Warren Janine S A, Xiao Yuxuan, Lamar John M
Department of Molecular and Cellular Physiology, Albany Medical College, Albany, NY 12208, USA.
Cancers (Basel). 2018 Apr 10;10(4):115. doi: 10.3390/cancers10040115.
Yes-Associated Protein (YAP) and Transcriptional Co-activator with PDZ-binding Motif (TAZ) have both emerged as important drivers of cancer progression and metastasis. YAP and TAZ are often upregulated or nuclear localized in aggressive human cancers. There is abundant experimental evidence demonstrating that YAP or TAZ activation promotes cancer formation, tumor progression, and metastasis. In this review we summarize the evidence linking YAP/TAZ activation to metastasis, and discuss the roles of YAP and TAZ during each step of the metastatic cascade. Collectively, this evidence strongly suggests that inappropriate YAP or TAZ activity plays a causal role in cancer, and that targeting aberrant YAP/TAZ activation is a promising strategy for the treatment of metastatic disease. To this end, we also discuss several potential strategies for inhibiting YAP/TAZ activation in cancer and the challenges each strategy poses.
Yes相关蛋白(YAP)和含PDZ结合基序的转录共激活因子(TAZ)已成为癌症进展和转移的重要驱动因素。YAP和TAZ在侵袭性人类癌症中常上调或定位于细胞核。有大量实验证据表明,YAP或TAZ激活促进癌症形成、肿瘤进展和转移。在本综述中,我们总结了将YAP/TAZ激活与转移联系起来的证据,并讨论了YAP和TAZ在转移级联反应每个步骤中的作用。总体而言,这些证据有力地表明,YAP或TAZ的异常活性在癌症中起因果作用,靶向异常的YAP/TAZ激活是治疗转移性疾病的一种有前景的策略。为此,我们还讨论了几种抑制癌症中YAP/TAZ激活的潜在策略以及每种策略带来的挑战。