Analysis of microRNA-target interactions across diverse cancer types

被引:158
|
作者
Jacobsen, Anders [1 ]
Silber, Joachim [2 ,3 ]
Harinath, Girish [2 ,3 ]
Huse, Jason T. [2 ,3 ]
Schultz, Nikolaus [1 ]
Sander, Chris [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Computat Biol Ctr, New York, NY 10021 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Pathol & Human Oncol, New York, NY 10021 USA
[3] Mem Sloan Kettering Canc Ctr, Pathogenesis Program, New York, NY 10021 USA
关键词
THYMINE DNA GLYCOSYLASE; REGULATORY NETWORK; DEMETHYLATION; PATHWAY; TET; 5-METHYLCYTOSINE; IDENTIFICATION; COMPONENTS; PROTEINS; EXCISION;
D O I
10.1038/nsmb.2678
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Little is known about the extent to which individual microRNAs ( miRNAs) regulate common processes of tumor biology across diverse cancer types. Using molecular profiles of >3,000 tumors from 11 human cancer types in The Cancer Genome Atlas, we systematically analyzed expression of miRNAs and mRNAs across cancer types to infer recurrent cancer-associated miRNA-target relationships. As we expected, the inferred relationships were consistent with sequence-based predictions and published data from miRNA perturbation experiments. Notably, miRNAs with recurrent target relationships were frequently regulated by genetic and epigenetic alterations across the studied cancer types. We also identify new examples of miRNAs that coordinately regulate cancer pathways, including the miR-29 family, which recurrently regulates active DNA demethylation pathway members TET1 and TDG. The online resource http://cancerminer.org allows exploration and prioritization of miRNA-target interactions that potentially regulate tumorigenesis.
引用
收藏
页码:1325 / U131
页数:9
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