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circRNA_103615 contributes to tumor progression and cisplatin resistance in NSCLC by regulating ABCB1

Lung cancer is one of the main causes of tumor lethality worldwide. Circular RNAs (circRNAs) have essential roles in tumor progression. However, in non-small cell lung carcinoma (NSCLC), the role of circRNAs remains unknown. In the present study, the expression, function and molecular mechanisms of...

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Autores principales: Liang, Hongguang, Lin, Zelong, Lin, Huiwen, Zhao, Li, Huang, Weihua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8281253/
https://www.ncbi.nlm.nih.gov/pubmed/34306203
http://dx.doi.org/10.3892/etm.2021.10366
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author Liang, Hongguang
Lin, Zelong
Lin, Huiwen
Zhao, Li
Huang, Weihua
author_facet Liang, Hongguang
Lin, Zelong
Lin, Huiwen
Zhao, Li
Huang, Weihua
author_sort Liang, Hongguang
collection PubMed
description Lung cancer is one of the main causes of tumor lethality worldwide. Circular RNAs (circRNAs) have essential roles in tumor progression. However, in non-small cell lung carcinoma (NSCLC), the role of circRNAs remains unknown. In the present study, the expression, function and molecular mechanisms of a new circRNA, circRNA_103615, were investigated in NSCLC. Reverse transcription-quantitative PCR (RT-qPCR) was used to detect circRNA_103615 expression levels in NSCLC and normal tissues, as well as in NSCLC cell lines. MTT assay, flow cytometric assay, colony formation assay, and cell migration and invasion assays were used to examine the function of circRNA_103615 in NSCLC cells. MTT assay, colony formation assay, RT-qPCR, and western blotting were used to detect the effect of circRNA_103615 on cisplatin resistance. The results demonstrated that NSCLC cell lines and tissues had increased levels of circRNA_103615 compared with normal cells and normal tissues, respectively. Functionally, silencing of circRNA_103615 by small interfering RNA resulted in suppression of cell growth, migration, and invasion, but promotion of cell apoptosis. In addition, the cisplatin resistance of NSCLC was reversed by the silencing of circRNA_103615. Notably, ATP binding cassette subfamily Bmember 1 (ABCB1) expression was significantly decreased following circRNA_103615 knockdown, and ABCB1 overexpression reversed the effects of circRNA_103615 silencing on NSCLC cisplatin resistance. Thus, the present study indicated that circRNA_103615 may serve as a critical oncogene and potential novel biomarker in NSCLC, as well as a potential cisplatin resistance promoter, by regulating ABCB1 expression.
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spelling pubmed-82812532021-07-22 circRNA_103615 contributes to tumor progression and cisplatin resistance in NSCLC by regulating ABCB1 Liang, Hongguang Lin, Zelong Lin, Huiwen Zhao, Li Huang, Weihua Exp Ther Med Articles Lung cancer is one of the main causes of tumor lethality worldwide. Circular RNAs (circRNAs) have essential roles in tumor progression. However, in non-small cell lung carcinoma (NSCLC), the role of circRNAs remains unknown. In the present study, the expression, function and molecular mechanisms of a new circRNA, circRNA_103615, were investigated in NSCLC. Reverse transcription-quantitative PCR (RT-qPCR) was used to detect circRNA_103615 expression levels in NSCLC and normal tissues, as well as in NSCLC cell lines. MTT assay, flow cytometric assay, colony formation assay, and cell migration and invasion assays were used to examine the function of circRNA_103615 in NSCLC cells. MTT assay, colony formation assay, RT-qPCR, and western blotting were used to detect the effect of circRNA_103615 on cisplatin resistance. The results demonstrated that NSCLC cell lines and tissues had increased levels of circRNA_103615 compared with normal cells and normal tissues, respectively. Functionally, silencing of circRNA_103615 by small interfering RNA resulted in suppression of cell growth, migration, and invasion, but promotion of cell apoptosis. In addition, the cisplatin resistance of NSCLC was reversed by the silencing of circRNA_103615. Notably, ATP binding cassette subfamily Bmember 1 (ABCB1) expression was significantly decreased following circRNA_103615 knockdown, and ABCB1 overexpression reversed the effects of circRNA_103615 silencing on NSCLC cisplatin resistance. Thus, the present study indicated that circRNA_103615 may serve as a critical oncogene and potential novel biomarker in NSCLC, as well as a potential cisplatin resistance promoter, by regulating ABCB1 expression. D.A. Spandidos 2021-09 2021-07-01 /pmc/articles/PMC8281253/ /pubmed/34306203 http://dx.doi.org/10.3892/etm.2021.10366 Text en Copyright: © Liang et al. https://creativecommons.org/licenses/by-nc-nd/4.0/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
Liang, Hongguang
Lin, Zelong
Lin, Huiwen
Zhao, Li
Huang, Weihua
circRNA_103615 contributes to tumor progression and cisplatin resistance in NSCLC by regulating ABCB1
title circRNA_103615 contributes to tumor progression and cisplatin resistance in NSCLC by regulating ABCB1
title_full circRNA_103615 contributes to tumor progression and cisplatin resistance in NSCLC by regulating ABCB1
title_fullStr circRNA_103615 contributes to tumor progression and cisplatin resistance in NSCLC by regulating ABCB1
title_full_unstemmed circRNA_103615 contributes to tumor progression and cisplatin resistance in NSCLC by regulating ABCB1
title_short circRNA_103615 contributes to tumor progression and cisplatin resistance in NSCLC by regulating ABCB1
title_sort circrna_103615 contributes to tumor progression and cisplatin resistance in nsclc by regulating abcb1
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8281253/
https://www.ncbi.nlm.nih.gov/pubmed/34306203
http://dx.doi.org/10.3892/etm.2021.10366
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