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Human herpesvirus 8 infection is associated with prostate cancer among IFNL4-ΔG carriers

BACKGROUND: The dinucleotide germline variant, rs368234815-ΔG, in the IFNL4 gene (IFNL4-ΔG) has been associated with prostate cancer among men at increased risk of sexually transmitted infections and reported to impair viral clearance. Human herpesvirus 8 (HHV-8) seropositivity has been associated w...

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Autores principales: Jenkins, Frank J., Minas, Tsion Z., Tang, Wei, Dorsey, Tiffany H., Ambs, Stefan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9592685/
https://www.ncbi.nlm.nih.gov/pubmed/35468990
http://dx.doi.org/10.1038/s41391-022-00546-1
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author Jenkins, Frank J.
Minas, Tsion Z.
Tang, Wei
Dorsey, Tiffany H.
Ambs, Stefan
author_facet Jenkins, Frank J.
Minas, Tsion Z.
Tang, Wei
Dorsey, Tiffany H.
Ambs, Stefan
author_sort Jenkins, Frank J.
collection PubMed
description BACKGROUND: The dinucleotide germline variant, rs368234815-ΔG, in the IFNL4 gene (IFNL4-ΔG) has been associated with prostate cancer among men at increased risk of sexually transmitted infections and reported to impair viral clearance. Human herpesvirus 8 (HHV-8) seropositivity has been associated with prostate cancer in Tobago. METHODS: We examined whether the association of HHV-8 with prostate cancer is IFNL4-ΔG-dependent among 728 IFNL4-ΔG-genotyped cases and 813 genotyped population-based controls from the NCI-Maryland Prostate Cancer Case-Control study. Associations between HHV-8 and prostate cancer were assessed in multivariable unconditional logistic regression models. We calculated adjusted odds ratios (OR) and stratified the analysis into men harboring the IFNL4-ΔG-variant and non-carriers (ΔG/ΔG or ΔG/TT vs. TT/TT). RESULTS: HHV-8 seropositivity was higher in cases than controls (11% vs. 6%) and this association was restricted to carriers of the ΔG allele (OR 2.19: 95% CI:1.38–3.48) in both African American (OR 1.96; 95% CI:1.08–3.56) and European American men (OR 2.59; 95% CI:1.20–5.56). CONCLUSIONS: HHV-8 seropositivity is associated with increased odds of prostate cancer in men harboring the IFNL4 rs368234815-ΔG variant. This study describes HHV-8 infection as a candidate prostate cancer risk factor in men with the IFNL4-ΔG genotype and supports the hypothesis that IFNL4-ΔG is a susceptibility factor that contributes to prostate cancer.
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spelling pubmed-95926852023-06-09 Human herpesvirus 8 infection is associated with prostate cancer among IFNL4-ΔG carriers Jenkins, Frank J. Minas, Tsion Z. Tang, Wei Dorsey, Tiffany H. Ambs, Stefan Prostate Cancer Prostatic Dis Article BACKGROUND: The dinucleotide germline variant, rs368234815-ΔG, in the IFNL4 gene (IFNL4-ΔG) has been associated with prostate cancer among men at increased risk of sexually transmitted infections and reported to impair viral clearance. Human herpesvirus 8 (HHV-8) seropositivity has been associated with prostate cancer in Tobago. METHODS: We examined whether the association of HHV-8 with prostate cancer is IFNL4-ΔG-dependent among 728 IFNL4-ΔG-genotyped cases and 813 genotyped population-based controls from the NCI-Maryland Prostate Cancer Case-Control study. Associations between HHV-8 and prostate cancer were assessed in multivariable unconditional logistic regression models. We calculated adjusted odds ratios (OR) and stratified the analysis into men harboring the IFNL4-ΔG-variant and non-carriers (ΔG/ΔG or ΔG/TT vs. TT/TT). RESULTS: HHV-8 seropositivity was higher in cases than controls (11% vs. 6%) and this association was restricted to carriers of the ΔG allele (OR 2.19: 95% CI:1.38–3.48) in both African American (OR 1.96; 95% CI:1.08–3.56) and European American men (OR 2.59; 95% CI:1.20–5.56). CONCLUSIONS: HHV-8 seropositivity is associated with increased odds of prostate cancer in men harboring the IFNL4 rs368234815-ΔG variant. This study describes HHV-8 infection as a candidate prostate cancer risk factor in men with the IFNL4-ΔG genotype and supports the hypothesis that IFNL4-ΔG is a susceptibility factor that contributes to prostate cancer. Nature Publishing Group UK 2022-04-25 2023 /pmc/articles/PMC9592685/ /pubmed/35468990 http://dx.doi.org/10.1038/s41391-022-00546-1 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit -http://creativecommons.org/licenses/by/4.0/. (https://creativecommons.org/licenses/by/4.0/)
spellingShingle Article
Jenkins, Frank J.
Minas, Tsion Z.
Tang, Wei
Dorsey, Tiffany H.
Ambs, Stefan
Human herpesvirus 8 infection is associated with prostate cancer among IFNL4-ΔG carriers
title Human herpesvirus 8 infection is associated with prostate cancer among IFNL4-ΔG carriers
title_full Human herpesvirus 8 infection is associated with prostate cancer among IFNL4-ΔG carriers
title_fullStr Human herpesvirus 8 infection is associated with prostate cancer among IFNL4-ΔG carriers
title_full_unstemmed Human herpesvirus 8 infection is associated with prostate cancer among IFNL4-ΔG carriers
title_short Human herpesvirus 8 infection is associated with prostate cancer among IFNL4-ΔG carriers
title_sort human herpesvirus 8 infection is associated with prostate cancer among ifnl4-δg carriers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9592685/
https://www.ncbi.nlm.nih.gov/pubmed/35468990
http://dx.doi.org/10.1038/s41391-022-00546-1
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