Cargando…

CircRNA_0005075 suppresses carcinogenesis via regulating miR‐431/p53/epithelial‐mesenchymal transition axis in gastric cancer

This study was aimed to explore the expression and biological function of circRNA_0005075 in gastric cancer (GC) progression and its underlying mechanism. First, the expression level of circRNA_0005075 and microRNA‐431 (miR‐431) in GC tissues were detected with the quantitative real‐time polymerase...

Descripción completa

Detalles Bibliográficos
Autores principales: Wu, Jiaming, Chen, Zhiheng, Song, Yihuan, Zhu, Yi, Dou, Guangjian, Shen, Xuning, Zhou, Yuan, Jiang, Honggang, Li, Jin, Peng, Yuping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7587004/
https://www.ncbi.nlm.nih.gov/pubmed/32133664
http://dx.doi.org/10.1002/cbf.3519
_version_ 1783600104324726784
author Wu, Jiaming
Chen, Zhiheng
Song, Yihuan
Zhu, Yi
Dou, Guangjian
Shen, Xuning
Zhou, Yuan
Jiang, Honggang
Li, Jin
Peng, Yuping
author_facet Wu, Jiaming
Chen, Zhiheng
Song, Yihuan
Zhu, Yi
Dou, Guangjian
Shen, Xuning
Zhou, Yuan
Jiang, Honggang
Li, Jin
Peng, Yuping
author_sort Wu, Jiaming
collection PubMed
description This study was aimed to explore the expression and biological function of circRNA_0005075 in gastric cancer (GC) progression and its underlying mechanism. First, the expression level of circRNA_0005075 and microRNA‐431 (miR‐431) in GC tissues were detected with the quantitative real‐time polymerase chain reaction. In addition, after down‐regulated the circRNA_0005075 expression by plasmid transfection in GC cells, the Cell Counting Kit‐8 (CCK‐8), EDU, transwell assay were conducted to evaluate the function of circRNA_0005075 or miR‐431 on cell proliferation, metastasis in vitro. Moreover, p53 and Epithelial‐mesenchymal transition (EMT) pathway related proteins were also measured with western blotting. Then, our data revealed that CircRNA_0005075 was found to be significantly up‐regulated in GC tissues as well as GC cell lines, and the GC patients with higher CircRNA_0005075 expression were more likely to have poor outcomes. Down‐regulation of CircRNA_0005075 could significantly suppress the GC cell proliferation and cell metastasis ability, while the addition of miR‐431 inhibitors could counteract this effect. Importantly, we discovered that the silencing of circRNA_0005075 could weaken the micro‐RNA sponge function for miR‐431, and then upregulate the expression of p53 and forbid the EMT signalling pathway, and finally suppress the tumourigenesis of GC. To sum up, CircRNA_0005075 could inhibit cell growth and metastasis of GC through regulating the miR‐431/p53/EMT axis. SIGNIFICANCE OF THE STUDY: The research clearly elucidated the potential role and relative regulatory mechanism of circRNA_0005075 in gastric cancer (GC) progression. Briefly, circRNA_0005075 could directly inhibit the expression level of miR‐431, then regulate the p53/Epithelial‐mesenchymal transition axis, and finally inhibit cell growth and metastasis in GC. Consequently, circRNA_0005075 might act as an oncogene in the GC procession, which provides a promising way for the treatment of GC.
format Online
Article
Text
id pubmed-7587004
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-75870042020-10-30 CircRNA_0005075 suppresses carcinogenesis via regulating miR‐431/p53/epithelial‐mesenchymal transition axis in gastric cancer Wu, Jiaming Chen, Zhiheng Song, Yihuan Zhu, Yi Dou, Guangjian Shen, Xuning Zhou, Yuan Jiang, Honggang Li, Jin Peng, Yuping Cell Biochem Funct Research Articles This study was aimed to explore the expression and biological function of circRNA_0005075 in gastric cancer (GC) progression and its underlying mechanism. First, the expression level of circRNA_0005075 and microRNA‐431 (miR‐431) in GC tissues were detected with the quantitative real‐time polymerase chain reaction. In addition, after down‐regulated the circRNA_0005075 expression by plasmid transfection in GC cells, the Cell Counting Kit‐8 (CCK‐8), EDU, transwell assay were conducted to evaluate the function of circRNA_0005075 or miR‐431 on cell proliferation, metastasis in vitro. Moreover, p53 