| Literature DB >> 26439496 |
Leng Han1, Lixia Diao1, Shuangxing Yu2, Xiaoyan Xu3, Jie Li2, Rui Zhang4, Yang Yang5, Henrica M J Werner6, A Karina Eterovic2, Yuan Yuan1, Jun Li1, Nikitha Nair7, Rosalba Minelli7, Yiu Huen Tsang7, Lydia W T Cheung2, Kang Jin Jeong2, Jason Roszik8, Zhenlin Ju1, Scott E Woodman8, Yiling Lu2, Kenneth L Scott7, Jin Billy Li4, Gordon B Mills9, Han Liang10.
Abstract
Adenosine-to-inosine (A-to-I) RNA editing is a widespread post-transcriptional mechanism, but its genomic landscape and clinical relevance in cancer have not been investigated systematically. We characterized the global A-to-I RNA editing profiles of 6,236 patient samples of 17 cancer types from The Cancer Genome Atlas and revealed a striking diversity of altered RNA-editing patterns in tumors relative to normal tissues. We identified an appreciable number of clinically relevant editing events, many of which are in noncoding regions. We experimentally demonstrated the effects of several cross-tumor nonsynonymous RNA editing events on cell viability and provide the evidence that RNA editing could selectively affect drug sensitivity. These results highlight RNA editing as an exciting theme for investigating cancer mechanisms, biomarkers, and treatments.Entities:
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Year: 2015 PMID: 26439496 PMCID: PMC4605878 DOI: 10.1016/j.ccell.2015.08.013
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743