异常dnmt3b在肿瘤进展中的作用

Rabia Hameed, Stacey L Raimondi
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引用次数: 2

摘要

癌症是美国最常见的死亡原因之一,仅次于心脏病,是由癌基因和/或肿瘤抑制基因解除管制导致细胞周期控制丧失而引发的。表观遗传变化,如DNA甲基化或组蛋白修饰,在癌细胞中很常见,导致基因调控改变和肿瘤进展。近年来,研究已经在癌细胞中发现了异常的DNA甲基转移酶(DNMT)转录物,而在正常细胞中却没有发现。具体来说,DNMT3B的异常转录本已被证明在肿瘤进展中起作用,包括ΔDNMT3B变异和DNMT3B7。本文就肿瘤中DNMT3B异常引起的表观遗传变化及其在肿瘤进展或抑制中的作用进行综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The role of aberrant DNMT3Bs in tumor progression
Cancer is among the most common causes of death in the United States, second only to heart disease, and is initiated by a loss of cell cycle control resulting from the deregulation of oncogenes and/or tumor suppressor genes. Epigenetic changes, such as DNA methylation or histone modifications, are common in cancer cells leading to altered gene regulation and tumor progression. Recently, studies have identified aberrant DNA methyltransferase ( DNMT ) transcripts in cancer cells but not normal cells. Specifically, aberrant transcripts of DNMT3B have been shown to have a role in tumor progression including the ΔDNMT3B variants as well as DNMT3B7 . This review focuses on epigenetic changes caused by aberrant DNMT3B s in cancer and their role in tumor progression or suppression.
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