comparison with medullary type poorly differentiated adenocarcinoma.

机译:老年人发生微卫星不稳定粘液性大肠癌:与髓样低分化腺癌比较。

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摘要

Mucinous carcinoma and poorly differentiated adenocarcinoma of the large intestine have a high frequency of microsatellite instability, and their occurrence increases gradually with age. To elucidate the clinicopathological and immunohistochemical features of microsatellite-unstable mucinous carcinoma and compare the tumor with medullary type poorly differentiated adenocarcinoma, the clinicopathological status and expression of mucin core and hMLH1 proteins were studied in 15 microsatellite-unstable and 20 microsatellite-stable mucinous colorectal carcinomas occurring in elderly patients, and compared with 23 cases of medullary type poorly differentiated adenocarcinoma in which 21 cases were microsatellite-unstable. Thirteen (87%) of 15 microsatellite-unstable carcinomas exhibited absent hMLH1 expression compared with three (15%) of 20 microsatellite-stable carcinomas (P < 0.01). The proportion (87%) of positive MUC5AC expression in microsatellite-unstable mucinous carcinoma was significantly higher than that (45%) in microsatellite-stable mucinous carcinoma (P = 0.01). Compared with microsatellite-stable mucinous carcinoma, microsatellite-unstable mucinous carcinomas were significantly associated with a proximal location, intra- and peritumoral inflammatory cell infiltration, frequent MUC5AC expression, a low incidence of lymph node metastasis and absent hMLH1 protein expression, which is not different to medullary type poorly differentiated adenocarcinoma except for MUC2 expression and age-related occurrence. These results suggest that microsatellite-unstable mucinous carcinoma occurring in the elderly shares clinicopathological and molecular features with medullary type poorly differentiated adenocarcinoma and that microsatellite instability with absent hMLH1 expression plays an important role in the development of these two carcinomas.
机译:大肠粘液癌和低分化腺癌的微卫星不稳定性频率很高,并且其发生率随着年龄的增长而逐渐增加。为了阐明微卫星不稳定黏液癌的临床病理学和免疫组织化学特征,并与髓样低分化腺癌进行比较,研究了15例微卫星不稳定和20例微卫星不稳定粘液性大肠癌的黏蛋白核心和hMLH1蛋白的临床病理状态和表达。与23例延髓型低分化腺癌相比,其中21例微卫星不稳定。 15例微卫星不稳定癌中有13例(87%)缺乏hMLH1表达,而20例微卫星不稳定癌中有3例(15%)表现出hMLH1表达(P <0.01)。微卫星不稳定粘液癌中MUC5AC阳性表达的比例(87%)显着高于微卫星稳定粘液癌中(45%)(P = 0.01)。与微卫星稳定的粘液性癌相比,微卫星不稳定的粘液性癌与近端位置,肿瘤内和肿瘤周围炎性细胞浸润,MUC5AC频繁表达,淋巴结转移发生率低和缺少hMLH1蛋白表达显着相关。除MUC2表达和与年龄有关的发生外,其余均为髓样低分化腺癌。这些结果表明,老年人中发生的微卫星不稳定粘液性癌与髓样低分化腺癌具有共同的临床病理和分子特征,并且缺乏hMLH1表达的微卫星不稳定性在这两种癌的发展中起着重要作用。

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