| Literature DB >> 32532746 |
Gonzalo Recondo1, Jianwei Che2,3, Pasi A Jänne4,5, Mark M Awad4.
Abstract
Aberrant MET signaling can drive tumorigenesis in several cancer types through a variety of molecular mechanisms including MET gene amplification, mutation, rearrangement, and overexpression. Improvements in biomarker discovery and testing have more recently enabled the selection of patients with MET-dependent cancers for treatment with potent, specific, and novel MET-targeting therapies. We review the known oncologic processes that activate MET, discuss therapeutic strategies for MET-dependent malignancies, and highlight emerging challenges in acquired drug resistance in these cancers. SIGNIFICANCE: Increasing evidence supports the use of MET-targeting therapies in biomarker-selected cancers that harbor molecular alterations in MET. Diverse mechanisms of resistance to MET inhibitors will require the development of novel strategies to delay and overcome drug resistance. ©2020 American Association for Cancer Research.Entities:
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Year: 2020 PMID: 32532746 PMCID: PMC7781009 DOI: 10.1158/2159-8290.CD-19-1446
Source DB: PubMed Journal: Cancer Discov ISSN: 2159-8274 Impact factor: 38.272