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BMC Genomics. 2013;14 Suppl 3:S8. doi: 10.1186/1471-2164-14-S3-S8. Epub 2013 May 28.

Revealing selection in cancer using the predicted functional impact of cancer mutations. Application to nomination of cancer drivers.

Author information

1
Computational Biology Center, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, NY 10065, USA. reva@cbio.mskcc.org.

Abstract

Every malignant tumor has a unique spectrum of genomic alterations including numerous protein mutations. There are also hundreds of personal germline variants to be taken into account. The combinatorial diversity of potential cancer-driving events limits the applicability of statistical methods to determine tumor-specific "driver" alterations among an overwhelming majority of "passengers". An alternative approach to determining driver mutations is to assess the functional impact of mutations in a given tumor and predict drivers based on a numerical value of the mutation impact in a particular context of genomic alterations.Recently, we introduced a functional impact score, which assesses the mutation impact by the value of entropic disordering of the evolutionary conservation patterns in proteins. The functional impact score separates disease-associated variants from benign polymorphisms with an accuracy of ~80%. Can the score be used to identify functionally important non-recurrent cancer-driver mutations? Assuming that cancer-drivers are positively selected in tumor evolution, we investigated how the functional impact score correlates with key features of natural selection in cancer, such as the non-uniformity of distribution of mutations, the frequency of affected tumor suppressors and oncogenes, the frequency of concurrent alterations in regions of heterozygous deletions and copy gain; as a control, we used presumably non-selected silent mutations. Using mutations of six cancers studied in TCGA projects, we found that predicted high-scoring functional mutations as well as truncating mutations tend to be evolutionarily selected as compared to low-scoring and silent mutations. This result justifies prediction of mutations-drivers using a shorter list of predicted high-scoring functional mutations, rather than the "long tail" of all mutations.

PMID:
23819556
PMCID:
PMC3665576
DOI:
10.1186/1471-2164-14-S3-S8
[Indexed for MEDLINE]
Free PMC Article

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