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miR-382 inhibits tumor growth and enhance chemosensitivity in osteosarcoma

Dysregulation of miRNAs is involved in osteosarcoma (OS). Here, we demonstrate that miR-382 is decreased in specimens of OS patients with a poor chemoresponse compared to those with a good chemoresponse. In addition, our clinical data show that decreased miR-382 was associated with poor survival in...

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Autores principales: Xu, Meng, Jin, Hua, Xu, Cheng-Xiong, Sun, Bo, Mao, Zhi, Bi, Wen-Zhi, Wang, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4253447/
https://www.ncbi.nlm.nih.gov/pubmed/25344865
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author Xu, Meng
Jin, Hua
Xu, Cheng-Xiong
Sun, Bo
Mao, Zhi
Bi, Wen-Zhi
Wang, Yan
author_facet Xu, Meng
Jin, Hua
Xu, Cheng-Xiong
Sun, Bo
Mao, Zhi
Bi, Wen-Zhi
Wang, Yan
author_sort Xu, Meng
collection PubMed
description Dysregulation of miRNAs is involved in osteosarcoma (OS). Here, we demonstrate that miR-382 is decreased in specimens of OS patients with a poor chemoresponse compared to those with a good chemoresponse. In addition, our clinical data show that decreased miR-382 was associated with poor survival in OS patients. Overexpression of miR-382 inhibited cell growth and chemoresistance by targeting KLF12 and HIPK3, respectively. In contrast, inhibition of miR-382 or overexpression of target genes stimulated OS cell growth and chemoresistance both in vitro and in vivo. Taken together, these findings suggest that miR-382 is a tumor suppressor miRNA and induction of miR-382 is a potential strategy to inhibit OS progression.
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spelling pubmed-42534472014-12-03 miR-382 inhibits tumor growth and enhance chemosensitivity in osteosarcoma Xu, Meng Jin, Hua Xu, Cheng-Xiong Sun, Bo Mao, Zhi Bi, Wen-Zhi Wang, Yan Oncotarget Research Paper Dysregulation of miRNAs is involved in osteosarcoma (OS). Here, we demonstrate that miR-382 is decreased in specimens of OS patients with a poor chemoresponse compared to those with a good chemoresponse. In addition, our clinical data show that decreased miR-382 was associated with poor survival in OS patients. Overexpression of miR-382 inhibited cell growth and chemoresistance by targeting KLF12 and HIPK3, respectively. In contrast, inhibition of miR-382 or overexpression of target genes stimulated OS cell growth and chemoresistance both in vitro and in vivo. Taken together, these findings suggest that miR-382 is a tumor suppressor miRNA and induction of miR-382 is a potential strategy to inhibit OS progression. Impact Journals LLC 2014-09-06 /pmc/articles/PMC4253447/ /pubmed/25344865 Text en Copyright: © 2014 Xu et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
spellingShingle Research Paper
Xu, Meng
Jin, Hua
Xu, Cheng-Xiong
Sun, Bo
Mao, Zhi
Bi, Wen-Zhi
Wang, Yan
miR-382 inhibits tumor growth and enhance chemosensitivity in osteosarcoma
title miR-382 inhibits tumor growth and enhance chemosensitivity in osteosarcoma
title_full miR-382 inhibits tumor growth and enhance chemosensitivity in osteosarcoma
title_fullStr miR-382 inhibits tumor growth and enhance chemosensitivity in osteosarcoma
title_full_unstemmed miR-382 inhibits tumor growth and enhance chemosensitivity in osteosarcoma
title_short miR-382 inhibits tumor growth and enhance chemosensitivity in osteosarcoma
title_sort mir-382 inhibits tumor growth and enhance chemosensitivity in osteosarcoma
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4253447/
https://www.ncbi.nlm.nih.gov/pubmed/25344865
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