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YAP1 介导的胰腺星状细胞激活抑制胰腺癌细胞增殖。

YAP1-mediated pancreatic stellate cell activation inhibits pancreatic cancer cell proliferation.

机构信息

Department of Pathology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, PR China; Molecular Pathology Research Center, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, PR China; Department of Pathology, Beijing Tsinghua Changgung Hospital, School of Clinic Medicine, Tsinghua University, Beijing, PR China.

Department of Pathology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, PR China; Molecular Pathology Research Center, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, PR China.

出版信息

Cancer Lett. 2019 Oct 10;462:51-60. doi: 10.1016/j.canlet.2019.07.015. Epub 2019 Jul 25.

Abstract

Pancreatic stellate cells (PSCs) are activated in pancreatic ductal adenocarcinoma (PDAC) and are responsible for dense desmoplastic stroma. Yes-associated protein 1 (YAP1) can induce cancer-associated fibroblast activation in liver and breast tumors, but its effect on PSCs is unknown. In the present study, we determined that YAP1 was highly expressed in the nuclei of PDAC-derived activated PSCs. RNAi-mediated or pharmacological inhibition of YAP1 led to PSC deactivation. In addition, YAP1 stimulated the expression of secreted protein acidic and cysteine rich (SPARC) in PSCs, which was inhibited by RUNX1. SPARC secreted from PSCs inhibited pancreatic cancer cell (PCC) proliferation. High expression of nuclear YAP1 in tumor stroma was significantly correlated with SPARC expression and fibrosis degree in human PDAC tissues. Our study revealed a critical role for YAP1 in the regulation of PSC activation and paracrine signaling. Our findings provide insights into a novel rationale for targeting YAP1 to reprogram the PDAC microenvironment.

摘要

胰腺星状细胞(PSCs)在胰腺导管腺癌(PDAC)中被激活,负责形成致密的纤维性基质。Yes 相关蛋白 1(YAP1)可诱导肝和乳腺肿瘤中的癌相关成纤维细胞激活,但它对 PSCs 的影响尚不清楚。在本研究中,我们发现 YAP1 在源自 PDAC 的激活 PSCs 的核内高度表达。YAP1 的 RNAi 介导或药理学抑制导致 PSC 失活。此外,YAP1 刺激 PSCs 中分泌蛋白酸性和富含半胱氨酸(SPARC)的表达,而 RUNX1 可抑制其表达。PSCs 分泌的 SPARC 抑制胰腺癌细胞(PCC)的增殖。肿瘤基质中核内 YAP1 的高表达与人 PDAC 组织中的 SPARC 表达和纤维化程度显著相关。我们的研究揭示了 YAP1 在调节 PSC 激活和旁分泌信号中的关键作用。我们的研究结果为靶向 YAP1 重塑 PDAC 微环境提供了新的依据。

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