and Epithelial‐mesenchymal transition (EMT) pathway related proteins were also measured with western blotting. Then, our data revealed that CircRNA_0005075 was found to be significantly up‐regulated in GC tissues as well as GC cell lines, and the GC patients with higher CircRNA_0005075 expression were more likely to have poor outcomes. Down‐regulation of CircRNA_0005075 could significantly suppress the GC cell proliferation and cell metastasis ability, while the addition of miR‐431 inhibitors could counteract this effect. Importantly, we discovered that the silencing of circRNA_0005075 could weaken the micro‐RNA sponge function for miR‐431, and then upregulate the expression of p53 and forbid the EMT signalling pathway, and finally suppress the tumourigenesis of GC. To sum up, CircRNA_0005075 could inhibit cell growth and metastasis of GC through regulating the miR‐431/p53/EMT axis. SIGNIFICANCE OF THE STUDY: The research clearly elucidated the potential role and relative regulatory mechanism of circRNA_0005075 in gastric cancer (GC) progression. Briefly, circRNA_0005075 could directly inhibit the expression level of miR‐431, then regulate the p53/Epithelial‐mesenchymal transition axis, and finally inhibit cell growth and metastasis in GC. Consequently, circRNA_0005075 might act as an oncogene in the GC procession, which provides a promising way for the treatment of GC. John Wiley and Sons Inc. 2020-03-04 2020-10 /pmc/articles/PMC7587004/ /pubmed/32133664 http://dx.doi.org/10.1002/cbf.3519 Text en © 2020 The Authors. Cell Biochemistry and Function published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Wu, Jiaming
Chen, Zhiheng
Song, Yihuan
Zhu, Yi
Dou, Guangjian
Shen, Xuning
Zhou, Yuan
Jiang, Honggang
Li, Jin
Peng, Yuping
CircRNA_0005075 suppresses carcinogenesis via regulating miR‐431/p53/epithelial‐mesenchymal transition axis in gastric cancer
title CircRNA_0005075 suppresses carcinogenesis via regulating miR‐431/p53/epithelial‐mesenchymal transition axis in gastric cancer
title_full CircRNA_0005075 suppresses carcinogenesis via regulating miR‐431/p53/epithelial‐mesenchymal transition axis in gastric cancer
title_fullStr CircRNA_0005075 suppresses carcinogenesis via regulating miR‐431/p53/epithelial‐mesenchymal transition axis in gastric cancer
title_full_unstemmed CircRNA_0005075 suppresses carcinogenesis via regulating miR‐431/p53/epithelial‐mesenchymal transition axis in gastric cancer
title_short CircRNA_0005075 suppresses carcinogenesis via regulating miR‐431/p53/epithelial‐mesenchymal transition axis in gastric cancer
title_sort circrna_0005075 suppresses carcinogenesis via regulating mir‐431/p53/epithelial‐mesenchymal transition axis in gastric cancer
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7587004/
https://www.ncbi.nlm.nih.gov/pubmed/32133664
http://dx.doi.org/10.1002/cbf.3519
work_keys_str_mv AT wujiaming circrna0005075suppressescarcinogenesisviaregulatingmir431p53epithelialmesenchymaltransitionaxisingastriccancer
AT chenzhiheng circrna0005075suppressescarcinogenesisviaregulatingmir431p53epithelialmesenchymaltransitionaxisingastriccancer
AT songyihuan circrna0005075suppressescarcinogenesisviaregulatingmir431p53epithelialmesenchymaltransitionaxisingastriccancer
AT zhuyi circrna0005075suppressescarcinogenesisviaregulatingmir431p53epithelialmesenchymaltransitionaxisingastriccancer
AT douguangjian circrna0005075suppressescarcinogenesisviaregulatingmir431p53epithelialmesenchymaltransitionaxisingastriccancer
AT shenxuning circrna0005075suppressescarcinogenesisviaregulatingmir431p53epithelialmesenchymaltransitionaxisingastriccancer
AT zhouyuan circrna0005075suppressescarcinogenesisviaregulatingmir431p53epithelialmesenchymaltransitionaxisingastriccancer
AT jianghonggang circrna0005075suppressescarcinogenesisviaregulatingmir431p53epithelialmesenchymaltransitionaxisingastriccancer
AT lijin circrna0005075suppressescarcinogenesisviaregulatingmir431p53epithelialmesenchymaltransitionaxisingastriccancer
AT pengyuping circrna0005075suppressescarcinogenesisviaregulatingmir431p53epithelialmesenchymaltransitionaxisingastriccancer