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Multiple functions of hypoxia-regulated miR-210 in cancer

MicroRNAs (miRNAs) are small noncoding RNAs that regulate gene expression post-transcriptionally. miRNAs can be induced by a variety of stresses such as hypoxia, and are involved in diverse biological processes including differentiation, cell proliferation, cell death, and tumorigenesis. Hypoxia, a...

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Detalles Bibliográficos
Autores principales: Qin, Qin, Furong, Wei, Baosheng, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4060094/
https://www.ncbi.nlm.nih.gov/pubmed/24909053
http://dx.doi.org/10.1186/1756-9966-33-50
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author Qin, Qin
Furong, Wei
Baosheng, Li
author_facet Qin, Qin
Furong, Wei
Baosheng, Li
author_sort Qin, Qin
collection PubMed
description MicroRNAs (miRNAs) are small noncoding RNAs that regulate gene expression post-transcriptionally. miRNAs can be induced by a variety of stresses such as hypoxia, and are involved in diverse biological processes including differentiation, cell proliferation, cell death, and tumorigenesis. Hypoxia, a common feature of tumor microenvironment, can induce a number of miRNAs expression. miRNA-210 (miR-210) is one of the hypoxia-regulated-miRNAs, which has been investigated extensively in cancer. However, paradoxically opposing results were documented regarding whether it is an oncogene or a tumor suppressor, and whether it is a positive or negative prognostic biomarker. In the present review, we focus on the following investigations of miR-210: 1) its functions of as an oncogene, 2) its functions as a tumor suppressor, 3) its functions in mitochondrial metabolism, and finally, the diagnostic and prognostic value of miR-210 in cancer researches.
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spelling pubmed-40600942014-06-18 Multiple functions of hypoxia-regulated miR-210 in cancer Qin, Qin Furong, Wei Baosheng, Li J Exp Clin Cancer Res Review MicroRNAs (miRNAs) are small noncoding RNAs that regulate gene expression post-transcriptionally. miRNAs can be induced by a variety of stresses such as hypoxia, and are involved in diverse biological processes including differentiation, cell proliferation, cell death, and tumorigenesis. Hypoxia, a common feature of tumor microenvironment, can induce a number of miRNAs expression. miRNA-210 (miR-210) is one of the hypoxia-regulated-miRNAs, which has been investigated extensively in cancer. However, paradoxically opposing results were documented regarding whether it is an oncogene or a tumor suppressor, and whether it is a positive or negative prognostic biomarker. In the present review, we focus on the following investigations of miR-210: 1) its functions of as an oncogene, 2) its functions as a tumor suppressor, 3) its functions in mitochondrial metabolism, and finally, the diagnostic and prognostic value of miR-210 in cancer researches. BioMed Central 2014-06-09 /pmc/articles/PMC4060094/ /pubmed/24909053 http://dx.doi.org/10.1186/1756-9966-33-50 Text en Copyright © 2014 Qin et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/4.0 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 Review
Qin, Qin
Furong, Wei
Baosheng, Li
Multiple functions of hypoxia-regulated miR-210 in cancer
title Multiple functions of hypoxia-regulated miR-210 in cancer
title_full Multiple functions of hypoxia-regulated miR-210 in cancer
title_fullStr Multiple functions of hypoxia-regulated miR-210 in cancer
title_full_unstemmed Multiple functions of hypoxia-regulated miR-210 in cancer
title_short Multiple functions of hypoxia-regulated miR-210 in cancer
title_sort multiple functions of hypoxia-regulated mir-210 in cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4060094/
https://www.ncbi.nlm.nih.gov/pubmed/24909053
http://dx.doi.org/10.1186/1756-9966-33-50
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