Author:
Dooley Alison L.,Winslow Monte M.,Chiang Derek Y.,Banerji Shantanu,Stransky Nicolas,Dayton Talya L.,Snyder Eric L.,Senna Stephanie,Whittaker Charles A.,Bronson Roderick T.,Crowley Denise,Barretina Jordi,Garraway Levi,Meyerson Matthew,Jacks Tyler
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.
Publisher
Cold Spring Harbor Laboratory
Subject
Developmental Biology,Genetics
Cited by
145 articles.
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