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巴雷特食管:分子生物学概述

Barrett's esophagus: an overview of the molecular biology.

作者信息

Aldulaimi D, Jankowski J

机构信息

Department of Medicine, University of Birmingham, Edgbaston, UK.

出版信息

Dis Esophagus. 1999;12(3):177-80. doi: 10.1046/j.1442-2050.1999.00043.x.

Abstract

The significance of specialized intestinal metaplasia in the esophagus is its associated risk with esophageal adenocarcinoma. This tumor has increased in incidence by over 70% in 20 years. Specialized intestinal metaplasia is the most important risk factor for adenocarcinoma of the esophagus and has been reported in 9-32% of unselected patients in general endoscopy units. The annual risk of esophageal adenocarcinoma for patients with specialized intestinal metaplasia is thought to be approximately 1%, at least 30 times that of the general population. Those with long segments of specialized intestinal metaplasia are thought to be at the greatest risk. Both environmental and molecular changes have been identified in the transition from squamous epithelium through specialized intestinal metaplasia to esophageal adenocarcinoma. The most important molecular changes include impaired regulation of the cell cycle, altered function of known oncogenes and tumor-suppressor genes, changes in cell adhesion molecules, and aneuploidy. This has given rise to a metaplasia/dysplasia/carcinoma model for the evolution of esophageal carcinoma.

摘要

食管特异性肠化生的意义在于其与食管腺癌相关的风险。这种肿瘤的发病率在20年内增加了70%以上。特异性肠化生是食管腺癌最重要的危险因素,在普通内镜检查单位未经挑选的患者中,其报告发生率为9% - 32%。特异性肠化生患者发生食管腺癌的年风险约为1%,至少是普通人群的30倍。长段特异性肠化生患者被认为风险最大。从鳞状上皮经过特异性肠化生到食管腺癌的转变过程中,已发现环境和分子变化。最重要的分子变化包括细胞周期调控受损、已知癌基因和肿瘤抑制基因功能改变、细胞黏附分子变化以及非整倍体。这就产生了一个食管癌演变的化生/发育异常/癌模型。

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