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Hypoxia-specific targets in cancer therapy: role of splice variants

Tumour hypoxia is a well known adverse prognostic factor in the treatment of solid tumours. Hypoxia-inducible factor 1α (HIF-1α), a transcription factor subunit regulating a large number of hypoxia-responsive genes, is considered an attractive target for novel treatment approaches, due to a frequent...

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Detalles Bibliográficos
Autor principal: Vordermark, Dirk
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2909930/
https://www.ncbi.nlm.nih.gov/pubmed/20624302
http://dx.doi.org/10.1186/1741-7015-8-45
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author Vordermark, Dirk
author_facet Vordermark, Dirk
author_sort Vordermark, Dirk
collection PubMed
description Tumour hypoxia is a well known adverse prognostic factor in the treatment of solid tumours. Hypoxia-inducible factor 1α (HIF-1α), a transcription factor subunit regulating a large number of hypoxia-responsive genes, is considered an attractive target for novel treatment approaches, due to a frequently reported association between HIF-1α overexpression and poor outcome in clinical series. This month in BMC Medicine, Dales et al. report on splice variants of HIF-1α in fresh frozen tissue samples of early human breast cancer, finding an association of mRNA levels of the variant HIF-1α(TAG )with adverse clinical factors (lymph node status, hormone receptor status) and poor metastasis-free survival. This preliminary study addresses the possibility that specific targeting of individual isoforms resulting from alternative splicing may play a role in HIF-1-directed treatment approaches. See research article: http://www.biomedcentral.com/1741-7015/8/44
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spelling pubmed-29099302010-07-27 Hypoxia-specific targets in cancer therapy: role of splice variants Vordermark, Dirk BMC Med Commentary Tumour hypoxia is a well known adverse prognostic factor in the treatment of solid tumours. Hypoxia-inducible factor 1α (HIF-1α), a transcription factor subunit regulating a large number of hypoxia-responsive genes, is considered an attractive target for novel treatment approaches, due to a frequently reported association between HIF-1α overexpression and poor outcome in clinical series. This month in BMC Medicine, Dales et al. report on splice variants of HIF-1α in fresh frozen tissue samples of early human breast cancer, finding an association of mRNA levels of the variant HIF-1α(TAG )with adverse clinical factors (lymph node status, hormone receptor status) and poor metastasis-free survival. This preliminary study addresses the possibility that specific targeting of individual isoforms resulting from alternative splicing may play a role in HIF-1-directed treatment approaches. See research article: http://www.biomedcentral.com/1741-7015/8/44 BioMed Central 2010-07-12 /pmc/articles/PMC2909930/ /pubmed/20624302 http://dx.doi.org/10.1186/1741-7015-8-45 Text en Copyright ©2010 Vordermark; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Commentary
Vordermark, Dirk
Hypoxia-specific targets in cancer therapy: role of splice variants
title Hypoxia-specific targets in cancer therapy: role of splice variants
title_full Hypoxia-specific targets in cancer therapy: role of splice variants
title_fullStr Hypoxia-specific targets in cancer therapy: role of splice variants
title_full_unstemmed Hypoxia-specific targets in cancer therapy: role of splice variants
title_short Hypoxia-specific targets in cancer therapy: role of splice variants
title_sort hypoxia-specific targets in cancer therapy: role of splice variants
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2909930/
https://www.ncbi.nlm.nih.gov/pubmed/20624302
http://dx.doi.org/10.1186/1741-7015-8-45
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