| Literature DB >> 30686761 |
Amit J Sabnis1, Trever G Bivona2.
Abstract
Identification of the genomic drivers of cancer has led to the clinical development of targeted therapies that strike at the heart of many malignancies. Nonetheless, many cancers outsmart such precision-medicine efforts, and thus therapeutic resistance contributes significantly to cancer mortality. Attempts to understand the basis for resistance in patient samples and laboratory models has yielded two major benefits: one, more effective chemical inhibitors and rational combination therapies are now employed to prevent or circumvent resistance pathways; and two, our understanding of how oncogenic mutations drive cancer cell survival and oncogene addiction is deeper and broader, highlighting downstream or parallel cellular programs that shape these phenotypes. This review discusses emerging principles of resistance to therapies targeted against key oncogenic drivers.Entities:
Keywords: cancer; oncogene addiction; resistance; tyrosine kinase inhibitors
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Year: 2019 PMID: 30686761 PMCID: PMC6401263 DOI: 10.1016/j.molmed.2018.12.009
Source DB: PubMed Journal: Trends Mol Med ISSN: 1471-4914 Impact factor: 11.951