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ERβ 介导的 circATP2B1 和 miR-204-3p 信号改变促进透明细胞肾细胞癌的侵袭。

ERβ-Mediated Alteration of circATP2B1 and miR-204-3p Signaling Promotes Invasion of Clear Cell Renal Cell Carcinoma.

机构信息

Department of Urology, the Second Hospital of Hebei Medical University, Shijiazhuang, China.

George Whipple Lab for Cancer Research, Departments of Urology, Pathology, Radiation Oncology, and The Wilmot Cancer Center, University of Rochester Medical Center, Rochester, New York.

出版信息

Cancer Res. 2018 May 15;78(10):2550-2563. doi: 10.1158/0008-5472.CAN-17-1575. Epub 2018 Feb 28.

DOI:10.1158/0008-5472.CAN-17-1575
PMID:29490945
Abstract

Early studies have indicated that estrogen receptor beta (ERβ) can influence the progression of clear cell renal cell carcinoma (ccRCC). Here, we report the mechanistic details of ERβ-mediated progression of ccRCC. ERβ increased ccRCC cell invasion via suppression of circular RNA ATP2B1 (circATP2B1) expression by binding directly to the 5' promoter region of its host gene ATPase plasma membrane Ca2 transporting 1 (ATP2B1). ERβ-suppressed circATP2B1 then led to reduced miR-204-3p, which increased fibronectin 1 (FN1) expression and enhanced ccRCC cell invasion. Targeting ERβ with shRNA suppressed ccRCC metastasis in a murine model of RCC; adding circATP2B1 shRNA partly reversed this effect. Consistent with these experimental results, ccRCC patient survival data from The Cancer Genome Atlas indicated that a patient with higher ERβ and FN1 expression had worse overall survival and a patient with higher miR-204-3p expression had significantly better overall survival. Together, these results suggest that ERβ promotes ccRCC cell invasion by altering the ERβ/circATP2B1/miR-204-3p/FN1 axis and that therapeutic targeting of this newly identified pathway may better prevent ccRCC progression. These results identify an ERβ/circATP2B1/miR-204-3p/FN1 signaling axis in RCC, suggesting ERβ and circular RNA ATP2B1 as prognostic biomarkers for this disease. .

摘要

早期研究表明,雌激素受体β(ERβ)可以影响透明细胞肾细胞癌(ccRCC)的进展。在这里,我们报告了 ERβ 介导的 ccRCC 进展的机制细节。ERβ 通过直接结合其宿主基因 ATP 酶质膜 Ca2+转运 1(ATP2B1)的 5'启动子区域,抑制环状 RNA ATP2B1(circATP2B1)的表达,从而增加 ccRCC 细胞的侵袭。受 ERβ 抑制的 circATP2B1 随后导致 miR-204-3p 减少,从而增加纤连蛋白 1(FN1)的表达并增强 ccRCC 细胞的侵袭。用 shRNA 靶向 ERβ 在 RCC 的小鼠模型中抑制了 ccRCC 的转移;添加 circATP2B1 shRNA 部分逆转了这种作用。与这些实验结果一致,从癌症基因组图谱中获得的 ccRCC 患者生存数据表明,ERβ 和 FN1 表达较高的患者总生存率较差,miR-204-3p 表达较高的患者总生存率显著提高。总之,这些结果表明,ERβ 通过改变 ERβ/circATP2B1/miR-204-3p/FN1 轴促进 ccRCC 细胞侵袭,并且针对该新鉴定的途径的治疗靶向可能更好地预防 ccRCC 的进展。这些结果确定了 RCC 中的 ERβ/circATP2B1/miR-204-3p/FN1 信号轴,表明 ERβ 和环状 RNA ATP2B1 可作为该疾病的预后生物标志物。

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