A novel independence test for somatic alterations in cancer shows that biology drives mutual exclusivity but chance explains most co-occurrence

被引:100
作者
Canisius, Sander [1 ]
Martens, John W. M. [2 ]
Wessels, Lodewyk F. A. [1 ,3 ,4 ]
机构
[1] Netherlands Canc Inst, Dept Mol Carcinogenesis, Plesmanlaan 121, NL-1066 CX Amsterdam, Netherlands
[2] Erasmus Univ, Med Ctr, Dept Med Oncol, Rotterdam, Netherlands
[3] Delft Univ Technol, Fac EEMCS, Delft, Netherlands
[4] Canc Genom Netherlands, Amsterdam, Netherlands
关键词
Mutual exclusivity; Co-occurrence; Computational biology; TUMOR-SUPPRESSOR; CELL-CYCLE; MUTATIONS; GENE; ACTIVATION; MODEL; IDENTIFICATION; LANDSCAPES; DISCOVERY; APOPTOSIS;
D O I
10.1186/s13059-016-1114-x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
In cancer, mutually exclusive or co-occurring somatic alterations across genes can suggest functional interactions. Existing tests for such patterns make the unrealistic assumption of identical gene alteration probabilities across tumors. We present Discrete Independence Statistic Controlling for Observations with Varying Event Rates (DISCOVER), a novel test that is more sensitive than other methods and controls its false positive rate. A pan-cancer analysis using DISCOVER finds no evidence for widespread co-occurrence, and most co-occurrences previously detected do not exceed expectation by chance. Many mutual exclusivities are identified involving well-known genes related to cell cycle and growth factor signaling, as well as lesser known regulators of Hedgehog signaling.
引用
收藏
页数:17
相关论文
共 47 条
[1]  
[Anonymous], 2009, MSRTR200953
[2]   Genetic Interactions in Cancer Progression and Treatment [J].
Ashworth, Alan ;
Lord, Christopher J. ;
Reis-Filho, Jorge S. .
CELL, 2011, 145 (01) :30-38
[3]   Systematic identification of cancer driving signaling pathways based on mutual exclusivity of genomic alterations [J].
Babur, Ozgun ;
Gonen, Mithat ;
Aksoy, Bulent Arman ;
Schultz, Nikolaus ;
Ciriello, Giovanni ;
Sander, Chris ;
Demir, Emek .
GENOME BIOLOGY, 2015, 16
[4]   Overlapping correlation clustering [J].
Bonchi, Francesco ;
Gionis, Aristides ;
Ukkonen, Antti .
KNOWLEDGE AND INFORMATION SYSTEMS, 2013, 35 (01) :1-32
[5]   A Network Model of a Cooperative Genetic Landscape in Brain Tumors [J].
Bredel, Markus ;
Scholtens, Denise M. ;
Harsh, Griffith R. ;
Bredel, Claudia ;
Chandler, James P. ;
Renfrow, Jaclyn J. ;
Yadav, Ajay K. ;
Vogel, Hannes ;
Scheck, Adrienne C. ;
Tibshirani, Robert ;
Sikic, Branimir I. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2009, 302 (03) :261-275
[6]   Modularity-based graph partitioning using conditional expected models [J].
Chang, Yu-Teng ;
Leahy, Richard M. ;
Pantazis, Dimitrios .
PHYSICAL REVIEW E, 2012, 85 (01)
[7]   Mutual exclusivity analysis identifies oncogenic network modules [J].
Ciriello, Giovanni ;
Cerami, Ethan ;
Sander, Chris ;
Schultz, Nikolaus .
GENOME RESEARCH, 2012, 22 (02) :398-406
[8]   TiMEx: a waiting time model for mutually exclusive cancer alterations [J].
Constantinescu, Simona ;
Szczurek, Ewa ;
Mohammadi, Pejman ;
Rahnenfuehrer, Joerg ;
Beerenwinkel, Niko .
BIOINFORMATICS, 2016, 32 (07) :968-975
[9]   Pan-cancer genetic analysis identifies PARK2 as a master regulator of G1/S cyclins [J].
Gong, Yongxing ;
Zack, Travis Ian ;
Morris, Luc G. T. ;
Lin, Kan ;
Hukkelhoven, Ellen ;
Raheja, Radhika ;
Tan, I-Li ;
Turcan, Sevin ;
Veeriah, Selvaraju ;
Meng, Shasha ;
Viale, Agnes ;
Schumacher, Steven E. ;
Palmedo, Perry ;
Beroukhim, Rameen ;
Chan, Timothy A. .
NATURE GENETICS, 2014, 46 (06) :588-594
[10]   Copy Number Analysis Identifies Novel Interactions Between Genomic Loci in Ovarian Cancer [J].
Gorringe, Kylie L. ;
George, Joshy ;
Anglesio, Michael S. ;
Ramakrishna, Manasa ;
Etemadmoghadam, Dariush ;
Cowin, Prue ;
Sridhar, Anita ;
Williams, Louise H. ;
Boyle, Samantha E. ;
Yanaihara, Nozomu ;
Okamoto, Aikou ;
Urashima, Mitsuyoshi ;
Smyth, Gordon K. ;
Campbell, Ian G. ;
Bowtell, David D. L. .
PLOS ONE, 2010, 5 (09) :1-13