| Literature DB >> 21764851 |
Alison L Dooley1, Monte M Winslow, Derek Y Chiang, Shantanu Banerji, Nicolas Stransky, Talya L Dayton, Eric L Snyder, Stephanie Senna, Charles A Whittaker, Roderick T Bronson, Denise Crowley, Jordi Barretina, Levi Garraway, Matthew Meyerson, Tyler Jacks.
Abstract
Small cell lung cancer (SCLC) is an aggressive cancer often diagnosed after it has metastasized. Despite the need to better understand this disease, SCLC remains poorly characterized at the molecular and genomic levels. Using a genetically engineered mouse model of SCLC driven by conditional deletion of Trp53 and Rb1 in the lung, we identified several frequent, high-magnitude focal DNA copy number alterations in SCLC. We uncovered amplification of a novel, oncogenic transcription factor, Nuclear factor I/B (Nfib), in the mouse SCLC model and in human SCLC. Functional studies indicate that NFIB regulates cell viability and proliferation during transformation.Entities:
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Year: 2011 PMID: 21764851 PMCID: PMC3143937 DOI: 10.1101/gad.2046711
Source DB: PubMed Journal: Genes Dev ISSN: 0890-9369 Impact factor: 11.361