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Twist1 promotes radioresistance in nasopharyngeal carcinoma

With the development of advanced imaging and radiation technologies, radiotherapy has been employed as the principal treatment approach for nasopharyngeal carcinoma (NPC). So far, a number of patients still suffer from the failure of this treatment due to the acquired radioresistance, but the underl...

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Autores principales: Zhang, Linli, Su, Beibei, Sun, Wei, Li, Wenwen, Luo, Min, Liu, Dongbo, Mei, Qi, Long, Guoxian, Hu, Guangyuan, Hu, Guoqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5348396/
https://www.ncbi.nlm.nih.gov/pubmed/27793033
http://dx.doi.org/10.18632/oncotarget.12875
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author Zhang, Linli
Su, Beibei
Sun, Wei
Li, Wenwen
Luo, Min
Liu, Dongbo
Mei, Qi
Long, Guoxian
Hu, Guangyuan
Hu, Guoqing
author_facet Zhang, Linli
Su, Beibei
Sun, Wei
Li, Wenwen
Luo, Min
Liu, Dongbo
Mei, Qi
Long, Guoxian
Hu, Guangyuan
Hu, Guoqing
author_sort Zhang, Linli
collection PubMed
description With the development of advanced imaging and radiation technologies, radiotherapy has been employed as the principal treatment approach for nasopharyngeal carcinoma (NPC). So far, a number of patients still suffer from the failure of this treatment due to the acquired radioresistance, but the underlying mechanisms are still poorly defined. In this study, we found that Twist1, participating in a variety of cell biological process, was associated with the malignancy of NPC and could induce NPC radioresistance in vitro and in vivo. Mechanically, Twist1 could promote the accumulation of DNA damage repair and inhibit the apoptosis of NPC cells. Therefore, our study not only elucidates the significant role of Twist1 in radioresistance of NPC, but also highlights Twist1 as a potential therapeutic target for NPC.
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spelling pubmed-53483962017-03-31 Twist1 promotes radioresistance in nasopharyngeal carcinoma Zhang, Linli Su, Beibei Sun, Wei Li, Wenwen Luo, Min Liu, Dongbo Mei, Qi Long, Guoxian Hu, Guangyuan Hu, Guoqing Oncotarget Research Paper With the development of advanced imaging and radiation technologies, radiotherapy has been employed as the principal treatment approach for nasopharyngeal carcinoma (NPC). So far, a number of patients still suffer from the failure of this treatment due to the acquired radioresistance, but the underlying mechanisms are still poorly defined. In this study, we found that Twist1, participating in a variety of cell biological process, was associated with the malignancy of NPC and could induce NPC radioresistance in vitro and in vivo. Mechanically, Twist1 could promote the accumulation of DNA damage repair and inhibit the apoptosis of NPC cells. Therefore, our study not only elucidates the significant role of Twist1 in radioresistance of NPC, but also highlights Twist1 as a potential therapeutic target for NPC. Impact Journals LLC 2016-10-25 /pmc/articles/PMC5348396/ /pubmed/27793033 http://dx.doi.org/10.18632/oncotarget.12875 Text en Copyright: © 2016 Zhang et al. http://creativecommons.org/licenses/by/3.0/ 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
Zhang, Linli
Su, Beibei
Sun, Wei
Li, Wenwen
Luo, Min
Liu, Dongbo
Mei, Qi
Long, Guoxian
Hu, Guangyuan
Hu, Guoqing
Twist1 promotes radioresistance in nasopharyngeal carcinoma
title Twist1 promotes radioresistance in nasopharyngeal carcinoma
title_full Twist1 promotes radioresistance in nasopharyngeal carcinoma
title_fullStr Twist1 promotes radioresistance in nasopharyngeal carcinoma
title_full_unstemmed Twist1 promotes radioresistance in nasopharyngeal carcinoma
title_short Twist1 promotes radioresistance in nasopharyngeal carcinoma
title_sort twist1 promotes radioresistance in nasopharyngeal carcinoma
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5348396/
https://www.ncbi.nlm.nih.gov/pubmed/27793033
http://dx.doi.org/10.18632/oncotarget.12875
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