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环状RNA circFUT8通过吸附miR-570-3p上调Krüpple样因子10以抑制膀胱癌转移。

circRNA circFUT8 Upregulates Krüpple-like Factor 10 to Inhibit the Metastasis of Bladder Cancer via Sponging miR-570-3p.

作者信息

He Qingqing, Yan Dong, Dong Wei, Bi Junming, Huang Lifang, Yang Meihua, Huang Jian, Qin Haide, Lin Tianxin

机构信息

Department of Urology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.

Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, Guangzhou, China.

出版信息

Mol Ther Oncolytics. 2020 Jan 11;16:172-187. doi: 10.1016/j.omto.2019.12.014. eCollection 2020 Mar 27.

Abstract

Circular RNAs (circRNAs) are broad and diverse endogenous non-coding RNAs. Emerging evidence has revealed that circRNAs play pivotal roles in cancers, regulating the gene expression by acting as a microRNA (miRNA) sponge. However, the biological functions of circRNAs in bladder cancer (BCa) remain largely unknown. In this study, we identified an altered circRNA, termed circFUT8, by screening RNA sequencing data generated from three BCa tissues and matched adjacent normal bladder tissues. Quantitative real-time PCR analysis demonstrated that circFUT8 was downregulated in BCa tissues and correlated with patients' prognosis, histological grade, and lymph node (LN) metastasis. Functionally, gain- and loss-of-function assays indicated that circFUT8 inhibited the migration and invasion of BCa cell lines and LN metastasis . Mechanistically, circFUT8 directly bound to miR-570-3p and partially abrogated its oncogenic role, and miR-570-3p could suppress the expression of tumor suppressor gene Krüpple-like factor 10 (KLF10) by binding its 3' untranslated region (3' UTR). Moreover, we found that circFUT8 promoted the expression of KLF10 by competitively sponging miR-570-3p. In conclusion, circFUT8 functions as a tumor suppressor in BCa cells by targeting the miR-570-3p/KLF10 axis and may serve as a potential biomarker and therapeutic target for the management of BCa patients with LN metastasis.

摘要

环状RNA(circRNAs)是广泛且多样的内源性非编码RNA。新出现的证据表明,circRNAs在癌症中发挥关键作用,通过充当微小RNA(miRNA)海绵来调节基因表达。然而,circRNAs在膀胱癌(BCa)中的生物学功能仍 largely未知。在本研究中,我们通过筛选来自三个BCa组织及匹配的相邻正常膀胱组织的RNA测序数据,鉴定出一种改变的circRNA,称为circFUT8。定量实时PCR分析表明,circFUT8在BCa组织中下调,且与患者的预后、组织学分级和淋巴结(LN)转移相关。在功能上,功能获得和功能丧失实验表明,circFUT8抑制BCa细胞系的迁移和侵袭以及LN转移。机制上,circFUT8直接与miR-570-3p结合并部分消除其致癌作用,且miR-570-3p可通过结合其3'非翻译区(3'UTR)来抑制肿瘤抑制基因Krüpple样因子10(KLF10)的表达。此外,我们发现circFUT8通过竞争性结合miR-570-3p来促进KLF10的表达。总之,circFUT8通过靶向miR-570-3p/KLF10轴在BCa细胞中发挥肿瘤抑制作用,并且可能作为有LN转移的BCa患者管理的潜在生物标志物和治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/965f/7013148/4cb111de9722/gr1.jpg

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