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Differential regulation of hepcidin in cancer and non-cancer tissues and its clinical implications
Hepcidin is a crucial peptide for regulating cellular iron efflux. Because iron is essential for cell survival, especially for highly active cells, such as tumor cells, it is imperative to understand how tumor cells manipulate hepcidin expression for their own metabolic needs. Studies suggest that h...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5903825/ https://www.ncbi.nlm.nih.gov/pubmed/29391539 http://dx.doi.org/10.1038/emm.2017.273 |
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author | Vela, Driton Vela-Gaxha, Zana |
author_facet | Vela, Driton Vela-Gaxha, Zana |
author_sort | Vela, Driton |
collection | PubMed |
description | Hepcidin is a crucial peptide for regulating cellular iron efflux. Because iron is essential for cell survival, especially for highly active cells, such as tumor cells, it is imperative to understand how tumor cells manipulate hepcidin expression for their own metabolic needs. Studies suggest that hepcidin expression and regulation in tumor cells show important differences in comparison with those in non-tumorous cells. These differences should be investigated to develop new strategies to fight cancer cells. Manipulating hepcidin expression to starve cancer cells for iron may prove to be a new therapy in the anticancer arsenal. |
format | Online Article Text |
id | pubmed-5903825 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-59038252018-04-19 Differential regulation of hepcidin in cancer and non-cancer tissues and its clinical implications Vela, Driton Vela-Gaxha, Zana Exp Mol Med Review Hepcidin is a crucial peptide for regulating cellular iron efflux. Because iron is essential for cell survival, especially for highly active cells, such as tumor cells, it is imperative to understand how tumor cells manipulate hepcidin expression for their own metabolic needs. Studies suggest that hepcidin expression and regulation in tumor cells show important differences in comparison with those in non-tumorous cells. These differences should be investigated to develop new strategies to fight cancer cells. Manipulating hepcidin expression to starve cancer cells for iron may prove to be a new therapy in the anticancer arsenal. Nature Publishing Group 2018-02 2018-02-02 /pmc/articles/PMC5903825/ /pubmed/29391539 http://dx.doi.org/10.1038/emm.2017.273 Text en Copyright © 2018 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | Review Vela, Driton Vela-Gaxha, Zana Differential regulation of hepcidin in cancer and non-cancer tissues and its clinical implications |
title | Differential regulation of hepcidin in cancer and non-cancer tissues and its clinical implications |
title_full | Differential regulation of hepcidin in cancer and non-cancer tissues and its clinical implications |
title_fullStr | Differential regulation of hepcidin in cancer and non-cancer tissues and its clinical implications |
title_full_unstemmed | Differential regulation of hepcidin in cancer and non-cancer tissues and its clinical implications |
title_short | Differential regulation of hepcidin in cancer and non-cancer tissues and its clinical implications |
title_sort | differential regulation of hepcidin in cancer and non-cancer tissues and its clinical implications |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5903825/ https://www.ncbi.nlm.nih.gov/pubmed/29391539 http://dx.doi.org/10.1038/emm.2017.273 |
work_keys_str_mv | AT veladriton differentialregulationofhepcidinincancerandnoncancertissuesanditsclinicalimplications AT velagaxhazana differentialregulationofhepcidinincancerandnoncancertissuesanditsclinicalimplications |