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YAP/TAZ Signaling and Resistance to Cancer Therapy

期刊

TRENDS IN CANCER
卷 5, 期 5, 页码 283-296

出版社

CELL PRESS
DOI: 10.1016/j.trecan.2019.02.010

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资金

  1. NIH [R01CA187090]
  2. Cancer Center Support Grant [CA051008]
  3. DF/HCC Kidney Cancer SPORE [CA101942]
  4. V foundation
  5. Toulmin Pilot Award
  6. Sher Grant
  7. Advocure foundation

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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.

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