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Iron: a target for the management of Kaposi's sarcoma?

BACKGROUND: Kaposi's sarcoma (KS) is a mesenchymal tumour associated with human herpesvirus-8 infection. However, the incidence of human herpesvirus-8 infection is far higher than the prevalence of KS, suggesting that viral infection per se is not sufficient for the development of malignancy an...

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Autor principal: Simonart, Thierry
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC317471/
https://www.ncbi.nlm.nih.gov/pubmed/14725718
http://dx.doi.org/10.1186/1471-2407-4-1
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author Simonart, Thierry
author_facet Simonart, Thierry
author_sort Simonart, Thierry
collection PubMed
description BACKGROUND: Kaposi's sarcoma (KS) is a mesenchymal tumour associated with human herpesvirus-8 infection. However, the incidence of human herpesvirus-8 infection is far higher than the prevalence of KS, suggesting that viral infection per se is not sufficient for the development of malignancy and that one or more additional cofactors are required. DISCUSSION: Epidemiological data suggest that iron may be one of the cofactors involved in the pathogenesis of KS. Iron is a well-known carcinogen and may favour KS growth through several pathways. Based on the apoptotic and antiproliferative effect of iron chelation on KS cells, it is suggested that iron withdrawal strategies could be developed for the management of KS. Studies using potent iron chelators in suitable KS animal models are critical to evaluate whether iron deprivation may be a useful anti-KS strategy. SUMMARY: It is suggested that iron may be one of non-viral co-factors involved of KS pathogenesis and that iron withdrawal strategies might interfere with tumour growth in patients with KS.
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spelling pubmed-3174712004-01-24 Iron: a target for the management of Kaposi's sarcoma? Simonart, Thierry BMC Cancer Debate BACKGROUND: Kaposi's sarcoma (KS) is a mesenchymal tumour associated with human herpesvirus-8 infection. However, the incidence of human herpesvirus-8 infection is far higher than the prevalence of KS, suggesting that viral infection per se is not sufficient for the development of malignancy and that one or more additional cofactors are required. DISCUSSION: Epidemiological data suggest that iron may be one of the cofactors involved in the pathogenesis of KS. Iron is a well-known carcinogen and may favour KS growth through several pathways. Based on the apoptotic and antiproliferative effect of iron chelation on KS cells, it is suggested that iron withdrawal strategies could be developed for the management of KS. Studies using potent iron chelators in suitable KS animal models are critical to evaluate whether iron deprivation may be a useful anti-KS strategy. SUMMARY: It is suggested that iron may be one of non-viral co-factors involved of KS pathogenesis and that iron withdrawal strategies might interfere with tumour growth in patients with KS. BioMed Central 2004-01-15 /pmc/articles/PMC317471/ /pubmed/14725718 http://dx.doi.org/10.1186/1471-2407-4-1 Text en Copyright © 2004 Simonart; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Debate
Simonart, Thierry
Iron: a target for the management of Kaposi's sarcoma?
title Iron: a target for the management of Kaposi's sarcoma?
title_full Iron: a target for the management of Kaposi's sarcoma?
title_fullStr Iron: a target for the management of Kaposi's sarcoma?
title_full_unstemmed Iron: a target for the management of Kaposi's sarcoma?
title_short Iron: a target for the management of Kaposi's sarcoma?
title_sort iron: a target for the management of kaposi's sarcoma?
topic Debate
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC317471/
https://www.ncbi.nlm.nih.gov/pubmed/14725718
http://dx.doi.org/10.1186/1471-2407-4-1
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