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Iron at the Interface of Hepatocellular Carcinoma

Cancer incidence and mortality are rapidly growing, with liver cancer being the sixth most diagnosed cancer worldwide and the third leading cause of cancer death in 2020. A number of risk factors have been identified that trigger the progression to hepatocellular carcinoma. In this review, we focus...

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Detalles Bibliográficos
Autores principales: Paganoni, Rossana, Lechel, André, Vujic Spasic, Maja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8071427/
https://www.ncbi.nlm.nih.gov/pubmed/33921027
http://dx.doi.org/10.3390/ijms22084097
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author Paganoni, Rossana
Lechel, André
Vujic Spasic, Maja
author_facet Paganoni, Rossana
Lechel, André
Vujic Spasic, Maja
author_sort Paganoni, Rossana
collection PubMed
description Cancer incidence and mortality are rapidly growing, with liver cancer being the sixth most diagnosed cancer worldwide and the third leading cause of cancer death in 2020. A number of risk factors have been identified that trigger the progression to hepatocellular carcinoma. In this review, we focus on iron as a potential risk factor for liver carcinogenesis. Molecules involved in the regulation of iron metabolism are often upregulated in cancer cells, in order to provide a supply of this essential trace element for all stages of tumor development, survival, proliferation, and metastasis. Thus, cellular and systemic iron levels must be tightly regulated to prevent or delay liver cancer progression. Disorders associated with dysregulated iron metabolism are characterized with increased susceptibility to hepatocellular carcinoma. This review discusses the association of iron with metabolic disorders such as hereditary hemochromatosis, non-alcoholic fatty liver disease, obesity, and type 2 diabetes, in the background of hepatocellular carcinoma.
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spelling pubmed-80714272021-04-26 Iron at the Interface of Hepatocellular Carcinoma Paganoni, Rossana Lechel, André Vujic Spasic, Maja Int J Mol Sci Review Cancer incidence and mortality are rapidly growing, with liver cancer being the sixth most diagnosed cancer worldwide and the third leading cause of cancer death in 2020. A number of risk factors have been identified that trigger the progression to hepatocellular carcinoma. In this review, we focus on iron as a potential risk factor for liver carcinogenesis. Molecules involved in the regulation of iron metabolism are often upregulated in cancer cells, in order to provide a supply of this essential trace element for all stages of tumor development, survival, proliferation, and metastasis. Thus, cellular and systemic iron levels must be tightly regulated to prevent or delay liver cancer progression. Disorders associated with dysregulated iron metabolism are characterized with increased susceptibility to hepatocellular carcinoma. This review discusses the association of iron with metabolic disorders such as hereditary hemochromatosis, non-alcoholic fatty liver disease, obesity, and type 2 diabetes, in the background of hepatocellular carcinoma. MDPI 2021-04-15 /pmc/articles/PMC8071427/ /pubmed/33921027 http://dx.doi.org/10.3390/ijms22084097 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Paganoni, Rossana
Lechel, André
Vujic Spasic, Maja
Iron at the Interface of Hepatocellular Carcinoma
title Iron at the Interface of Hepatocellular Carcinoma
title_full Iron at the Interface of Hepatocellular Carcinoma
title_fullStr Iron at the Interface of Hepatocellular Carcinoma
title_full_unstemmed Iron at the Interface of Hepatocellular Carcinoma
title_short Iron at the Interface of Hepatocellular Carcinoma
title_sort iron at the interface of hepatocellular carcinoma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8071427/
https://www.ncbi.nlm.nih.gov/pubmed/33921027
http://dx.doi.org/10.3390/ijms22084097
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