| Literature DB >> 28756993 |
Marco Mina1, Franck Raynaud1, Daniele Tavernari1, Elena Battistello2, Stephanie Sungalee3, Sadegh Saghafinia2, Titouan Laessle4, Francisco Sanchez-Vega5, Nikolaus Schultz6, Elisa Oricchio3, Giovanni Ciriello7.
Abstract
Cancer evolves through the emergence and selection of molecular alterations. Cancer genome profiling has revealed that specific events are more or less likely to be co-selected, suggesting that the selection of one event depends on the others. However, the nature of these evolutionary dependencies and their impact remain unclear. Here, we designed SELECT, an algorithmic approach to systematically identify evolutionary dependencies from alteration patterns. By analyzing 6,456 genomes from multiple tumor types, we constructed a map of oncogenic dependencies associated with cellular pathways, transcriptional readouts, and therapeutic response. Finally, modeling of cancer evolution shows that alteration dependencies emerge only under conditional selection. These results provide a framework for the design of strategies to predict cancer progression and therapeutic response.Entities:
Keywords: cancer evolution; conditional selection; interdependent therapeutic response; oncogenic dependencies; selected events
Mesh:
Year: 2017 PMID: 28756993 DOI: 10.1016/j.ccell.2017.06.010
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743