Department of Hepatopancreatobiliary Surgery, The Affiliated Wuxi No. 2 People's Hospital of Nanjing Medical University, Wuxi, China.
Jiangsu Provincial Key Laboratory on Parasite and Vector Control Technology, Jiangsu Institute of Parasitic Diseases, Wuxi, China.
Cancer Sci. 2020 May;111(5):1514-1527. doi: 10.1111/cas.14344. Epub 2020 Feb 29.
Estrogen-related receptor-α (ERRα) is a nuclear receptor of transcription factor that binds to estrogen responsive elements and estrogen-related responsive elements. Estrogen-related receptor-α is involved in metabolic processes and implicated in the progression and growth of several human malignancies. However, the biologic role and clinical significance of ERRα in gallbladder cancer (GBC) remains to be clarified. Here, we reported that ERRα protein expression was notably higher in GBC tissues than in cholecystitis tissues, and that the aberrantly higher ERRα expression was positively correlated with advanced TNM stage and indicated dismal prognosis of GBC (P < .01). In GBC cell lines NOZ and OCUG, the targeted depletion of ERRα retarded the growth and suppressed the migration and invasive capabilities of GBC cells, and inhibited epithelial-mesenchymal transition by decreasing the expression of mesenchymal markers and elevating the expression of epithelial markers. Moreover, ERRα knockdown inhibited tumor growth in nude mice and led to decreased expression levels of Nectin-4, p-PI3K p85α, and p-AKT. Overexpression of ERRα in the GBC-SD cell line showed exactly the opposite effect. The targeted inhibition of Nectin-4 antagonized GBC cell proliferation and invasion, which were induced by ERRα upregulation. Moreover, Nectin-4 depletion inhibited the ERRα-induced activation of the PI3K/AKT pathway. Chromatin immunoprecipitation analysis and dual-luciferase reporter gene assays showed that ERRα enhanced the transcription of Nectin-4 by binding to the promoter of Nectin-4. In conclusion, our data indicated that ERRα could be a potential target for the genetic treatment of GBC.
雌激素相关受体-α(ERRα)是一种核转录因子受体,它与雌激素反应元件和雌激素相关反应元件结合。ERRα 参与代谢过程,并与几种人类恶性肿瘤的进展和生长有关。然而,ERRα 在胆囊癌(GBC)中的生物学作用和临床意义仍有待阐明。在这里,我们报道 ERRα 蛋白表达在 GBC 组织中明显高于胆囊炎组织,并且异常高的 ERRα 表达与晚期 TNM 分期呈正相关,并预示 GBC 的预后不良(P<.01)。在 GBC 细胞系 NOZ 和 OCUG 中,靶向敲低 ERRα 可抑制 GBC 细胞的生长和迁移侵袭能力,并通过降低间充质标志物的表达和升高上皮标志物的表达来抑制上皮-间充质转化。此外,ERRα 敲低抑制裸鼠肿瘤生长,并导致 Nectin-4、p-PI3K p85α 和 p-AKT 的表达水平降低。在 GBC-SD 细胞系中过表达 ERRα 则表现出完全相反的效果。靶向敲低 Nectin-4 拮抗 ERRα 上调诱导的 GBC 细胞增殖和侵袭。此外,Nectin-4 耗竭抑制了 ERRα 诱导的 PI3K/AKT 通路的激活。染色质免疫沉淀分析和双荧光素酶报告基因检测表明,ERRα 通过结合 Nectin-4 启动子增强 Nectin-4 的转录。总之,我们的数据表明 ERRα 可能是 GBC 基因治疗的潜在靶点。