Meng Ran, Qin Qiong, Xiong Ying, Wang Yan, Zheng Junfang, Zhao Yuan, Tao Tao, Wang Qiqi, Liu Hua, Wang Songlin, Jiang Wen G, He Junqi
Department of Biochemistry and Molecular Biology, Capital Medical University, Beijing, China.
Beijing Key Laboratory for Tumor Invasion and Metastasis, Beijing International Cooperation Base for Science and Technology on China-UK Cancer Research, Beijing, China.
Oncotarget. 2016 Aug 23;7(34):54983-54997. doi: 10.18632/oncotarget.10713.
G protein-coupled estrogen receptor (GPER) plays an important role in mediating the effects of estradiol. High levels of GPER have been implicated to associate with the malignant progress of invasive breast cancer (IBC). However, the mechanisms by which GPER protein levels were regulated remain unclear. In this study, PDZ protein Na+/H+ exchanger regulatory factor (NHERF1) was found to interact with GPER in breast cancer cells. This interaction was mediated by the PDZ2 domain of NHERF1 and the carboxyl terminal PDZ binding motif of GPER. NHERF1 was demonstrated to facilitate GPER expression at post-transcriptional level and improve GPER protein stability by inhibiting the receptor degradation via ubiquitin-proteasome pathway in a GPER/NHERF1 interaction-dependent manner. In addition, GPER protein levels are positively associated with NHERF1 protein levels in a panel of estrogen receptor (ER)-positive breast cancer cells. Furthermore, analysis of clinical IBC data from The Cancer Genome Atlas (TCGA) showed no significant difference in GPER mRNA levels between ER-positive IBC and normal breast tissues. However, gene set enrichment analysis (GSEA) showed that GPER signaling is ultra-activated in ER-positive IBC when compared with normal and its activation is positively associated with NHERF1 mRNA levels. Taken together, our findings identify NHERF1 as a new binding partner for GPER and its overexpression promotes protein stability and activation of GPER in ER-positive IBC. Our data indicate that regulation of GPER stability by NHERF1 may contribute to GPER-mediated carcinogenesis in ER-positive IBC.
G蛋白偶联雌激素受体(GPER)在介导雌二醇的作用中发挥重要作用。高水平的GPER被认为与浸润性乳腺癌(IBC)的恶性进展相关。然而,GPER蛋白水平受调控的机制仍不清楚。在本研究中,发现PDZ蛋白钠/氢交换调节因子(NHERF1)在乳腺癌细胞中与GPER相互作用。这种相互作用由NHERF1的PDZ2结构域和GPER的羧基末端PDZ结合基序介导。结果表明,NHERF1通过以GPER/NHERF1相互作用依赖的方式抑制泛素-蛋白酶体途径介导的受体降解,在转录后水平促进GPER表达并提高GPER蛋白稳定性。此外,在一组雌激素受体(ER)阳性乳腺癌细胞中,GPER蛋白水平与NHERF1蛋白水平呈正相关。此外,对来自癌症基因组图谱(TCGA)的临床IBC数据的分析显示,ER阳性IBC与正常乳腺组织之间的GPER mRNA水平无显著差异。然而,基因集富集分析(GSEA)表明,与正常组织相比,ER阳性IBC中GPER信号超激活,且其激活与NHERF1 mRNA水平呈正相关。综上所述,我们的研究结果确定NHERF1是GPER的新结合伴侣,其过表达促进ER阳性IBC中GPER的蛋白稳定性和激活。我们的数据表明,NHERF1对GPER稳定性的调节可能有助于ER阳性IBC中GPER介导的致癌作用。