RASSF1 Polymorphisms in Cancer.

Molecular biology international Pub Date : 2012-01-01 Epub Date: 2012-05-31 DOI:10.1155/2012/365213
Marilyn Gordon, Mohamed El-Kalla, Shairaz Baksh
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Abstract

Ras association domain family 1A (RASSF1A) is one of the most epigenetically silenced elements in human cancers. Localized on chromosome 3, it has been demonstrated to be a bone fide tumor suppressor influencing cell cycle events, microtubule stability, apoptosis, and autophagy. Although it is epigenetically silenced by promoter-specific methylation in cancers, several somatic nucleotide changes (polymorphisms) have been identified in RASSF1A in tissues from cancer patients. We speculate that both nucleotide changes and epigenetic silencing result in loss of the RASSF1A tumor suppressor function and the appearance of enhanced growth. This paper will summarize what is known about the origin of these polymorphisms and how they have helped us understand the biological role of RASSF1A.

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癌症中的 RASSF1 多态性。
Ras 关联结构域家族 1A(RASSF1A)是人类癌症中表观遗传沉默最多的基因之一。它位于 3 号染色体上,已被证明是一种真正的肿瘤抑制因子,可影响细胞周期事件、微管稳定性、细胞凋亡和自噬。虽然它在癌症中会因启动子特异性甲基化而被表观遗传学沉默,但在癌症患者的组织中已发现 RASSF1A 存在几种体细胞核苷酸变化(多态性)。我们推测,核苷酸变化和表观遗传沉默都会导致 RASSF1A 肿瘤抑制功能的丧失和生长增强的出现。本文将总结这些多态性的来源以及它们如何帮助我们了解 RASSF1A 的生物学作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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