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环状核因子IX通过海绵化微小RNA-34a-5p,经由细胞周期蛋白B1促进垂体腺瘤进展。

CircNFIX promotes progression of pituitary adenoma via CCNB1 by sponging miR-34a -5p.

作者信息

Cheng Jianhua, Nie Ding, Li Bin, Gui SongBai, Li ChuZhong, Zhang YaZhuo, Zhao Peng

机构信息

Neurosurgical Department, Beijing Tiantan Hospital, Capital Medical University, Beijing, 100070, China.

Department of Cell and Biology, Beijing Neurosurgical Institute, Beijing, 100070, China.

出版信息

Mol Cell Endocrinol. 2021 Apr 5;525:111140. doi: 10.1016/j.mce.2020.111140. Epub 2021 Feb 9.

Abstract

Previous studies have shown that CCNB1 affects the invasiveness of pituitary adenomas, and it is of great significance to find the upstream mechanism of regulating CCNB1.In this study, we explored a significantly overexpressed circRNA in invasive pituitary adenomas. Based on bioinformatics analysis and mechanism experiments, we determined that circNFIX (has-circ_0005660) affects cell invasion, migration and proliferation in pituitary adenomas by sponging miR-34a-5p through CCNB1. In pituitary adenoma tissues, the expression of circNFIX and CCNB1 was upregulated, while miR-34a-5p expression was downregulated. The silencing of circNFIX or overexpression of miR-34a-5p inhibited cell invasion, migration and proliferation. Inhibition of miR-34a-5p expression reversed the inhibitory effect of circNFIX silencing on the progression of pituitary adenoma. In conclusion, CircNFIX affects cell invasion, migration, and proliferation in pituitary adenomas by sponging miR-34a-5p through CCNB1. Therefore, circNFIX is expected to serve as a potential target for the treatment of pituitary adenomas.

摘要

以往研究表明,CCNB1影响垂体腺瘤的侵袭性,因此寻找调控CCNB1的上游机制具有重要意义。在本研究中,我们在侵袭性垂体腺瘤中发现了一种显著高表达的环状RNA。基于生物信息学分析和机制实验,我们确定环状核因子IX(circNFIX,即has-circ_0005660)通过CCNB1海绵吸附miR-34a-5p影响垂体腺瘤细胞的侵袭、迁移和增殖。在垂体腺瘤组织中,circNFIX和CCNB1的表达上调,而miR-34a-5p的表达下调。circNFIX沉默或miR-34a-5p过表达可抑制细胞侵袭、迁移和增殖。抑制miR-34a-5p表达可逆转circNFIX沉默对垂体腺瘤进展的抑制作用。综上所述,circNFIX通过CCNB1海绵吸附miR-34a-5p影响垂体腺瘤细胞的侵袭、迁移和增殖。因此,circNFIX有望成为治疗垂体腺瘤的潜在靶点。

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