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Aspirin-induced long non-coding RNA suppresses colon cancer growth

BACKGROUND: To study the effect of long non-coding RNAs (lncRNA) on aspirin-treated colon cancer cells. METHODS: To study the changes of lncRNA in aspirin-treated colon cells by microarray analysis, real-time quantitative PCR (qPCR) was used to verify the expression of selected lncRNA and mRNA. The...

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Autores principales: Chen, Mingwei, Wu, Lili, Zhan, Huajie, Liu, Tonghua, He, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798653/
https://www.ncbi.nlm.nih.gov/pubmed/35116527
http://dx.doi.org/10.21037/tcr-20-2248
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author Chen, Mingwei
Wu, Lili
Zhan, Huajie
Liu, Tonghua
He, Yan
author_facet Chen, Mingwei
Wu, Lili
Zhan, Huajie
Liu, Tonghua
He, Yan
author_sort Chen, Mingwei
collection PubMed
description BACKGROUND: To study the effect of long non-coding RNAs (lncRNA) on aspirin-treated colon cancer cells. METHODS: To study the changes of lncRNA in aspirin-treated colon cells by microarray analysis, real-time quantitative PCR (qPCR) was used to verify the expression of selected lncRNA and mRNA. The effects of aspirin on the proliferation and metastasis of the siRNA transfected cells and control colon cancer cells were detected by Cell Counting Kit-8 (CCK-8) and Transwell experiments. Bioinformatics tools were employed to analyze the potential function of lncRNA. RESULTS: Compared with the control group, aspirin inhibited the proliferation and metastasis of colon cancer cells. Microarray analysis showed that a total of 10,568 lncRNAs and 22,126 mRNAs were noticeably expressed in the aspirin-treated group (≥1.5-fold, P<0.05). The qPCR results showed that lncRNA and mRNA expressions were consistent with microarray analysis. The analysis of the co-expression network profiles of 58 lncRNA and 101 mRNA differential genes showed a total of 158 nodes and 791 connections. Analysis of Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways revealed that a variety of lncRNAs (NEAT1, LOC152578) were involved in the inhibition mechanism of aspirin in colon cancer. CONCLUSIONS: lncRNA NEAT1 and LOC152578 are involved in the inhibition of tumor cell growth and metastasis by aspirin. The results of these analyses will help us further understand the mechanism of action of aspirin and the roles of lncRNAs in the prevention and treatment of colon cancer.
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spelling pubmed-87986532022-02-02 Aspirin-induced long non-coding RNA suppresses colon cancer growth Chen, Mingwei Wu, Lili Zhan, Huajie Liu, Tonghua He, Yan Transl Cancer Res Original Article BACKGROUND: To study the effect of long non-coding RNAs (lncRNA) on aspirin-treated colon cancer cells. METHODS: To study the changes of lncRNA in aspirin-treated colon cells by microarray analysis, real-time quantitative PCR (qPCR) was used to verify the expression of selected lncRNA and mRNA. The effects of aspirin on the proliferation and metastasis of the siRNA transfected cells and control colon cancer cells were detected by Cell Counting Kit-8 (CCK-8) and Transwell experiments. Bioinformatics tools were employed to analyze the potential function of lncRNA. RESULTS: Compared with the control group, aspirin inhibited the proliferation and metastasis of colon cancer cells. Microarray analysis showed that a total of 10,568 lncRNAs and 22,126 mRNAs were noticeably expressed in the aspirin-treated group (≥1.5-fold, P<0.05). The qPCR results showed that lncRNA and mRNA expressions were consistent with microarray analysis. The analysis of the co-expression network profiles of 58 lncRNA and 101 mRNA differential genes showed a total of 158 nodes and 791 connections. Analysis of Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways revealed that a variety of lncRNAs (NEAT1, LOC152578) were involved in the inhibition mechanism of aspirin in colon cancer. CONCLUSIONS: lncRNA NEAT1 and LOC152578 are involved in the inhibition of tumor cell growth and metastasis by aspirin. The results of these analyses will help us further understand the mechanism of action of aspirin and the roles of lncRNAs in the prevention and treatment of colon cancer. AME Publishing Company 2021-05 /pmc/articles/PMC8798653/ /pubmed/35116527 http://dx.doi.org/10.21037/tcr-20-2248 Text en 2021 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
spellingShingle Original Article
Chen, Mingwei
Wu, Lili
Zhan, Huajie
Liu, Tonghua
He, Yan
Aspirin-induced long non-coding RNA suppresses colon cancer growth
title Aspirin-induced long non-coding RNA suppresses colon cancer growth
title_full Aspirin-induced long non-coding RNA suppresses colon cancer growth
title_fullStr Aspirin-induced long non-coding RNA suppresses colon cancer growth
title_full_unstemmed Aspirin-induced long non-coding RNA suppresses colon cancer growth
title_short Aspirin-induced long non-coding RNA suppresses colon cancer growth
title_sort aspirin-induced long non-coding rna suppresses colon cancer growth
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798653/
https://www.ncbi.nlm.nih.gov/pubmed/35116527
http://dx.doi.org/10.21037/tcr-20-2248
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