State Key Laboratory of Brain and Cognitive Sciences, Institute of Biophysics, Chinese Academy of Sciences, Beijing, China.
Cancer Res. 2013 Jun 15;73(12):3615-24. doi: 10.1158/0008-5472.CAN-12-3793. Epub 2013 Apr 10.
Transcription coactivator Yes-associated protein (YAP) plays an important role in the regulation of cell proliferation and apoptosis. Here, we identify a new role of YAP in the regulation of cellular senescence. We find that the expression levels of YAP proteins decrease following the replication-induced cellular senescence in IMR90 cells. Silencing of YAP inhibits cell proliferation and induces premature senescence. In additional experiments, we observe that cellular senescence induced by YAP deficiency is TEAD- and Rb/p16/p53-dependent. Furthermore, we show that Cdk6 is a direct downstream target gene of YAP in the regulation of cellular senescence, and the expression of Cdk6 is through the YAP-TEAD complex. Ectopic expression of Cdk6 rescued YAP knockdown-induced senescence. Finally, we find that downregulation of YAP in tumor cells increases senescence in response to chemotherapeutic agents, and YAP or Cdk6 expression rescues cellular senescence. Taken together, our findings define the critical role of YAP in the regulation of cellular senescence and provide a novel insight into a potential chemotherapeutic avenue for tumor suppression.
转录共激活因子 Yes 相关蛋白 (YAP) 在细胞增殖和凋亡的调控中发挥着重要作用。在这里,我们发现了 YAP 在细胞衰老调控中的一个新作用。我们发现,在 IMR90 细胞中,复制诱导的细胞衰老后 YAP 蛋白的表达水平降低。沉默 YAP 可抑制细胞增殖并诱导过早衰老。在额外的实验中,我们观察到 YAP 缺失诱导的细胞衰老依赖于 TEAD 和 Rb/p16/p53。此外,我们表明 Cdk6 是 YAP 在细胞衰老调控中的一个直接下游靶基因,Cdk6 的表达是通过 YAP-TEAD 复合物实现的。Cdk6 的异位表达挽救了 YAP 敲低诱导的衰老。最后,我们发现肿瘤细胞中 YAP 的下调增加了对化疗药物的衰老反应,而 YAP 或 Cdk6 的表达挽救了细胞衰老。总之,我们的研究结果定义了 YAP 在细胞衰老调控中的关键作用,并为肿瘤抑制的潜在化疗途径提供了新的见解。