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MicroRNA-573 inhibits cell proliferation, migration, and invasion and is downregulated by PICSAR in cutaneous squamous cell carcinoma

The incidence of cutaneous squamous cell carcinoma (cSCC) has been increasing in recent years. Meanwhile, microRNAs have been found to play vital roles in various cancers, including cSCC. This study aimed to investigate the expression of microRNA-573 (miR-573) in cSCC, its relationship with long non...

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Autores principales: Wang, Yanhua, Tang, Shengjian, Jianping, L. V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Association of Basic Medical Sciences of Federation of Bosnia and Herzegovina 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8977082/
https://www.ncbi.nlm.nih.gov/pubmed/34905724
http://dx.doi.org/10.17305/bjbms.2021.6301
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author Wang, Yanhua
Tang, Shengjian
Jianping, L. V.
author_facet Wang, Yanhua
Tang, Shengjian
Jianping, L. V.
author_sort Wang, Yanhua
collection PubMed
description The incidence of cutaneous squamous cell carcinoma (cSCC) has been increasing in recent years. Meanwhile, microRNAs have been found to play vital roles in various cancers, including cSCC. This study aimed to investigate the expression of microRNA-573 (miR-573) in cSCC, its relationship with long non-coding RNA PICSAR and analyze its biological role. The relationship between PICSAR and miR-573 was confirmed by dual-luciferase reporter assay and Pearson’s correlation coefficient analysis. The levels of PICSAR and miR-573 were measured using quantitative Real-Time polymerase chain reaction. Cell Counting Kit-8 assay was used to evaluate the cSCC cell proliferation ability. The migration and invasion abilities of cSCC cells were evaluated by Transwell assay. PICSAR expression was increased and miR-573 was decreased in tumor tissues and cSCC cell lines. PICSAR and miR-573 can bind directly, and miR-573 expression was downregulated by PICSAR in cSCC. Overexpression of miR-573 significantly inhibited the proliferation, migration, and invasion abilities of A431 and SCC13 cells. In addition, miR-573 overexpression reversed the promotion effects of PICSAR overexpression on cSCC cell proliferation, migration, and invasion abilities. In conclusion, our findings indicated that miR-573 expression was decreased in tumor tissues and cSCC cells and was downregulated by PICSAR in cSCC. Additionally, miR-573 overexpression inhibited cSCC cell proliferation, migration and invasion, and reversed the promotion effects of PICSAR overexpression on cSCC cell biological functions. Thus, miR-573 might function as a tumor suppressor and might be involved in the regulatory effects of PICSAR on tumorigenesis in cSCC.
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spelling pubmed-89770822022-04-14 MicroRNA-573 inhibits cell proliferation, migration, and invasion and is downregulated by PICSAR in cutaneous squamous cell carcinoma Wang, Yanhua Tang, Shengjian Jianping, L. V. Bosn J Basic Med Sci Research Article The incidence of cutaneous squamous cell carcinoma (cSCC) has been increasing in recent years. Meanwhile, microRNAs have been found to play vital roles in various cancers, including cSCC. This study aimed to investigate the expression of microRNA-573 (miR-573) in cSCC, its relationship with long non-coding RNA PICSAR and analyze its biological role. The relationship between PICSAR and miR-573 was confirmed by dual-luciferase reporter assay and Pearson’s correlation coefficient analysis. The levels of PICSAR and miR-573 were measured using quantitative Real-Time polymerase chain reaction. Cell Counting Kit-8 assay was used to evaluate the cSCC cell proliferation ability. The migration and invasion abilities of cSCC cells were evaluated by Transwell assay. PICSAR expression was increased and miR-573 was decreased in tumor tissues and cSCC cell lines. PICSAR and miR-573 can bind directly, and miR-573 expression was downregulated by PICSAR in cSCC. Overexpression of miR-573 significantly inhibited the proliferation, migration, and invasion abilities of A431 and SCC13 cells. In addition, miR-573 overexpression reversed the promotion effects of PICSAR overexpression on cSCC cell proliferation, migration, and invasion abilities. In conclusion, our findings indicated that miR-573 expression was decreased in tumor tissues and cSCC cells and was downregulated by PICSAR in cSCC. Additionally, miR-573 overexpression inhibited cSCC cell proliferation, migration and invasion, and reversed the promotion effects of PICSAR overexpression on cSCC cell biological functions. Thus, miR-573 might function as a tumor suppressor and might be involved in the regulatory effects of PICSAR on tumorigenesis in cSCC. Association of Basic Medical Sciences of Federation of Bosnia and Herzegovina 2022-04 2021-12-06 /pmc/articles/PMC8977082/ /pubmed/34905724 http://dx.doi.org/10.17305/bjbms.2021.6301 Text en Copyright: © The Author(s) (2022) https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License
spellingShingle Research Article
Wang, Yanhua
Tang, Shengjian
Jianping, L. V.
MicroRNA-573 inhibits cell proliferation, migration, and invasion and is downregulated by PICSAR in cutaneous squamous cell carcinoma
title MicroRNA-573 inhibits cell proliferation, migration, and invasion and is downregulated by PICSAR in cutaneous squamous cell carcinoma
title_full MicroRNA-573 inhibits cell proliferation, migration, and invasion and is downregulated by PICSAR in cutaneous squamous cell carcinoma
title_fullStr MicroRNA-573 inhibits cell proliferation, migration, and invasion and is downregulated by PICSAR in cutaneous squamous cell carcinoma
title_full_unstemmed MicroRNA-573 inhibits cell proliferation, migration, and invasion and is downregulated by PICSAR in cutaneous squamous cell carcinoma
title_short MicroRNA-573 inhibits cell proliferation, migration, and invasion and is downregulated by PICSAR in cutaneous squamous cell carcinoma
title_sort microrna-573 inhibits cell proliferation, migration, and invasion and is downregulated by picsar in cutaneous squamous cell carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8977082/
https://www.ncbi.nlm.nih.gov/pubmed/34905724
http://dx.doi.org/10.17305/bjbms.2021.6301
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