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Diabetes and risk of Kaposi's sarcoma: effects of high glucose on reactivation and infection of Kaposi's sarcoma-associated herpesvirus

Patients with diabetes are generally prone to pathogen infection and tumor progression. Here, we investigated the potential association between diabetes and Kaposi's sarcoma (KS), a tumor linked to infection with Kaposi's sarcoma-associated herpesvirus (KSHV). By using Taiwan's Nation...

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Autores principales: Chang, Pey-Jium, Yang, Yao-Hsu, Chen, Pau-Chung, Chen, Lee-Wen, Wang, Shie-Shan, Shih, Ying-Ju, Chen, Li-Yu, Chen, Chi-Jen, Hung, Chien-Hui, Lin, Chun-Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5655223/
https://www.ncbi.nlm.nih.gov/pubmed/29113328
http://dx.doi.org/10.18632/oncotarget.19685
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author Chang, Pey-Jium
Yang, Yao-Hsu
Chen, Pau-Chung
Chen, Lee-Wen
Wang, Shie-Shan
Shih, Ying-Ju
Chen, Li-Yu
Chen, Chi-Jen
Hung, Chien-Hui
Lin, Chun-Liang
author_facet Chang, Pey-Jium
Yang, Yao-Hsu
Chen, Pau-Chung
Chen, Lee-Wen
Wang, Shie-Shan
Shih, Ying-Ju
Chen, Li-Yu
Chen, Chi-Jen
Hung, Chien-Hui
Lin, Chun-Liang
author_sort Chang, Pey-Jium
collection PubMed
description Patients with diabetes are generally prone to pathogen infection and tumor progression. Here, we investigated the potential association between diabetes and Kaposi's sarcoma (KS), a tumor linked to infection with Kaposi's sarcoma-associated herpesvirus (KSHV). By using Taiwan's National Health Insurance Research Database, we found that diabetes is statistically associated with increased risk of KS in a case-control study. Since a high level of blood sugar is the hallmark of diabetes, we determined whether high glucose promotes both KSHV reactivation and infection, which are crucial for KS pathogenesis. Our results showed that high glucose significantly increases lytic reactivation of KSHV but not Epstein-Barr virus, another related human oncogenic gammaherpesvirus, in latently infected cells. Activation of the transcription factor AP1 by high glucose is critically required for the onset of KSHV lytic reactivation. We also demonstrated that high glucose enhances susceptibility of various target cells to KSHV infection. Particularly, in endothelial and epithelial cells, levels of specific cellular receptors for KSHV entry, including integrin α3β1 and xCT/CD98, are elevated under high glucose conditions, which correlate with the enhanced cell susceptibility to infection. Taken together, our studies implicate that the high-glucose microenvironment may be an important predisposing factor for KS development.
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spelling pubmed-56552232017-11-06 Diabetes and risk of Kaposi's sarcoma: effects of high glucose on reactivation and infection of Kaposi's sarcoma-associated herpesvirus Chang, Pey-Jium Yang, Yao-Hsu Chen, Pau-Chung Chen, Lee-Wen Wang, Shie-Shan Shih, Ying-Ju Chen, Li-Yu Chen, Chi-Jen Hung, Chien-Hui Lin, Chun-Liang Oncotarget Research Paper Patients with diabetes are generally prone to pathogen infection and tumor progression. Here, we investigated the potential association between diabetes and Kaposi's sarcoma (KS), a tumor linked to infection with Kaposi's sarcoma-associated herpesvirus (KSHV). By using Taiwan's National Health Insurance Research Database, we found that diabetes is statistically associated with increased risk of KS in a case-control study. Since a high level of blood sugar is the hallmark of diabetes, we determined whether high glucose promotes both KSHV reactivation and infection, which are crucial for KS pathogenesis. Our results showed that high glucose significantly increases lytic reactivation of KSHV but not Epstein-Barr virus, another related human oncogenic gammaherpesvirus, in latently infected cells. Activation of the transcription factor AP1 by high glucose is critically required for the onset of KSHV lytic reactivation. We also demonstrated that high glucose enhances susceptibility of various target cells to KSHV infection. Particularly, in endothelial and epithelial cells, levels of specific cellular receptors for KSHV entry, including integrin α3β1 and xCT/CD98, are elevated under high glucose conditions, which correlate with the enhanced cell susceptibility to infection. Taken together, our studies implicate that the high-glucose microenvironment may be an important predisposing factor for KS development. Impact Journals LLC 2017-07-28 /pmc/articles/PMC5655223/ /pubmed/29113328 http://dx.doi.org/10.18632/oncotarget.19685 Text en Copyright: © 2017 Chang et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Research Paper
Chang, Pey-Jium
Yang, Yao-Hsu
Chen, Pau-Chung
Chen, Lee-Wen
Wang, Shie-Shan
Shih, Ying-Ju
Chen, Li-Yu
Chen, Chi-Jen
Hung, Chien-Hui
Lin, Chun-Liang
Diabetes and risk of Kaposi's sarcoma: effects of high glucose on reactivation and infection of Kaposi's sarcoma-associated herpesvirus
title Diabetes and risk of Kaposi's sarcoma: effects of high glucose on reactivation and infection of Kaposi's sarcoma-associated herpesvirus
title_full Diabetes and risk of Kaposi's sarcoma: effects of high glucose on reactivation and infection of Kaposi's sarcoma-associated herpesvirus
title_fullStr Diabetes and risk of Kaposi's sarcoma: effects of high glucose on reactivation and infection of Kaposi's sarcoma-associated herpesvirus
title_full_unstemmed Diabetes and risk of Kaposi's sarcoma: effects of high glucose on reactivation and infection of Kaposi's sarcoma-associated herpesvirus
title_short Diabetes and risk of Kaposi's sarcoma: effects of high glucose on reactivation and infection of Kaposi's sarcoma-associated herpesvirus
title_sort diabetes and risk of kaposi's sarcoma: effects of high glucose on reactivation and infection of kaposi's sarcoma-associated herpesvirus
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5655223/
https://www.ncbi.nlm.nih.gov/pubmed/29113328
http://dx.doi.org/10.18632/oncotarget.19685
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