Literature DB >> 29229604

Transcription Factor Activities Enhance Markers of Drug Sensitivity in Cancer.

Luz Garcia-Alonso1,2, Francesco Iorio1,2, Angela Matchan2,3, Nuno Fonseca1, Patricia Jaaks3, Gareth Peat1,2, Miguel Pignatelli1,2, Fiammetta Falcone4, Cyril H Benes5, Ian Dunham1,2, Graham Bignell2,3, Simon S McDade4, Mathew J Garnett2,3, Julio Saez-Rodriguez6,2,7.   

Abstract

Transcriptional dysregulation induced by aberrant transcription factors (TF) is a key feature of cancer, but its global influence on drug sensitivity has not been examined. Here, we infer the transcriptional activity of 127 TFs through analysis of RNA-seq gene expression data newly generated for 448 cancer cell lines, combined with publicly available datasets to survey a total of 1,056 cancer cell lines and 9,250 primary tumors. Predicted TF activities are supported by their agreement with independent shRNA essentiality profiles and homozygous gene deletions, and recapitulate mutant-specific mechanisms of transcriptional dysregulation in cancer. By analyzing cell line responses to 265 compounds, we uncovered numerous TFs whose activity interacts with anticancer drugs. Importantly, combining existing pharmacogenomic markers with TF activities often improves the stratification of cell lines in response to drug treatment. Our results, which can be queried freely at dorothea.opentargets.io, offer a broad foundation for discovering opportunities to refine personalized cancer therapies.Significance: Systematic analysis of transcriptional dysregulation in cancer cell lines and patient tumor specimens offers a publicly searchable foundation to discover new opportunities to refine personalized cancer therapies. Cancer Res; 78(3); 769-80. ©2017 AACR. ©2017 American Association for Cancer Research.

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Year:  2017        PMID: 29229604      PMCID: PMC6522379          DOI: 10.1158/0008-5472.CAN-17-1679

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


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