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miR-193a-3p regulates the multi-drug resistance of bladder cancer by targeting the LOXL4 gene and the Oxidative Stress pathway

BACKGROUND: Chemoresistance is a major obstacle to the curative cancer chemotherapy and presents one of the most formidable challenges in both research and management of cancer. RESULTS: From the detailed studies of a multi-chemosensitive (5637) versus a chemoresistant (H-bc) bladder cancer cell lin...

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Autores principales: Deng, Hui, Lv, Lei, Li, Yang, Zhang, Cheng, Meng, Fang, Pu, Youguang, Xiao, Jun, Qian, Liting, Zhao, Weidong, Liu, Qi, Zhang, Daming, Wang, Yingwei, Zhang, Hongyu, He, Yinghua, Zhu, Jingde
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4200202/
https://www.ncbi.nlm.nih.gov/pubmed/25311867
http://dx.doi.org/10.1186/1476-4598-13-234
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author Deng, Hui
Lv, Lei
Li, Yang
Zhang, Cheng
Meng, Fang
Pu, Youguang
Xiao, Jun
Qian, Liting
Zhao, Weidong
Liu, Qi
Zhang, Daming
Wang, Yingwei
Zhang, Hongyu
He, Yinghua
Zhu, Jingde
author_facet Deng, Hui
Lv, Lei
Li, Yang
Zhang, Cheng
Meng, Fang
Pu, Youguang
Xiao, Jun
Qian, Liting
Zhao, Weidong
Liu, Qi
Zhang, Daming
Wang, Yingwei
Zhang, Hongyu
He, Yinghua
Zhu, Jingde
author_sort Deng, Hui
collection PubMed
description BACKGROUND: Chemoresistance is a major obstacle to the curative cancer chemotherapy and presents one of the most formidable challenges in both research and management of cancer. RESULTS: From the detailed studies of a multi-chemosensitive (5637) versus a chemoresistant (H-bc) bladder cancer cell lines, we showed that miR-193a-3p [GenBank: NR_029710.1] promotes the multi-chemoresistance of bladder cancer cells. We further demonstrated that lysyl oxidase-like 4 (LOXL4) gene [GenBank: NM_032211.6] is a direct target of miR-193a-3p and executes the former’s impact on bladder cancer chemoresistance. The Oxidative Stress pathway activity is drastically affected by a forced reversal of miR-193a-3p or LOXL4 levels in cell and may act at the downstream of LOXL4 gene to relay the miR-193a-3p’s impact on the multi-chemoresistance in both cultured cells and the tumor xenografts in nude mice. CONCLUSIONS: In addition to a new mechanistic insight, our results provide a set of the essential genes in this newly identified miR-193a-3p/LOXL4/Oxidative Stress axis as the diagnostic targets for a guided anti-bladder cancer chemotherapy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1476-4598-13-234) contains supplementary material, which is available to authorized users.
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spelling pubmed-42002022014-10-18 miR-193a-3p regulates the multi-drug resistance of bladder cancer by targeting the LOXL4 gene and the Oxidative Stress pathway Deng, Hui Lv, Lei Li, Yang Zhang, Cheng Meng, Fang Pu, Youguang Xiao, Jun Qian, Liting Zhao, Weidong Liu, Qi Zhang, Daming Wang, Yingwei Zhang, Hongyu He, Yinghua Zhu, Jingde Mol Cancer Research BACKGROUND: Chemoresistance is a major obstacle to the curative cancer chemotherapy and presents one of the most formidable challenges in both research and management of cancer. RESULTS: From the detailed studies of a multi-chemosensitive (5637) versus a chemoresistant (H-bc) bladder cancer cell lines, we showed that miR-193a-3p [GenBank: NR_029710.1] promotes the multi-chemoresistance of bladder cancer cells. We further demonstrated that lysyl oxidase-like 4 (LOXL4) gene [GenBank: NM_032211.6] is a direct target of miR-193a-3p and executes the former’s impact on bladder cancer chemoresistance. The Oxidative Stress pathway activity is drastically affected by a forced reversal of miR-193a-3p or LOXL4 levels in cell and may act at the downstream of LOXL4 gene to relay the miR-193a-3p’s impact on the multi-chemoresistance in both cultured cells and the tumor xenografts in nude mice. CONCLUSIONS: In addition to a new mechanistic insight, our results provide a set of the essential genes in this newly identified miR-193a-3p/LOXL4/Oxidative Stress axis as the diagnostic targets for a guided anti-bladder cancer chemotherapy. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1476-4598-13-234) contains supplementary material, which is available to authorized users. BioMed Central 2014-10-14 /pmc/articles/PMC4200202/ /pubmed/25311867 http://dx.doi.org/10.1186/1476-4598-13-234 Text en © Deng et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Deng, Hui
Lv, Lei
Li, Yang
Zhang, Cheng
Meng, Fang
Pu, Youguang
Xiao, Jun
Qian, Liting
Zhao, Weidong
Liu, Qi
Zhang, Daming
Wang, Yingwei
Zhang, Hongyu
He, Yinghua
Zhu, Jingde
miR-193a-3p regulates the multi-drug resistance of bladder cancer by targeting the LOXL4 gene and the Oxidative Stress pathway
title miR-193a-3p regulates the multi-drug resistance of bladder cancer by targeting the LOXL4 gene and the Oxidative Stress pathway
title_full miR-193a-3p regulates the multi-drug resistance of bladder cancer by targeting the LOXL4 gene and the Oxidative Stress pathway
title_fullStr miR-193a-3p regulates the multi-drug resistance of bladder cancer by targeting the LOXL4 gene and the Oxidative Stress pathway
title_full_unstemmed miR-193a-3p regulates the multi-drug resistance of bladder cancer by targeting the LOXL4 gene and the Oxidative Stress pathway
title_short miR-193a-3p regulates the multi-drug resistance of bladder cancer by targeting the LOXL4 gene and the Oxidative Stress pathway
title_sort mir-193a-3p regulates the multi-drug resistance of bladder cancer by targeting the loxl4 gene and the oxidative stress pathway
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4200202/
https://www.ncbi.nlm.nih.gov/pubmed/25311867
http://dx.doi.org/10.1186/1476-4598-13-234
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