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Dexmedetomidine Inhibits Osteosarcoma Cell Proliferation and Migration, and Promotes Apoptosis by Regulating miR-520a-3p

This study aimed to investigate the effect of dexmedetomidine (DEX) on osteosarcoma (OS) cell line MG63 and to explore the possible relationship between DEX and miR-520-3p in OS. The results showed that DEX could upregulate miR-520-3p, which directly targeted AKT1. Additionally, miR-520-3p also inhi...

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Autores principales: Wang, Xiaoyan, Xu, Yongguang, Chen, Xinlei, Xiao, Jianmin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cognizant Communication Corporation 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7844699/
https://www.ncbi.nlm.nih.gov/pubmed/28653601
http://dx.doi.org/10.3727/096504017X14982578608217
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author Wang, Xiaoyan
Xu, Yongguang
Chen, Xinlei
Xiao, Jianmin
author_facet Wang, Xiaoyan
Xu, Yongguang
Chen, Xinlei
Xiao, Jianmin
author_sort Wang, Xiaoyan
collection PubMed
description This study aimed to investigate the effect of dexmedetomidine (DEX) on osteosarcoma (OS) cell line MG63 and to explore the possible relationship between DEX and miR-520-3p in OS. The results showed that DEX could upregulate miR-520-3p, which directly targeted AKT1. Additionally, miR-520-3p also inhibited MG63 cell proliferation and migration, promoted apoptosis, and suppressed protein expressions of AKT, p-AKT, p-mTOR, and p-ERK1/2. DEX can inhibit OS cell proliferation and migration and promote apoptosis by upregulating the expression level of miR-520a-3p. DEX may serve as a potential therapeutic agent in OS treatment, and miR-520a-3p may be a potential target in the therapy of OS.
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spelling pubmed-78446992021-02-16 Dexmedetomidine Inhibits Osteosarcoma Cell Proliferation and Migration, and Promotes Apoptosis by Regulating miR-520a-3p Wang, Xiaoyan Xu, Yongguang Chen, Xinlei Xiao, Jianmin Oncol Res Article This study aimed to investigate the effect of dexmedetomidine (DEX) on osteosarcoma (OS) cell line MG63 and to explore the possible relationship between DEX and miR-520-3p in OS. The results showed that DEX could upregulate miR-520-3p, which directly targeted AKT1. Additionally, miR-520-3p also inhibited MG63 cell proliferation and migration, promoted apoptosis, and suppressed protein expressions of AKT, p-AKT, p-mTOR, and p-ERK1/2. DEX can inhibit OS cell proliferation and migration and promote apoptosis by upregulating the expression level of miR-520a-3p. DEX may serve as a potential therapeutic agent in OS treatment, and miR-520a-3p may be a potential target in the therapy of OS. Cognizant Communication Corporation 2018-04-10 /pmc/articles/PMC7844699/ /pubmed/28653601 http://dx.doi.org/10.3727/096504017X14982578608217 Text en Copyright © 2018 Cognizant, LLC. http://creativecommons.org/licenses/by-nc-nd/4.0/ This article is licensed under a Creative Commons Attribution-NonCommercial NoDerivatives 4.0 International License.
spellingShingle Article
Wang, Xiaoyan
Xu, Yongguang
Chen, Xinlei
Xiao, Jianmin
Dexmedetomidine Inhibits Osteosarcoma Cell Proliferation and Migration, and Promotes Apoptosis by Regulating miR-520a-3p
title Dexmedetomidine Inhibits Osteosarcoma Cell Proliferation and Migration, and Promotes Apoptosis by Regulating miR-520a-3p
title_full Dexmedetomidine Inhibits Osteosarcoma Cell Proliferation and Migration, and Promotes Apoptosis by Regulating miR-520a-3p
title_fullStr Dexmedetomidine Inhibits Osteosarcoma Cell Proliferation and Migration, and Promotes Apoptosis by Regulating miR-520a-3p
title_full_unstemmed Dexmedetomidine Inhibits Osteosarcoma Cell Proliferation and Migration, and Promotes Apoptosis by Regulating miR-520a-3p
title_short Dexmedetomidine Inhibits Osteosarcoma Cell Proliferation and Migration, and Promotes Apoptosis by Regulating miR-520a-3p
title_sort dexmedetomidine inhibits osteosarcoma cell proliferation and migration, and promotes apoptosis by regulating mir-520a-3p
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7844699/
https://www.ncbi.nlm.nih.gov/pubmed/28653601
http://dx.doi.org/10.3727/096504017X14982578608217
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