Jia Qiongqiong, Wang Hailong, Bi Beibei, Han Xiaoyu, Jia Yuanyuan, Zhang Lingling, Fang Lanlan, Thakur Avinash, Cheng Jung-Chien
Center for Reproductive Medicine, Henan Key Laboratory of Reproduction and Genetics, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
The Vancouver Prostate Centre, Department of Urologic Sciences, University of British Columbia, Vancouver, BC, Canada.
Reprod Sci. 2025 Feb;32(2):404-416. doi: 10.1007/s43032-024-01673-x. Epub 2024 Aug 13.
Amphiregulin (AREG) stimulates human epithelial ovarian cancer (EOC) cell invasion by downregulating E-cadherin expression. YAP is a transcriptional cofactor that has been shown to regulate tumorigenesis. This study aimed to examine whether AREG activates YAP in EOC cells and explore the roles of YAP in AREG-induced downregulation of E-cadherin and cell invasion. Analysis of the Cancer Genome Atlas (TCGA) showed that upregulation of AREG and EGFR were associated with poor survival in human EOC. Treatment of SKOV3 human EOC cells with AREG induced the activation of YAP. In addition, AREG downregulated E-cadherin, upregulated Egr-1 and Slug, and stimulated cell invasion. Using gain- and loss-of-function approaches, we showed that YAP was required for the AREG-upregulated Egr-1 and Slug expression. Furthermore, YAP was also involved in AREG-induced downregulation of E-cadherin and cell invasion. This study provides evidence that AREG stimulates human EOC cell invasion by downregulating E-cadherin expression through the YAP/Egr-1/Slug signaling.
双调蛋白(AREG)通过下调E-钙黏蛋白的表达来刺激人上皮性卵巢癌(EOC)细胞的侵袭。YAP是一种转录辅因子,已被证明可调节肿瘤发生。本研究旨在检测AREG是否能激活EOC细胞中的YAP,并探究YAP在AREG诱导的E-钙黏蛋白下调和细胞侵袭中的作用。癌症基因组图谱(TCGA)分析显示,AREG和表皮生长因子受体(EGFR)的上调与人类EOC患者的不良生存相关。用AREG处理SKOV3人EOC细胞可诱导YAP的激活。此外,AREG下调E-钙黏蛋白,上调早期生长反应蛋白-1(Egr-1)和锌指蛋白Slug,并刺激细胞侵袭。采用功能获得和功能缺失方法,我们发现YAP是AREG上调Egr-1和Slug表达所必需的。此外,YAP还参与了AREG诱导的E-钙黏蛋白下调和细胞侵袭。本研究提供了证据,表明AREG通过YAP/Egr-1/Slug信号通路下调E-钙黏蛋白的表达来刺激人EOC细胞的侵袭。