Maity Subhajit, Gridnev Artem, Misra Jyoti R
Department of Biological Sciences, University of Texas at Dallas, Richardson, TX 75080, USA.
Cancers (Basel). 2022 Feb 17;14(4):1029. doi: 10.3390/cancers14041029.
YAP/TAZ are transcriptional coactivators that function as the key downstream effectors of Hippo signaling. They are commonly misregulated in most human cancers, which exhibit a higher level of expression and nuclear localization of YAP/TAZ, and display addiction to YAP-dependent transcription. In the nucleus, these coactivators associate with TEA domain transcription factors (TEAD1-4) to regulate the expression of genes that promote cell proliferation and inhibit cell death. Together, this results in an excessive growth of the cancerous tissue. Further, YAP/TAZ play a critical role in tumor metastasis and chemotherapy resistance by promoting cancer stem cell fate. Furthermore, they affect tumor immunity by promoting the expression of PD-L1. Thus, YAP plays an important role in multiple aspects of cancer biology and thus, provides a critical target for cancer therapy. Here we discuss various assays that are used for conducting high-throughput screens of small molecule libraries for hit identification, and subsequent hit validation for successful discovery of potent inhibitors of YAP-transcriptional activity. Furthermore, we describe the advantages and limitations of these assays.
YAP/TAZ是转录共激活因子,作为Hippo信号通路的关键下游效应器发挥作用。它们在大多数人类癌症中通常存在调控异常,在这些癌症中YAP/TAZ表现出更高水平的表达和核定位,并对YAP依赖的转录呈现成瘾性。在细胞核中,这些共激活因子与TEA结构域转录因子(TEAD1 - 4)结合,以调节促进细胞增殖和抑制细胞死亡的基因的表达。这共同导致癌组织过度生长。此外,YAP/TAZ通过促进癌症干细胞命运在肿瘤转移和化疗耐药中起关键作用。此外,它们通过促进PD - L1的表达影响肿瘤免疫。因此,YAP在癌症生物学的多个方面发挥重要作用,从而为癌症治疗提供了关键靶点。在此我们讨论用于对小分子文库进行高通量筛选以鉴定命中化合物,以及随后对命中化合物进行验证以成功发现YAP转录活性强效抑制剂的各种测定方法。此外,我们描述了这些测定方法的优点和局限性。