| Literature DB >> 31174841 |
Chan D K Nguyen1, Chunling Yi2.
Abstract
Drug resistance is a major challenge in cancer treatment. Emerging evidence indicates that deregulation of YAP/TAZ signaling may be a major mechanism of intrinsic and acquired resistance to various targeted and chemotherapies. Moreover, YAP/TAZ-mediated expression of PD-L1 and multiple cytokines is pivotal for tumor immune evasion. While direct inhibitors of YAP/TAZ are still under development, FDA-approved drugs that indirectly block YAP/TAZ activation or critical downstream targets of YAP/TAZ have shown promise in the clinic in reducing therapy resistance. Finally, BET inhibitors, which reportedly block YAP/TAZ-mediated transcription, present another potential venue to overcome YAP/TAZ-induced drug resistance.Entities:
Keywords: Cancer therapy resistance; Hippo pathway; TAZ; YAP
Mesh:
Substances:
Year: 2019 PMID: 31174841 PMCID: PMC6557283 DOI: 10.1016/j.trecan.2019.02.010
Source DB: PubMed Journal: Trends Cancer ISSN: 2405-8025