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鉴定脯氨酰异构酶 Pin1 为乳腺癌细胞中 YAP/TAZ 的新型正调控因子。

Identification of Prolyl isomerase Pin1 as a novel positive regulator of YAP/TAZ in breast cancer cells.

机构信息

Department of Pathology and Molecular Medicine, Queen's University, Kingston, Canada.

出版信息

Sci Rep. 2019 Apr 23;9(1):6394. doi: 10.1038/s41598-019-42767-w.

Abstract

The Hippo signalling pathway plays very important roles in tumorigenesis, metastasis, organ size control, and drug resistance. Although, it has been shown that the two major components of Hippo pathway, YAP and TAZ, play very crucial role in tumorigenesis and drug resistance, the exact molecular mechanisms are still unknown. Recently, we have shown that the prolyl isomerase Pin1 regulates the activity of Hippo pathway through interaction with Hippo component LATS kinase. Thus we asked if Pin1 is also able to interact with other Hippo pathway components. Therefore, in order to investigate whether Pin1 can interacts with other components of the Hippo pathway, we performed GST-pull down and co-immunoprecipitation (Co-IP) assays and have identified two Hippo components YAP and TAZ oncoproteins as novel binding partner of Pin1. We found that Pin1 interacts with YAP/TAZ in a phosphorylation-independent manner and WW domain of Pin1 is necessary for this interaction. Moreover, by using real time qRT-PCR, Cycloheximide chase, luciferase reporter, cell viability and soft agar assays, we have shown that Pin1 increases the tumorigenic and drug-resistant activity of YAP/TAZ through stabilization of YAP/TAZ at protein levels. Together, we have identified Pin1 as a novel positive regulator of YAP/TAZ in tumorigenesis and drug resistance of breast cancer cells. These findings will provide a significant contribution for targeting the Pin1-YAP/TAZ signaling for the successful treatment of tumorigenesis and drug resistance of breast and other cancers in the future.

摘要

Hippo 信号通路在肿瘤发生、转移、器官大小控制和耐药性方面发挥着非常重要的作用。尽管已经表明 Hippo 通路的两个主要组成部分 YAP 和 TAZ 在肿瘤发生和耐药性中起着至关重要的作用,但确切的分子机制尚不清楚。最近,我们已经表明,脯氨酰异构酶 Pin1 通过与 Hippo 成分 LATS 激酶相互作用来调节 Hippo 通路的活性。因此,我们想知道 Pin1 是否也能够与 Hippo 通路的其他成分相互作用。因此,为了研究 Pin1 是否可以与 Hippo 通路的其他成分相互作用,我们进行了 GST 下拉和共免疫沉淀(Co-IP)实验,鉴定出 YAP 和 TAZ 癌蛋白这两种 Hippo 通路成分是 Pin1 的新结合伴侣。我们发现 Pin1 以磷酸化非依赖性的方式与 YAP/TAZ 相互作用,并且 Pin1 的 WW 结构域对于这种相互作用是必需的。此外,通过实时 qRT-PCR、环己酰亚胺追踪、荧光素酶报告基因、细胞活力和软琼脂测定,我们表明 Pin1 通过稳定 YAP/TAZ 在蛋白质水平上增加 YAP/TAZ 的致瘤和耐药活性。总之,我们已经确定 Pin1 是乳腺癌细胞中 YAP/TAZ 致癌和耐药性的新型正调控因子。这些发现将为针对 Pin1-YAP/TAZ 信号通路以成功治疗乳腺癌和其他癌症的肿瘤发生和耐药性提供重要贡献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5935/6478839/994108732945/41598_2019_42767_Fig1_HTML.jpg

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