Your browser doesn't support javascript.
loading
Transcription Factor Activities Enhance Markers of Drug Sensitivity in Cancer.
Garcia-Alonso, Luz; Iorio, Francesco; Matchan, Angela; Fonseca, Nuno; Jaaks, Patricia; Peat, Gareth; Pignatelli, Miguel; Falcone, Fiammetta; Benes, Cyril H; Dunham, Ian; Bignell, Graham; McDade, Simon S; Garnett, Mathew J; Saez-Rodriguez, Julio.
Afiliación
  • Garcia-Alonso L; European Molecular Biology Laboratory - European Bioinformatics Institute, Wellcome Genome Campus, Cambridge, United Kingdom.
  • Iorio F; OpenTargets, Wellcome Genome Campus, Cambridge, United Kingdom.
  • Matchan A; European Molecular Biology Laboratory - European Bioinformatics Institute, Wellcome Genome Campus, Cambridge, United Kingdom.
  • Fonseca N; OpenTargets, Wellcome Genome Campus, Cambridge, United Kingdom.
  • Jaaks P; OpenTargets, Wellcome Genome Campus, Cambridge, United Kingdom.
  • Peat G; Wellcome Trust Sanger Institute, Wellcome Genome Campus, Cambridge, United Kingdom.
  • Pignatelli M; European Molecular Biology Laboratory - European Bioinformatics Institute, Wellcome Genome Campus, Cambridge, United Kingdom.
  • Falcone F; Wellcome Trust Sanger Institute, Wellcome Genome Campus, Cambridge, United Kingdom.
  • Benes CH; European Molecular Biology Laboratory - European Bioinformatics Institute, Wellcome Genome Campus, Cambridge, United Kingdom.
  • Dunham I; OpenTargets, Wellcome Genome Campus, Cambridge, United Kingdom.
  • Bignell G; European Molecular Biology Laboratory - European Bioinformatics Institute, Wellcome Genome Campus, Cambridge, United Kingdom.
  • McDade SS; OpenTargets, Wellcome Genome Campus, Cambridge, United Kingdom.
  • Garnett MJ; Centre for Cancer Research and Cell Biology, Queen's University Belfast, Belfast, United Kingdom.
  • Saez-Rodriguez J; Massachusetts General Hospital, Boston, Massachusetts.
Cancer Res ; 78(3): 769-780, 2018 02 01.
Article en En | MEDLINE | ID: mdl-29229604
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.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Farmacogenética / Factores de Transcripción / Biomarcadores de Tumor / Regulación Neoplásica de la Expresión Génica / Bibliotecas de Moléculas Pequeñas / Neoplasias / Antineoplásicos Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Cancer Res Año: 2018 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Farmacogenética / Factores de Transcripción / Biomarcadores de Tumor / Regulación Neoplásica de la Expresión Génica / Bibliotecas de Moléculas Pequeñas / Neoplasias / Antineoplásicos Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Cancer Res Año: 2018 Tipo del documento: Article País de afiliación: Reino Unido Pais de publicación: Estados Unidos