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circEVI5 acts as a miR-4793-3p sponge to suppress the proliferation of gastric cancer

Circular RNAs (circRNAs) are a novel class of endogenous noncoding RNAs (ncRNAs) with a covalently closed loop structure. Accumulating evidence shows that circRNAs play vital roles in the growth, metastasis, treatment and prognosis of various cancers. However, the detailed functions and underlying m...

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Autores principales: Yan, Meinan, Niu, Liling, Liu, Jing, Yao, Yuan, Li, Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8342614/
https://www.ncbi.nlm.nih.gov/pubmed/34354043
http://dx.doi.org/10.1038/s41419-021-04061-4
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author Yan, Meinan
Niu, Liling
Liu, Jing
Yao, Yuan
Li, Hui
author_facet Yan, Meinan
Niu, Liling
Liu, Jing
Yao, Yuan
Li, Hui
author_sort Yan, Meinan
collection PubMed
description Circular RNAs (circRNAs) are a novel class of endogenous noncoding RNAs (ncRNAs) with a covalently closed loop structure. Accumulating evidence shows that circRNAs play vital roles in the growth, metastasis, treatment and prognosis of various cancers. However, the detailed functions and underlying mechanisms of circEVI5 (hsa_circ_0013162) in gastric cancer (GC) remain undocumented. In this study, the expression levels and prognostic value of circEVI5 were validated in GC tissue samples by using qRT-PCR. circEVI5 was significantly downregulated in GC tissues and cells, and low circEVI5 expression was correlated with poor prognosis. Next, in vitro CCK-8 assay, EdU incorporation assay, PI staining cell cycle assay, and in vivo xenograft mouse models were conducted to assess the functions of circEVI5. Gain of function experiments indicated that circEVI5 could inhibit GC cell proliferation and retard the cell cycle. Moreover, bioinformatics prediction showed that circEVI5 binds to miR-4793-3p, while FOXO1 may be a target of miR-4793-3p. Pull-down assays, RNA immunoprecipitation (RIP) assays, luciferase assays, and western blot were used to confirm the interactions between circEVI5, miR-4793-3p, and FOXO1. Functional assays demonstrated that circEVI5 suppressed the proliferation of GC by sponging miR-4793-3p and increasing FOXO1 expression levels. In conclusion, our study demonstrated that circEVI5 can bind miR-4793-3p as a ceRNA to eliminate the negative regulation of FOXO1, therefore suppressing GC proliferation.
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spelling pubmed-83426142021-08-20 circEVI5 acts as a miR-4793-3p sponge to suppress the proliferation of gastric cancer Yan, Meinan Niu, Liling Liu, Jing Yao, Yuan Li, Hui Cell Death Dis Article Circular RNAs (circRNAs) are a novel class of endogenous noncoding RNAs (ncRNAs) with a covalently closed loop structure. Accumulating evidence shows that circRNAs play vital roles in the growth, metastasis, treatment and prognosis of various cancers. However, the detailed functions and underlying mechanisms of circEVI5 (hsa_circ_0013162) in gastric cancer (GC) remain undocumented. In this study, the expression levels and prognostic value of circEVI5 were validated in GC tissue samples by using qRT-PCR. circEVI5 was significantly downregulated in GC tissues and cells, and low circEVI5 expression was correlated with poor prognosis. Next, in vitro CCK-8 assay, EdU incorporation assay, PI staining cell cycle assay, and in vivo xenograft mouse models were conducted to assess the functions of circEVI5. Gain of function experiments indicated that circEVI5 could inhibit GC cell proliferation and retard the cell cycle. Moreover, bioinformatics prediction showed that circEVI5 binds to miR-4793-3p, while FOXO1 may be a target of miR-4793-3p. Pull-down assays, RNA immunoprecipitation (RIP) assays, luciferase assays, and western blot were used to confirm the interactions between circEVI5, miR-4793-3p, and FOXO1. Functional assays demonstrated that circEVI5 suppressed the proliferation of GC by sponging miR-4793-3p and increasing FOXO1 expression levels. In conclusion, our study demonstrated that circEVI5 can bind miR-4793-3p as a ceRNA to eliminate the negative regulation of FOXO1, therefore suppressing GC proliferation. Nature Publishing Group UK 2021-08-05 /pmc/articles/PMC8342614/ /pubmed/34354043 http://dx.doi.org/10.1038/s41419-021-04061-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Yan, Meinan
Niu, Liling
Liu, Jing
Yao, Yuan
Li, Hui
circEVI5 acts as a miR-4793-3p sponge to suppress the proliferation of gastric cancer
title circEVI5 acts as a miR-4793-3p sponge to suppress the proliferation of gastric cancer
title_full circEVI5 acts as a miR-4793-3p sponge to suppress the proliferation of gastric cancer
title_fullStr circEVI5 acts as a miR-4793-3p sponge to suppress the proliferation of gastric cancer
title_full_unstemmed circEVI5 acts as a miR-4793-3p sponge to suppress the proliferation of gastric cancer
title_short circEVI5 acts as a miR-4793-3p sponge to suppress the proliferation of gastric cancer
title_sort circevi5 acts as a mir-4793-3p sponge to suppress the proliferation of gastric cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8342614/
https://www.ncbi.nlm.nih.gov/pubmed/34354043
http://dx.doi.org/10.1038/s41419-021-04061-4
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