Mao Tsui-Lien, Shih Ie-Ming
Department of Pathology, National Taiwan University College of Medicine, Taipei, Taiwan.
J Gynecol Oncol. 2013 Oct;24(4):376-81. doi: 10.3802/jgo.2013.24.4.376. Epub 2013 Oct 2.
One of the exciting findings in recent cancer genome studies is the discovery of somatic mutations in several chromatin remodeling genes. These studies not only illuminate the emerging roles of chromatin remodeling in the pathogenesis of human cancer but also provide molecular genetic basis of aberrant epigenomic regulation as one of the key mechanisms driving cancer development. This is because chromatin remodeling influences a variety of DNA activities such as replication, transcription, repair, methylation, and recombination. Among the mutated chromatin remodeling genes reported, ARID1A is frequently mutated in a variety of human cancers, especially in endometrium-related neoplasms including ovarian clear cell carcinoma, ovarian endometrioid carcinomas, and uterine endometrioid carcinomas, all of which arise from endometrial epithelium. This review will summarize the recent advances in studying the roles of ARID1A mutations in gynecologic cancers with special emphasis on how this new knowledge will further extend our understanding of the pathogenesis of endometrium-related carcinomas.
近期癌症基因组研究中一项令人兴奋的发现是,在多个染色质重塑基因中发现了体细胞突变。这些研究不仅阐明了染色质重塑在人类癌症发病机制中的新作用,还为异常表观基因组调控作为驱动癌症发展的关键机制之一提供了分子遗传学基础。这是因为染色质重塑会影响多种DNA活动,如复制、转录、修复、甲基化和重组。在已报道的突变染色质重塑基因中,ARID1A在多种人类癌症中频繁发生突变,尤其是在与子宫内膜相关的肿瘤中,包括卵巢透明细胞癌、卵巢子宫内膜样癌和子宫子宫内膜样癌,所有这些癌症均起源于子宫内膜上皮。本综述将总结研究ARID1A突变在妇科癌症中作用的最新进展,特别强调这一新知识将如何进一步扩展我们对子宫内膜相关癌症发病机制的理解。