PARADIGM-SHIFT predicts the function of mutations in multiple cancers using pathway impact analysis

被引:75
|
作者
Ng, Sam [1 ,2 ]
Collisson, Eric A. [3 ]
Sokolov, Artem [1 ,2 ]
Goldstein, Theodore [1 ,2 ]
Gonzalez-Perez, Abel [4 ]
Lopez-Bigas, Nuria [5 ,6 ]
Benz, Christopher [7 ]
Haussler, David [1 ,2 ,8 ]
Stuart, Joshua M. [1 ,2 ]
机构
[1] Univ Calif Santa Cruz, Dept Biomol Engn, Santa Cruz, CA 95064 USA
[2] Univ Calif Santa Cruz, CBSE, Santa Cruz, CA 95064 USA
[3] Univ Calif San Francisco, Sch Med, San Francisco, CA 94143 USA
[4] Parc Recerca Biomed Barcelona, E-08003 Barcelona, Spain
[5] Univ Pompeu Fabra, E-08002 Barcelona, Spain
[6] ICREA, E-08010 Barcelona, Spain
[7] Univ Calif Santa Cruz, Buck Inst Aging, Unit Christopher Benz, Canc Therapeut Program Novato 94945, Santa Cruz, CA 95064 USA
[8] Univ Calif Santa Cruz, Howard Hughes Med Inst, Santa Cruz, CA 95064 USA
基金
美国国家科学基金会;
关键词
D O I
10.1093/bioinformatics/bts402
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: A current challenge in understanding cancer processes is to pinpoint which mutations influence the onset and progression of disease. Toward this goal, we describe a method called PARADIGM-SHIFT that can predict whether a mutational event is neutral, gain- or loss-of-function in a tumor sample. The method uses a belief-propagation algorithm to infer gene activity from gene expression and copy number data in the context of a set of pathway interactions. Results: The method was found to be both sensitive and specific on a set of positive and negative controls for multiple cancers for which pathway information was available. Application to the Cancer Genome Atlas glioblastoma, ovarian and lung squamous cancer datasets revealed several novel mutations with predicted high impact including several genes mutated at low frequency suggesting the approach will be complementary to current approaches that rely on the prevalence of events to reach statistical significance.
引用
收藏
页码:I640 / I646
页数:7
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