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MiR-20a-5p promotes radio-resistance by targeting NPAS2 in nasopharyngeal cancer cells

MicroRNAs (miRNAs) are key players of gene expression involved in diverse biological processes including the cancer radio-resistance, which hinders the effective cancer therapy. Here we found that the miR-20a-5p level is significantly up-regulated in radio-resistant nasopharyngeal cancer (NPC) cells...

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Detalles Bibliográficos
Autores principales: Zhao, Fangfang, Pu, Youguang, Qian, Liting, Zang, Chunbao, Tao, Zhenchao, Gao, Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5739686/
https://www.ncbi.nlm.nih.gov/pubmed/29285299
http://dx.doi.org/10.18632/oncotarget.22411
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author Zhao, Fangfang
Pu, Youguang
Qian, Liting
Zang, Chunbao
Tao, Zhenchao
Gao, Jin
author_facet Zhao, Fangfang
Pu, Youguang
Qian, Liting
Zang, Chunbao
Tao, Zhenchao
Gao, Jin
author_sort Zhao, Fangfang
collection PubMed
description MicroRNAs (miRNAs) are key players of gene expression involved in diverse biological processes including the cancer radio-resistance, which hinders the effective cancer therapy. Here we found that the miR-20a-5p level is significantly up-regulated in radio-resistant nasopharyngeal cancer (NPC) cells via an RNA-seq and miR-omic analysis. Moreover, we identified that the neuronal PAS domain protein 2 (NPAS2) gene is one of the targets of miR-20a-5p. The involvement of miR-20a-5p and NPAS2 with NPC radio-resistance was further validated by either down- or up-regulation of their levels in NPC cell lines. Taken together, these results not only reveal novel insights into the NPC radio-resistance, but also provide hints for an effective therapeutic strategy to fight against NPC radio-resistance.
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spelling pubmed-57396862017-12-28 MiR-20a-5p promotes radio-resistance by targeting NPAS2 in nasopharyngeal cancer cells Zhao, Fangfang Pu, Youguang Qian, Liting Zang, Chunbao Tao, Zhenchao Gao, Jin Oncotarget Research Paper MicroRNAs (miRNAs) are key players of gene expression involved in diverse biological processes including the cancer radio-resistance, which hinders the effective cancer therapy. Here we found that the miR-20a-5p level is significantly up-regulated in radio-resistant nasopharyngeal cancer (NPC) cells via an RNA-seq and miR-omic analysis. Moreover, we identified that the neuronal PAS domain protein 2 (NPAS2) gene is one of the targets of miR-20a-5p. The involvement of miR-20a-5p and NPAS2 with NPC radio-resistance was further validated by either down- or up-regulation of their levels in NPC cell lines. Taken together, these results not only reveal novel insights into the NPC radio-resistance, but also provide hints for an effective therapeutic strategy to fight against NPC radio-resistance. Impact Journals LLC 2017-11-11 /pmc/articles/PMC5739686/ /pubmed/29285299 http://dx.doi.org/10.18632/oncotarget.22411 Text en Copyright: © 2017 Zhao et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Research Paper
Zhao, Fangfang
Pu, Youguang
Qian, Liting
Zang, Chunbao
Tao, Zhenchao
Gao, Jin
MiR-20a-5p promotes radio-resistance by targeting NPAS2 in nasopharyngeal cancer cells
title MiR-20a-5p promotes radio-resistance by targeting NPAS2 in nasopharyngeal cancer cells
title_full MiR-20a-5p promotes radio-resistance by targeting NPAS2 in nasopharyngeal cancer cells
title_fullStr MiR-20a-5p promotes radio-resistance by targeting NPAS2 in nasopharyngeal cancer cells
title_full_unstemmed MiR-20a-5p promotes radio-resistance by targeting NPAS2 in nasopharyngeal cancer cells
title_short MiR-20a-5p promotes radio-resistance by targeting NPAS2 in nasopharyngeal cancer cells
title_sort mir-20a-5p promotes radio-resistance by targeting npas2 in nasopharyngeal cancer cells
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5739686/
https://www.ncbi.nlm.nih.gov/pubmed/29285299
http://dx.doi.org/10.18632/oncotarget.22411
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