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Hypoxia response and microRNAs: no longer two separate worlds
MicroRNAs (miRs) are short non-coding transcripts involved in a wide variety of cellular processes. Several recent studies have established a link between hypoxia, a well-documented component of the tumour microenvironment, and specific miRs. One member of this class, miR-210, was identified as hypo...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3918058/ https://www.ncbi.nlm.nih.gov/pubmed/18624759 http://dx.doi.org/10.1111/j.1582-4934.2008.00398.x |
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author | Ivan, Mircea Harris, Adrian L Martelli, Fabio Kulshreshtha, Ritu |
author_facet | Ivan, Mircea Harris, Adrian L Martelli, Fabio Kulshreshtha, Ritu |
author_sort | Ivan, Mircea |
collection | PubMed |
description | MicroRNAs (miRs) are short non-coding transcripts involved in a wide variety of cellular processes. Several recent studies have established a link between hypoxia, a well-documented component of the tumour microenvironment, and specific miRs. One member of this class, miR-210, was identified as hypoxia inducible in all the cell types tested, and is overexpressed in most cancer types. Its hypoxic induction is dependent on a functional hypoxia-inducible factor (HIF), thus extending the transcriptional repertoire of the latter beyond ‘classic’ genes. From a clinical standpoint, miR-210 overexpression has been associated with adverse prognosis in breast tumours and been detected in serum of lymphoma patients and could serve as a tool to define hypoxic malignancies. We discuss the role of miR-210 and its emerging targets, as well as possible future directions for clinical applications in oncology and ischaemic disorders. |
format | Online Article Text |
id | pubmed-3918058 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-39180582015-04-27 Hypoxia response and microRNAs: no longer two separate worlds Ivan, Mircea Harris, Adrian L Martelli, Fabio Kulshreshtha, Ritu J Cell Mol Med Reviews MicroRNAs (miRs) are short non-coding transcripts involved in a wide variety of cellular processes. Several recent studies have established a link between hypoxia, a well-documented component of the tumour microenvironment, and specific miRs. One member of this class, miR-210, was identified as hypoxia inducible in all the cell types tested, and is overexpressed in most cancer types. Its hypoxic induction is dependent on a functional hypoxia-inducible factor (HIF), thus extending the transcriptional repertoire of the latter beyond ‘classic’ genes. From a clinical standpoint, miR-210 overexpression has been associated with adverse prognosis in breast tumours and been detected in serum of lymphoma patients and could serve as a tool to define hypoxic malignancies. We discuss the role of miR-210 and its emerging targets, as well as possible future directions for clinical applications in oncology and ischaemic disorders. Blackwell Publishing Ltd 2008-09 2008-07-08 /pmc/articles/PMC3918058/ /pubmed/18624759 http://dx.doi.org/10.1111/j.1582-4934.2008.00398.x Text en © 2008 The Authors Journal compilation © 2008 Foundation for Cellular and Molecular Medicine/Blackwell Publishing Ltd |
spellingShingle | Reviews Ivan, Mircea Harris, Adrian L Martelli, Fabio Kulshreshtha, Ritu Hypoxia response and microRNAs: no longer two separate worlds |
title | Hypoxia response and microRNAs: no longer two separate worlds |
title_full | Hypoxia response and microRNAs: no longer two separate worlds |
title_fullStr | Hypoxia response and microRNAs: no longer two separate worlds |
title_full_unstemmed | Hypoxia response and microRNAs: no longer two separate worlds |
title_short | Hypoxia response and microRNAs: no longer two separate worlds |
title_sort | hypoxia response and micrornas: no longer two separate worlds |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3918058/ https://www.ncbi.nlm.nih.gov/pubmed/18624759 http://dx.doi.org/10.1111/j.1582-4934.2008.00398.x |
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