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Metadherin is an apoptotic modulator in prostate cancer through miR-342-3p regulation

Prostate cancer is the second most common cancer in men worldwide. This study focused to clarify the roles of Metadherin (MTDH) and miR-342-3p in prostate cancer. We identified that MTDH was up-regulated and miR-342-3p was down-regulated in the prostate tissues, and there is an inverse correlation b...

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Detalles Bibliográficos
Autores principales: Hu, Kebang, Mu, Xupeng, Kolibaba, Helena, Yin, Qinan, Liu, Chune, Liang, Xueqing, Lu, Ji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6088108/
https://www.ncbi.nlm.nih.gov/pubmed/30108450
http://dx.doi.org/10.1016/j.sjbs.2018.04.015
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author Hu, Kebang
Mu, Xupeng
Kolibaba, Helena
Yin, Qinan
Liu, Chune
Liang, Xueqing
Lu, Ji
author_facet Hu, Kebang
Mu, Xupeng
Kolibaba, Helena
Yin, Qinan
Liu, Chune
Liang, Xueqing
Lu, Ji
author_sort Hu, Kebang
collection PubMed
description Prostate cancer is the second most common cancer in men worldwide. This study focused to clarify the roles of Metadherin (MTDH) and miR-342-3p in prostate cancer. We identified that MTDH was up-regulated and miR-342-3p was down-regulated in the prostate tissues, and there is an inverse correlation between MTDH and miR-342-3p. Functional studies revealed that miR-342-3p directly targets MTDH via binding to the 3′ untranslated regions (UTRs) in the prostate cancer cells. Moreover, we also found MTDH overexpression in DU145 and PC3 cells inhibited apoptosis. Subsequently, miR-342-3p has been revealed to reverse the MTDH effect on the cellular apoptosis in the further studies. Our results indicate that MTDH repress apoptosis of prostate cancer in vitro and provides a new strategy for human prostate cancer therapy in the future.
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spelling pubmed-60881082018-08-14 Metadherin is an apoptotic modulator in prostate cancer through miR-342-3p regulation Hu, Kebang Mu, Xupeng Kolibaba, Helena Yin, Qinan Liu, Chune Liang, Xueqing Lu, Ji Saudi J Biol Sci Article Prostate cancer is the second most common cancer in men worldwide. This study focused to clarify the roles of Metadherin (MTDH) and miR-342-3p in prostate cancer. We identified that MTDH was up-regulated and miR-342-3p was down-regulated in the prostate tissues, and there is an inverse correlation between MTDH and miR-342-3p. Functional studies revealed that miR-342-3p directly targets MTDH via binding to the 3′ untranslated regions (UTRs) in the prostate cancer cells. Moreover, we also found MTDH overexpression in DU145 and PC3 cells inhibited apoptosis. Subsequently, miR-342-3p has been revealed to reverse the MTDH effect on the cellular apoptosis in the further studies. Our results indicate that MTDH repress apoptosis of prostate cancer in vitro and provides a new strategy for human prostate cancer therapy in the future. Elsevier 2018-07 2018-04-22 /pmc/articles/PMC6088108/ /pubmed/30108450 http://dx.doi.org/10.1016/j.sjbs.2018.04.015 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Hu, Kebang
Mu, Xupeng
Kolibaba, Helena
Yin, Qinan
Liu, Chune
Liang, Xueqing
Lu, Ji
Metadherin is an apoptotic modulator in prostate cancer through miR-342-3p regulation
title Metadherin is an apoptotic modulator in prostate cancer through miR-342-3p regulation
title_full Metadherin is an apoptotic modulator in prostate cancer through miR-342-3p regulation
title_fullStr Metadherin is an apoptotic modulator in prostate cancer through miR-342-3p regulation
title_full_unstemmed Metadherin is an apoptotic modulator in prostate cancer through miR-342-3p regulation
title_short Metadherin is an apoptotic modulator in prostate cancer through miR-342-3p regulation
title_sort metadherin is an apoptotic modulator in prostate cancer through mir-342-3p regulation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6088108/
https://www.ncbi.nlm.nih.gov/pubmed/30108450
http://dx.doi.org/10.1016/j.sjbs.2018.04.015
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