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Iron Metabolism in Cancer

Demanded as an essential trace element that supports cell growth and basic functions, iron can be harmful and cancerogenic though. By exchanging between its different oxidized forms, iron overload induces free radical formation, lipid peroxidation, DNA, and protein damages, leading to carcinogenesis...

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Detalles Bibliográficos
Autores principales: Wang, Yafang, Yu, Lei, Ding, Jian, Chen, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6337236/
https://www.ncbi.nlm.nih.gov/pubmed/30591630
http://dx.doi.org/10.3390/ijms20010095
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author Wang, Yafang
Yu, Lei
Ding, Jian
Chen, Yi
author_facet Wang, Yafang
Yu, Lei
Ding, Jian
Chen, Yi
author_sort Wang, Yafang
collection PubMed
description Demanded as an essential trace element that supports cell growth and basic functions, iron can be harmful and cancerogenic though. By exchanging between its different oxidized forms, iron overload induces free radical formation, lipid peroxidation, DNA, and protein damages, leading to carcinogenesis or ferroptosis. Iron also plays profound roles in modulating tumor microenvironment and metastasis, maintaining genomic stability and controlling epigenetics. in order to meet the high requirement of iron, neoplastic cells have remodeled iron metabolism pathways, including acquisition, storage, and efflux, which makes manipulating iron homeostasis a considerable approach for cancer therapy. Several iron chelators and iron oxide nanoparticles (IONPs) has recently been developed for cancer intervention and presented considerable effects. This review summarizes some latest findings about iron metabolism function and regulation mechanism in cancer and the application of iron chelators and IONPs in cancer diagnosis and therapy.
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spelling pubmed-63372362019-01-22 Iron Metabolism in Cancer Wang, Yafang Yu, Lei Ding, Jian Chen, Yi Int J Mol Sci Review Demanded as an essential trace element that supports cell growth and basic functions, iron can be harmful and cancerogenic though. By exchanging between its different oxidized forms, iron overload induces free radical formation, lipid peroxidation, DNA, and protein damages, leading to carcinogenesis or ferroptosis. Iron also plays profound roles in modulating tumor microenvironment and metastasis, maintaining genomic stability and controlling epigenetics. in order to meet the high requirement of iron, neoplastic cells have remodeled iron metabolism pathways, including acquisition, storage, and efflux, which makes manipulating iron homeostasis a considerable approach for cancer therapy. Several iron chelators and iron oxide nanoparticles (IONPs) has recently been developed for cancer intervention and presented considerable effects. This review summarizes some latest findings about iron metabolism function and regulation mechanism in cancer and the application of iron chelators and IONPs in cancer diagnosis and therapy. MDPI 2018-12-27 /pmc/articles/PMC6337236/ /pubmed/30591630 http://dx.doi.org/10.3390/ijms20010095 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Wang, Yafang
Yu, Lei
Ding, Jian
Chen, Yi
Iron Metabolism in Cancer
title Iron Metabolism in Cancer
title_full Iron Metabolism in Cancer
title_fullStr Iron Metabolism in Cancer
title_full_unstemmed Iron Metabolism in Cancer
title_short Iron Metabolism in Cancer
title_sort iron metabolism in cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6337236/
https://www.ncbi.nlm.nih.gov/pubmed/30591630
http://dx.doi.org/10.3390/ijms20010095
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