Circ_0000745通过调节miR-409-3p/ATF1轴促进宫颈癌的进展

Cancer biotherapy & radiopharmaceuticals Pub Date : 2022-11-01 Epub Date: 2020-07-09 DOI:10.1089/cbr.2019.3392
Xia Cui, Jiming Chen, Yafeng Zheng, Huaji Shen
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引用次数: 11

摘要

背景:宫颈癌是一种常见的妇科恶性肿瘤,复发率高,死亡率高。环状rna在肿瘤的发生和发展中起着至关重要的作用。本研究旨在探讨circ_0000745在CC中的功能和机制。材料和方法:采用实时定量聚合酶链反应或Western blot法检测circ_0000745、miR-409-3p和激活转录因子1 (ATF1)的水平。用菌落形成法测定细胞增殖情况。transwell法观察细胞的迁移和侵袭。通过测量细胞外酸化速率、葡萄糖摄取和乳酸生成来分析糖酵解。Western blot检测葡萄糖转运蛋白1和乳酸脱氢酶A的蛋白水平。circ_0000745、miR-409-3p和ATF1之间的关系通过双荧光素酶报告基因检测得到证实。此外,采用异种移植物实验分析肿瘤在体内的生长情况。结果:Circ_0000745和ATF1在CC组织和细胞中上调,而miR-409-3p则下调。敲低circ_0000745可抑制CC细胞的增殖、迁移、侵袭和糖酵解。Circ_0000745通过靶向miR-409-3p调节CC进展。Circ_0000745通过海绵miR-409-3p调节ATF1的表达。MiR-409-3p通过靶向ATF1阻碍CC进展。此外,circ_0000745的缺失阻碍了肿瘤在体内的生长。结论:Circ_0000745通过调节miR-409-3p/ATF1轴促进CC的进展,表明Circ_0000745是一种很有前景的CC治疗生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Circ_0000745 Promotes the Progression of Cervical Cancer by Regulating miR-409-3p/ATF1 Axis.

Background: Cervical cancer (CC) is a common gynecological malignancy with a high risk of recurrence and death. Circular RNAs play a crucial role in the occurrence and development of tumors. This study aimed to investigate the function and mechanism of circ_0000745 in CC. Materials and Methods: The levels of circ_0000745, miR-409-3p, and activating transcription factor 1 (ATF1) were determined by quantitative real-time polymerase chain reaction or Western blot assay. Cell proliferation was assessed by colony formation assay. Cell migration and invasion were evaluated by transwell assay. Glycolysis was analyzed by measuring extracellular acidification rate, glucose uptake, and lactate production. Also, the protein levels of glucose transporter 1 and lactate dehydrogenase A were detected using Western blot. The relationship among circ_0000745, miR-409-3p, and ATF1 were confirmed by dual-luciferase reporter assay. Moreover, xenograft assay was performed to analyze tumor growth in vivo. Results: Circ_0000745 and ATF1 were upregulated, whereas miR-409-3p was downregulated in CC tissues and cells. Knockdown of circ_0000745 repressed proliferation, migration, invasion, and glycolysis of CC cells. Circ_0000745 regulated CC progression by targeting miR-409-3p. Circ_0000745 modulated ATF1 expression through sponging miR-409-3p. MiR-409-3p hindered CC progression by targeting ATF1. Furthermore, depletion of circ_0000745 impeded tumor growth in vivo. Conclusion: Circ_0000745 promoted the progression of CC through modulating miR-409-3p/ATF1 axis, indicating a promising biomarker for CC therapy.

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