| Literature DB >> 27728979 |
Steven K Montalvo1, Lianbo Li2, Kenneth D Westover2.
Abstract
RAS mutations are among the most common genetic alterations found in cancerous tumors but rational criteria or strategies for targeting RAS-dependent tumors are only recently emerging. Clinical and laboratory data suggest that patient selection based on specific RAS mutations will be an essential component of these strategies. A thorough understanding of the biochemical and structural properties of mutant RAS proteins form the theoretical basis for these approaches. Direct inhibition of KRAS G12C by covalent inhibitors is a notable recent example of the RAS mutation-tailored approach that establishes a paradigm for other RAS mutation-centered strategies.Entities:
Keywords: GTPase; RAS; cancer; isoforms
Mesh:
Substances:
Year: 2016 PMID: 27728979 DOI: 10.2217/fon-2016-0363
Source DB: PubMed Journal: Future Oncol ISSN: 1479-6694 Impact factor: 3.404