Circ0001429通过结合miR-205-5p和促进VEGFA表达调控膀胱癌的进展。

IF 1.9
Wenfeng Cao, Youguang Zhao, Liang Wang, Xiaoke Huang
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引用次数: 55

摘要

目的:研究circ0001429、miR-205-5p和血管内皮生长因子(VEGFA)在膀胱癌组织中的表达及其对膀胱癌细胞增殖、迁移和凋亡的影响。方法:应用Arraystar Human CircRNA芯片分析CircRNA在4种膀胱癌组织与配对的邻近正常膀胱组织中的差异表达。采用实时定量PCR检测circ0001429在组织标本中的表达。采用生物信息学、RNA免疫沉淀法和荧光素酶报告基因法验证circ0001429、miR-205-5p和VEGFA在膀胱癌中的关系。CCK8法检测细胞增殖,transwell迁移法验证circ0001429和miR-205-5p在细胞迁移中的作用。流式细胞术和TUNEL染色观察对细胞凋亡能力的影响。异种移植实验也验证了circ0001429对体内肿瘤生长的影响。结果:与配对的邻近正常膀胱组织相比,膀胱癌组织中circ0001429和VEGFA的表达上调,而miR-205-5p的表达下调。Circ0001429增强了T24细胞和5637细胞的体外增殖和转移能力,但减少了细胞凋亡。体内实验揭示了sh-circ0001429在肿瘤生长和肺转移中的抑制作用。Circ0001429海绵靶向VEGFA的miR-205-5p,从而调节VEGFA的蛋白水平。同时,miR-205-5p抑制膀胱癌细胞活力和迁移能力,促进膀胱癌细胞凋亡。Circ0001429可通过miR-205-5p增加VEGFA表达,从而加速细胞增殖、迁移和侵袭性。结论:Circ0001429和VEGFA在膀胱癌中高表达,miR-205-5p在膀胱癌中低表达。circ0001429可靶向miR-205-5p调控VEGFA,促进膀胱癌的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Circ0001429 regulates progression of bladder cancer through binding miR-205-5p and promoting VEGFA expression.

Objective: This study investigates expressions of circ0001429, miR-205-5p and vascular endothelial growth factor (VEGFA) in bladder cancer tissues and their effects on the proliferation, migration and apoptosis.

Methods: Arraystar Human CircRNA chip was applied to analyzing the differential expression of circRNA in four bladder cancer tissues and paired adjacent normal bladder tissues. Real time quantitative PCR was utilized to detect the expression of circ0001429 in tissue specimens. Bioinformatics, RNA immunoprecipitation and luciferase reporter assays were used to verify the relationship among circ0001429, miR-205-5p and VEGFA in bladder cancer. Cell propagation was determined by CCK8 assay and roles of circ0001429 and miR-205-5p in cell migration were verified with transwell migration assay. Flow cytometry and TUNEL staining were conducted to observe the impact on cell apoptosis ability. Xenograft experiment was also performed to validate the influence of circ0001429 on tumor growth in vivo.

Results: Expressions of circ0001429 and VEGFA were up-regulated, whereas miR-205-5p expression was down-regulated in bladder cancer tissues in comparison with paired adjacent normal bladder tissues. Circ0001429 enhanced the propagation and metastasis abilities of T24 cells and 5637 cells in vitro, but reduced cell apoptosis. In vivo experiments revealed the inhibitor role of sh-circ0001429 in tumor growth and lung metastasis. Circ0001429 sponged miR-205-5p that targeted VEGFA, thereby modulating the protein level of VEGFA. Meanwhile, miR-205-5p restrained the cell viability and mobility and promoted the apoptosis in bladder cancer. Circ0001429 could accelerate cell propagation, migration and invasiveness through increasing VEGFA expression via miR-205-5p.

Conclusion: Circ0001429 and VEGFA were highly expressed in bladder cancer, while miR-205-5p were lowly expressed in bladder cancer. The circ0001429 could target at miR-205-5p to regulate VEGFA and promote the development of bladder cancer.

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