RNA编辑
核糖核酸
生物
转录组
阿达尔
胞苷脱氨酶
非编码RNA
遗传学
计算生物学
基因
基因表达
作者
Bora E. Baysal,Shraddha Sharma,Seyedsasan Hashemikhabir,Sarath Chandra Janga
出处
期刊:Cancer Research
[American Association for Cancer Research]
日期:2017-07-13
卷期号:77 (14): 3733-3739
被引量:60
标识
DOI:10.1158/0008-5472.can-17-0520
摘要
Several adenosine or cytidine deaminase enzymes deaminate transcript sequences in a cell type or environment-dependent manner by a programmed process called RNA editing. RNA editing enzymes catalyze A>I or C>U transcript alterations and have the potential to change protein coding sequences. In this brief review, we highlight some recent work that shows aberrant patterns of RNA editing in cancer. Transcriptome sequencing studies reveal increased or decreased global RNA editing levels depending on the tumor type. Altered RNA editing in cancer cells may provide a selective advantage for tumor growth and resistance to apoptosis. RNA editing may promote cancer by dynamically recoding oncogenic genes, regulating oncogenic gene expression by noncoding RNA and miRNA editing, or by transcriptome scale changes in RNA editing levels that may affect innate immune signaling. Although RNA editing markedly increases complexity of the cancer cell transcriptomes, cancer-specific recoding RNA editing events have yet to be discovered. Epitranscriptomic changes by RNA editing in cancer represent a novel mechanism contributing to sequence diversity independently of DNA mutations. Therefore, RNA editing studies should complement genome sequence data to understand the full impact of nucleic acid sequence alterations in cancer. Cancer Res; 77(14); 3733-9. ©2017 AACR.
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