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Unveiling the Association between HPV and Pan-Cancers: A Bidirectional Two-Sample Mendelian Randomization Study

SIMPLE SUMMARY: The association between HPV and cancer has been the focus of research, but there has been a lack of a comprehensive high-level evidence studies to systematically examine the relationship between them. Using Mendelian randomization, this paper provided an extensive analysis of the cau...

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Autores principales: Sun, Jianxuan, Xiang, Jiacheng, An, Ye, Xu, Jinzhou, Xiong, Yifan, Wang, Shaogang, Xia, Qidong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10650873/
https://www.ncbi.nlm.nih.gov/pubmed/37958321
http://dx.doi.org/10.3390/cancers15215147
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author Sun, Jianxuan
Xiang, Jiacheng
An, Ye
Xu, Jinzhou
Xiong, Yifan
Wang, Shaogang
Xia, Qidong
author_facet Sun, Jianxuan
Xiang, Jiacheng
An, Ye
Xu, Jinzhou
Xiong, Yifan
Wang, Shaogang
Xia, Qidong
author_sort Sun, Jianxuan
collection PubMed
description SIMPLE SUMMARY: The association between HPV and cancer has been the focus of research, but there has been a lack of a comprehensive high-level evidence studies to systematically examine the relationship between them. Using Mendelian randomization, this paper provided an extensive analysis of the causal effect of HPV in cancer development. Our study conclusively identified HPV16 as a risk factor implicated in the development of bladder cancer, colorectal cancer, and breast cancer, while HPV18 was identified as a risk factor for prostate cancer, ovarian cancer, lung cancer and breast cancer. The results of Mendelian randomization also showed that HPV16 may be a protective factor for prostate cancer, anal cancer, lung cancer and oropharyngeal cancer, while HPV18 may be a protective factor for vaginal cancer. ABSTRACT: Introduction: More and more studies have focused on the associations between human papillomavirus (HPV) infection and pan-cancers. However, current evidence is largely based on retrospective studies, which are susceptible to confounding factors and do not enable the establishment of causal relationships. Methods: A bidirectional two-sample Mendelian randomization (MR) design was employed to thoroughly evaluate the causal relationships between HPV and 12 site-specific cancers except cervical cancer. Single nucleoside polymers (SNPs) with strong evidence from genome-wide association studies (GWAS) were selected from HPV exposure datasets and used as instrumental variables (IVs) in this study. For the MR analysis results, MR-Egger’s intercept P test, MR-PRESSO global test, Cochran’s Q test and a leave-one-out test were applied for sensitivity analysis. Using HPVTIMER, we also performed immune infiltration analyses in head and neck squamous cell carcinoma (HNSCC), oropharyngeal squamous cell carcinoma (OPSCC) and vulval squamous cell carcinoma (VSCC) to evaluate the tumor-immune microenvironment. Results: Based on the evidence of MR analysis, our study conclusively identified HPV16 as a risk factor implicated in the development of bladder cancer, colorectal cancer, and breast cancer, while HPV18 was identified as a risk factor for prostate cancer, ovarian cancer, lung cancer and breast cancer. The MR results also showed that HPV16 may be a protective factor for prostate cancer, anal cancer, lung cancer and oropharyngeal cancer, while HPV18 may be a protective factor for vaginal cancer. Conclusion: An HPV infection may modulate the immune microenvironment and therefore has a potential inhibitory effect on the development of certain cancers. These conclusions provided new insights into the potential mechanisms of carcinogenesis and needed further research for validation.
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spelling pubmed-106508732023-10-26 Unveiling the Association between HPV and Pan-Cancers: A Bidirectional Two-Sample Mendelian Randomization Study Sun, Jianxuan Xiang, Jiacheng An, Ye Xu, Jinzhou Xiong, Yifan Wang, Shaogang Xia, Qidong Cancers (Basel) Article SIMPLE SUMMARY: The association between HPV and cancer has been the focus of research, but there has been a lack of a comprehensive high-level evidence studies to systematically examine the relationship between them. Using Mendelian randomization, this paper provided an extensive analysis of the causal effect of HPV in cancer development. Our study conclusively identified HPV16 as a risk factor implicated in the development of bladder cancer, colorectal cancer, and breast cancer, while HPV18 was identified as a risk factor for prostate cancer, ovarian cancer, lung cancer and breast cancer. The results of Mendelian randomization also showed that HPV16 may be a protective factor for prostate cancer, anal cancer, lung cancer and oropharyngeal cancer, while HPV18 may be a protective factor for vaginal cancer. ABSTRACT: Introduction: More and more studies have focused on the associations between human papillomavirus (HPV) infection and pan-cancers. However, current evidence is largely based on retrospective studies, which are susceptible to confounding factors and do not enable the establishment of causal relationships. Methods: A bidirectional two-sample Mendelian randomization (MR) design was employed to thoroughly evaluate the causal relationships between HPV and 12 site-specific cancers except cervical cancer. Single nucleoside polymers (SNPs) with strong evidence from genome-wide association studies (GWAS) were selected from HPV exposure datasets and used as instrumental variables (IVs) in this study. For the MR analysis results, MR-Egger’s intercept P test, MR-PRESSO global test, Cochran’s Q test and a leave-one-out test were applied for sensitivity analysis. Using HPVTIMER, we also performed immune infiltration analyses in head and neck squamous cell carcinoma (HNSCC), oropharyngeal squamous cell carcinoma (OPSCC) and vulval squamous cell carcinoma (VSCC) to evaluate the tumor-immune microenvironment. Results: Based on the evidence of MR analysis, our study conclusively identified HPV16 as a risk factor implicated in the development of bladder cancer, colorectal cancer, and breast cancer, while HPV18 was identified as a risk factor for prostate cancer, ovarian cancer, lung cancer and breast cancer. The MR results also showed that HPV16 may be a protective factor for prostate cancer, anal cancer, lung cancer and oropharyngeal cancer, while HPV18 may be a protective factor for vaginal cancer. Conclusion: An HPV infection may modulate the immune microenvironment and therefore has a potential inhibitory effect on the development of certain cancers. These conclusions provided new insights into the potential mechanisms of carcinogenesis and needed further research for validation. MDPI 2023-10-26 /pmc/articles/PMC10650873/ /pubmed/37958321 http://dx.doi.org/10.3390/cancers15215147 Text en © 2023 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 Article
Sun, Jianxuan
Xiang, Jiacheng
An, Ye
Xu, Jinzhou
Xiong, Yifan
Wang, Shaogang
Xia, Qidong
Unveiling the Association between HPV and Pan-Cancers: A Bidirectional Two-Sample Mendelian Randomization Study
title Unveiling the Association between HPV and Pan-Cancers: A Bidirectional Two-Sample Mendelian Randomization Study
title_full Unveiling the Association between HPV and Pan-Cancers: A Bidirectional Two-Sample Mendelian Randomization Study
title_fullStr Unveiling the Association between HPV and Pan-Cancers: A Bidirectional Two-Sample Mendelian Randomization Study
title_full_unstemmed Unveiling the Association between HPV and Pan-Cancers: A Bidirectional Two-Sample Mendelian Randomization Study
title_short Unveiling the Association between HPV and Pan-Cancers: A Bidirectional Two-Sample Mendelian Randomization Study
title_sort unveiling the association between hpv and pan-cancers: a bidirectional two-sample mendelian randomization study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10650873/
https://www.ncbi.nlm.nih.gov/pubmed/37958321
http://dx.doi.org/10.3390/cancers15215147
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