抗药性
癌症治疗
癌症研究
癌症
块(置换群论)
机制(生物学)
免疫系统
抗性(生态学)
药品
联合疗法
靶向治疗
信号转导
调解人
医学
后天抵抗
促炎细胞因子
癌症治疗
药物治疗
肿瘤微环境
生物信息学
免疫疗法
免疫检查点
癌细胞
药理学
下调和上调
阴性治疗反应
免疫学
作用机理
细胞因子
作者
Chan D.K. Nguyen,Chunling Yi
标识
DOI:10.1016/j.trecan.2019.02.010
摘要
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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