Pan-cancer transcriptomic analysis associates long non-coding RNAs with key mutational driver events

被引:49
|
作者
Ashouri, Arghavan [1 ]
Sayin, Volkan I. [2 ,3 ]
Van den Eynden, Jimmy [1 ]
Singh, Simranjit X. [2 ,3 ]
Papagiannakopoulos, Thales [2 ,3 ]
Larsson, Erik [1 ]
机构
[1] Univ Gothenburg, Sahlgrenska Acad, Inst Biomed, Dept Med Biochem & Cell Biol, SE-40530 Gothenburg, Sweden
[2] NYU, Sch Med, Dept Pathol, New York, NY 10016 USA
[3] NYU, Sch Med, Perlmutter Canc Ctr, New York, NY 10016 USA
基金
英国医学研究理事会;
关键词
CELL-PROLIFERATION; GENE-EXPRESSION; MESSENGER-RNA; P53; REVEALS; NRF2; LANDSCAPE; INACTIVATION; ANNOTATION; SIGNATURES;
D O I
10.1038/ncomms13197
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Thousands of long non-coding RNAs (lncRNAs) lie interspersed with coding genes across the genome, and a small subset has been implicated as downstream effectors in oncogenic pathways. Here we make use of transcriptome and exome sequencing data from thousands of tumours across 19 cancer types, to identify lncRNAs that are induced or repressed in relation to somatic mutations in key oncogenic driver genes. Our screen confirms known coding and non-coding effectors and also associates many new lncRNAs to relevant pathways. The associations are often highly reproducible across cancer types, and while many lncRNAs are co-expressed with their protein-coding hosts or neighbours, some are intergenic and independent. We highlight lncRNAs with possible functions downstream of the tumour suppressor TP53 and the master antioxidant transcription factor NFE2L2. Our study provides a comprehensive overview of lncRNA transcriptional alterations in relation to key driver mutational events in human cancers.
引用
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页数:13
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