| Literature DB >> 24525230 |
Theonie Anastassiadis1, Eric J Brown2.
Abstract
Mutant RAS-driven tumorigenesis was thought for decades to arise independently of wild-type RAS isoforms, but recent evidence indicates wild-type isoforms are involved. In this issue of Cancer Cell, Grabocka and colleagues report how the loss of wild-type RAS alters oncogenic signaling and dampens the DNA-damage response, thereby affecting tumor progression and chemosensitivity.Entities:
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Year: 2014 PMID: 24525230 PMCID: PMC4050974 DOI: 10.1016/j.ccr.2014.01.029
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743