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Bioinformatics. 2013 May 1;29(9):1174-81. doi: 10.1093/bioinformatics/btt131. Epub 2013 Mar 16.

Identification of cancer fusion drivers using network fusion centrality.

Author information

1
Department of Genomic Medicine, UT MD Anderson Cancer Center, Houston, TX 77030, USA. perwu777@gmail.com

Abstract

SUMMARY:

Gene fusions are being discovered at an increasing rate using massively parallel sequencing technologies. Prioritization of cancer fusion drivers for validation cannot be performed using traditional single-gene based methods because fusions involve portions of two partner genes. To address this problem, we propose a novel network analysis method called fusion centrality that is specifically tailored for prioritizing gene fusions. We first propose a domain-based fusion model built on the theory of exon/domain shuffling. The model leads to a hypothesis that a fusion is more likely to be an oncogenic driver if its partner genes act like hubs in a network because the fusion mutation can deregulate normal functions of many other genes and their pathways. The hypothesis is supported by the observation that for most known cancer fusion genes, at least one of the fusion partners appears to be a hub in a network, and even for many fusions both partners appear to be hubs. Based on this model, we construct fusion centrality, a multi-gene-based network metric, and use it to score fusion drivers. We show that the fusion centrality outperforms other single gene-based methods. Specifically, the method successfully predicts most of 38 newly discovered fusions that had validated oncogenic importance. To our best knowledge, this is the first network-based approach for identifying fusion drivers.

AVAILABILITY:

Matlab code implementing the fusion centrality method is available upon request from the corresponding authors.

PMID:
23505294
PMCID:
PMC3634186
DOI:
10.1093/bioinformatics/btt131
[Indexed for MEDLINE]
Free PMC Article

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