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Circular RNA_0074027 participates in cell proliferation, apoptosis and metastasis of colorectal cancer cells through regulation of miR-525-3p
The present study aimed to elucidate the biological function of circular RNAs (circRNA) 0074027 in colorectal cancer (CRC). The expression of circRNA-0074027 in CRC tissues and cells was determined by reverse transcription-quantitative PCR. The in vitro experiments, including Cell Counting Kit-8 (CC...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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D.A. Spandidos
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7974509/ https://www.ncbi.nlm.nih.gov/pubmed/33760126 http://dx.doi.org/10.3892/mmr.2021.11963 |
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author | Xiong, Gang Zhang, Jun Zhang, Yichao Pang, Xiao Wang, Biao Zhang, Yongchuan |
author_facet | Xiong, Gang Zhang, Jun Zhang, Yichao Pang, Xiao Wang, Biao Zhang, Yongchuan |
author_sort | Xiong, Gang |
collection | PubMed |
description | The present study aimed to elucidate the biological function of circular RNAs (circRNA) 0074027 in colorectal cancer (CRC). The expression of circRNA-0074027 in CRC tissues and cells was determined by reverse transcription-quantitative PCR. The in vitro experiments, including Cell Counting Kit-8 (CCK-8) assay, 5-Ethynyl-2′-deoxyuridine assay, flow cytometry and Transwell assay, were applied to evaluate cell proliferation, apoptosis and metastasis ability respectively following downregulation of circRNA-0074027. The correlation between circRNA-0074027 and micro (mi)RNA-525-3p was determined via dual-luciferase reporter assay. Finally, western blotting was used to explore the possible regulatory mechanism. CircRNA-0074027 was upregulated in CRC tissues, while miR-525-3p expression was reduced. In addition, patients with CRC and circRNA-0074027 overexpression were more likely to have low tumor differentiation, lymph node metastasis and advanced TMN stage. Deletion of circRNA-0074027 could suppress cell proliferation and metastasis through upregulating p53 expression and forbidding epithelial-mesenchymal transition signaling pathway. The addition of miRNA-525-3p inhibitors could reverse the anti-tumor effects induced by the deletion of circRNA-0074027. The downregulation of cirRNA_0074027 inhibited tumor progression via sponging miR-525-3p, which could be a promising treatment bio-marker for CRC. |
format | Online Article Text |
id | pubmed-7974509 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-79745092021-03-24 Circular RNA_0074027 participates in cell proliferation, apoptosis and metastasis of colorectal cancer cells through regulation of miR-525-3p Xiong, Gang Zhang, Jun Zhang, Yichao Pang, Xiao Wang, Biao Zhang, Yongchuan Mol Med Rep Articles The present study aimed to elucidate the biological function of circular RNAs (circRNA) 0074027 in colorectal cancer (CRC). The expression of circRNA-0074027 in CRC tissues and cells was determined by reverse transcription-quantitative PCR. The in vitro experiments, including Cell Counting Kit-8 (CCK-8) assay, 5-Ethynyl-2′-deoxyuridine assay, flow cytometry and Transwell assay, were applied to evaluate cell proliferation, apoptosis and metastasis ability respectively following downregulation of circRNA-0074027. The correlation between circRNA-0074027 and micro (mi)RNA-525-3p was determined via dual-luciferase reporter assay. Finally, western blotting was used to explore the possible regulatory mechanism. CircRNA-0074027 was upregulated in CRC tissues, while miR-525-3p expression was reduced. In addition, patients with CRC and circRNA-0074027 overexpression were more likely to have low tumor differentiation, lymph node metastasis and advanced TMN stage. Deletion of circRNA-0074027 could suppress cell proliferation and metastasis through upregulating p53 expression and forbidding epithelial-mesenchymal transition signaling pathway. The addition of miRNA-525-3p inhibitors could reverse the anti-tumor effects induced by the deletion of circRNA-0074027. The downregulation of cirRNA_0074027 inhibited tumor progression via sponging miR-525-3p, which could be a promising treatment bio-marker for CRC. D.A. Spandidos 2021-05 2021-03-05 /pmc/articles/PMC7974509/ /pubmed/33760126 http://dx.doi.org/10.3892/mmr.2021.11963 Text en Copyright: © Xiong et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , 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 | Articles Xiong, Gang Zhang, Jun Zhang, Yichao Pang, Xiao Wang, Biao Zhang, Yongchuan Circular RNA_0074027 participates in cell proliferation, apoptosis and metastasis of colorectal cancer cells through regulation of miR-525-3p |
title | Circular RNA_0074027 participates in cell proliferation, apoptosis and metastasis of colorectal cancer cells through regulation of miR-525-3p |
title_full | Circular RNA_0074027 participates in cell proliferation, apoptosis and metastasis of colorectal cancer cells through regulation of miR-525-3p |
title_fullStr | Circular RNA_0074027 participates in cell proliferation, apoptosis and metastasis of colorectal cancer cells through regulation of miR-525-3p |
title_full_unstemmed | Circular RNA_0074027 participates in cell proliferation, apoptosis and metastasis of colorectal cancer cells through regulation of miR-525-3p |
title_short | Circular RNA_0074027 participates in cell proliferation, apoptosis and metastasis of colorectal cancer cells through regulation of miR-525-3p |
title_sort | circular rna_0074027 participates in cell proliferation, apoptosis and metastasis of colorectal cancer cells through regulation of mir-525-3p |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7974509/ https://www.ncbi.nlm.nih.gov/pubmed/33760126 http://dx.doi.org/10.3892/mmr.2021.11963 |
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