CircCDYL Acts as a Tumor Suppressor in Wilms’ Tumor by Targeting miR-145-5p

Circular RNAs (circRNA) have been reported to exert evident functions in many human carcinomas. However, the possible mechanisms concerning the circRNA in various tumors are still elusive. In this research, we analyzed the expression profile and biological functions of circular RNA CDYL (circCDYL, c...

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Main Authors: Rui Zhou, Wei Jia, Xiaofeng Gao, Fuming Deng, Kai Fu, Tianxin Zhao, Zhongmin Li, Wen Fu, Guochang Liu
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-08-01
Series:Frontiers in Cell and Developmental Biology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fcell.2021.668947/full
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author Rui Zhou
Wei Jia
Xiaofeng Gao
Fuming Deng
Kai Fu
Tianxin Zhao
Zhongmin Li
Wen Fu
Guochang Liu
author_facet Rui Zhou
Wei Jia
Xiaofeng Gao
Fuming Deng
Kai Fu
Tianxin Zhao
Zhongmin Li
Wen Fu
Guochang Liu
author_sort Rui Zhou
collection DOAJ
description Circular RNAs (circRNA) have been reported to exert evident functions in many human carcinomas. However, the possible mechanisms concerning the circRNA in various tumors are still elusive. In this research, we analyzed the expression profile and biological functions of circular RNA CDYL (circCDYL, circBase ID: hsa_circ_0008285) in Wilms’ tumor. Here, miRNA and gene expression were examined by real-time PCR in Wilms’ tumor tissues and cell lines. The functions of circCDYL and its potential targets to influence cell proliferation, migration, and invasion in Wilms’ tumor cells were determined by biological functional experiments in vitro and in vivo. We predicted and analyzed potential miRNA targets through online bioinformatic tools. To validate the interactions between circCDYL and its targets, we performed RNA fluorescence in situ hybridization, biotin-coupled miRNA capture assay, and biotin-coupled probe pull-down assay. Tight junction protein l (TJP1) was proved to be the target gene of the predicted miRNA by dual-luciferase reporter assay. The expression level of TJP1 in Wilms’ tumor cells was identified via Western blot. We showed that circCDYL was downregulated in WT tissue compared with adjacent non-tumor tissue. Upregulation of circCDYL could reduce cell proliferation, migration, and invasion. Mechanically, circCDYL, functioning as a miRNA sponge, decreased the expression level of miR-145-5p and TJP1 3′UTR was validated as the target of miR-145-5p, facilitating the circCDYL/miR-145-5p/TJP1 axis. In conclusion, our study suggested circCDYL as a novel biomarker and therapeutic target for WT treatment.
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spelling doaj.art-d73c7c77823c4ff784bc6438f2b2d5c52022-12-21T22:32:14ZengFrontiers Media S.A.Frontiers in Cell and Developmental Biology2296-634X2021-08-01910.3389/fcell.2021.668947668947CircCDYL Acts as a Tumor Suppressor in Wilms’ Tumor by Targeting miR-145-5pRui ZhouWei JiaXiaofeng GaoFuming DengKai FuTianxin ZhaoZhongmin LiWen FuGuochang LiuCircular RNAs (circRNA) have been reported to exert evident functions in many human carcinomas. However, the possible mechanisms concerning the circRNA in various tumors are still elusive. In this research, we analyzed the expression profile and biological functions of circular RNA CDYL (circCDYL, circBase ID: hsa_circ_0008285) in Wilms’ tumor. Here, miRNA and gene expression were examined by real-time PCR in Wilms’ tumor tissues and cell lines. The functions of circCDYL and its potential targets to influence cell proliferation, migration, and invasion in Wilms’ tumor cells were determined by biological functional experiments in vitro and in vivo. We predicted and analyzed potential miRNA targets through online bioinformatic tools. To validate the interactions between circCDYL and its targets, we performed RNA fluorescence in situ hybridization, biotin-coupled miRNA capture assay, and biotin-coupled probe pull-down assay. Tight junction protein l (TJP1) was proved to be the target gene of the predicted miRNA by dual-luciferase reporter assay. The expression level of TJP1 in Wilms’ tumor cells was identified via Western blot. We showed that circCDYL was downregulated in WT tissue compared with adjacent non-tumor tissue. Upregulation of circCDYL could reduce cell proliferation, migration, and invasion. Mechanically, circCDYL, functioning as a miRNA sponge, decreased the expression level of miR-145-5p and TJP1 3′UTR was validated as the target of miR-145-5p, facilitating the circCDYL/miR-145-5p/TJP1 axis. In conclusion, our study suggested circCDYL as a novel biomarker and therapeutic target for WT treatment.https://www.frontiersin.org/articles/10.3389/fcell.2021.668947/fullmicroRNAtight junction protein 1Wilms’ tumorcircular RNAmir-145-5pbiomarker
spellingShingle Rui Zhou
Wei Jia
Xiaofeng Gao
Fuming Deng
Kai Fu
Tianxin Zhao
Zhongmin Li
Wen Fu
Guochang Liu
CircCDYL Acts as a Tumor Suppressor in Wilms’ Tumor by Targeting miR-145-5p
Frontiers in Cell and Developmental Biology
microRNA
tight junction protein 1
Wilms’ tumor
circular RNA
mir-145-5p
biomarker
title CircCDYL Acts as a Tumor Suppressor in Wilms’ Tumor by Targeting miR-145-5p
title_full CircCDYL Acts as a Tumor Suppressor in Wilms’ Tumor by Targeting miR-145-5p
title_fullStr CircCDYL Acts as a Tumor Suppressor in Wilms’ Tumor by Targeting miR-145-5p
title_full_unstemmed CircCDYL Acts as a Tumor Suppressor in Wilms’ Tumor by Targeting miR-145-5p
title_short CircCDYL Acts as a Tumor Suppressor in Wilms’ Tumor by Targeting miR-145-5p
title_sort circcdyl acts as a tumor suppressor in wilms tumor by targeting mir 145 5p
topic microRNA
tight junction protein 1
Wilms’ tumor
circular RNA
mir-145-5p
biomarker
url https://www.frontiersin.org/articles/10.3389/fcell.2021.668947/full
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