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恶性胸膜间皮瘤:致癌作用、分子遗传学的新进展及未来治疗前景

Malignant pleural mesothelioma: newer aspects of carcinogenesis, molecular genetics, and prospects for future therapies.

作者信息

Donington J S, Mew D J, Pass H I

机构信息

Thoracic Oncology Section, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Surg Oncol. 1995 Aug;4(4):175-85. doi: 10.1016/s0960-7404(10)80034-9.

Abstract

Malignant pleural mesothelioma (MPM) is an asbestos-related disease which, although rare, is having a major social impact, and is, for the majority of cases, an incurable illness. There has been a surge of information regarding data on mesothelial transformation, mesothelioma molecular genetics and somatic gene therapy for this disease. This report summarizes the most recent investigations attempting to characterize the behaviour, on a cellular and molecular level, of MPM, with an emphasis on data from investigations performed at the National Cancer Institute with our collaborators.

摘要

恶性胸膜间皮瘤(MPM)是一种与石棉相关的疾病,尽管罕见,但具有重大社会影响,并且在大多数情况下是一种不治之症。关于间皮细胞转化、间皮瘤分子遗传学以及针对该疾病的体细胞基因治疗的数据信息激增。本报告总结了最近试图在细胞和分子水平上描述MPM行为的研究,重点是美国国立癌症研究所与我们的合作者开展的研究数据。

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