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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2014
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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. |
format | Online Article Text |
id | pubmed-4253447 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
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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