Investigating causal relationship among inflammatory cytokines and oropharyngeal cancer: Mendelian randomization

Abstract Objectives This study aims to use Mendelian randomisation to identify the causal relationship between a spectrum of 41 inflammatory cytokines and the development of oropharyngeal cancer. Methods This study investigated genetic variants that have been associated with oral and oropharyngeal c...

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Main Authors: Sibo Xu, Yiguo Li, Wei Chen, Ke Wang
Format: Article
Language:English
Published: Springer 2025-01-01
Series:Discover Oncology
Subjects:
Online Access:https://doi.org/10.1007/s12672-025-01809-8
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author Sibo Xu
Yiguo Li
Wei Chen
Ke Wang
author_facet Sibo Xu
Yiguo Li
Wei Chen
Ke Wang
author_sort Sibo Xu
collection DOAJ
description Abstract Objectives This study aims to use Mendelian randomisation to identify the causal relationship between a spectrum of 41 inflammatory cytokines and the development of oropharyngeal cancer. Methods This study investigated genetic variants that have been associated with oral and oropharyngeal cancer using data from a large GWAS. Inflammatory cytokine data were obtained from 8293 asymptomatic individuals. The study primarily used inverse variance weighted and MR-Egger methods to determine the causal relationship between inflammatory cytokines and cancer incidence, complemented by a series of sensitivity analyses including MR-Egger, simple mode, weighted mode, weighted median and leave-one-out approaches. Results Our study demonstrates that higher levels of interleukin-7 (IL-7) and interleukin-5 (IL-5) slightly increase the odds of oropharyngeal cancer by 0.07% [OR: 1.0007, p = 0.005] and 0.04% [OR: 1.0004, p = 0.015], corresponding to a modest increase. Similarly, increased PDGF-bb and CTACK levels are modestly associated with increased odds of oral and oropharyngeal cancer by 0.22% [OR: 1.0022, p = 0.031] and 0.17% [OR: 1.0017, p = 0.043], respectively. Conclusion This investigation posits that IL-5 and IL-7 may be pertinent factors in the etiology of Oropharyngeal cancer, while PDGF bb and CTACK are likely implicated in the pathogenesis of both oral and oropharyngeal cancers.
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spelling doaj-art-3ac9047304e04ece8b8ef96bd1f8e5422025-02-02T12:30:28ZengSpringerDiscover Oncology2730-60112025-01-0116111010.1007/s12672-025-01809-8Investigating causal relationship among inflammatory cytokines and oropharyngeal cancer: Mendelian randomizationSibo Xu0Yiguo Li1Wei Chen2Ke Wang3Department of Stomatology, Hangzhou Linping District First People’s HospitalDepartment of Stomatology, Hangzhou Linping District First People’s HospitalDepartment of Stomatology, Hangzhou Linping District First People’s HospitalDepartment of Stomatology, Hangzhou Linping District First People’s HospitalAbstract Objectives This study aims to use Mendelian randomisation to identify the causal relationship between a spectrum of 41 inflammatory cytokines and the development of oropharyngeal cancer. Methods This study investigated genetic variants that have been associated with oral and oropharyngeal cancer using data from a large GWAS. Inflammatory cytokine data were obtained from 8293 asymptomatic individuals. The study primarily used inverse variance weighted and MR-Egger methods to determine the causal relationship between inflammatory cytokines and cancer incidence, complemented by a series of sensitivity analyses including MR-Egger, simple mode, weighted mode, weighted median and leave-one-out approaches. Results Our study demonstrates that higher levels of interleukin-7 (IL-7) and interleukin-5 (IL-5) slightly increase the odds of oropharyngeal cancer by 0.07% [OR: 1.0007, p = 0.005] and 0.04% [OR: 1.0004, p = 0.015], corresponding to a modest increase. Similarly, increased PDGF-bb and CTACK levels are modestly associated with increased odds of oral and oropharyngeal cancer by 0.22% [OR: 1.0022, p = 0.031] and 0.17% [OR: 1.0017, p = 0.043], respectively. Conclusion This investigation posits that IL-5 and IL-7 may be pertinent factors in the etiology of Oropharyngeal cancer, while PDGF bb and CTACK are likely implicated in the pathogenesis of both oral and oropharyngeal cancers.https://doi.org/10.1007/s12672-025-01809-8Oropharyngeal cancerBiomarkersMendelian randomizationGenome-wide association studies (GWAS)Inflammatory cytokines
spellingShingle Sibo Xu
Yiguo Li
Wei Chen
Ke Wang
Investigating causal relationship among inflammatory cytokines and oropharyngeal cancer: Mendelian randomization
Discover Oncology
Oropharyngeal cancer
Biomarkers
Mendelian randomization
Genome-wide association studies (GWAS)
Inflammatory cytokines
title Investigating causal relationship among inflammatory cytokines and oropharyngeal cancer: Mendelian randomization
title_full Investigating causal relationship among inflammatory cytokines and oropharyngeal cancer: Mendelian randomization
title_fullStr Investigating causal relationship among inflammatory cytokines and oropharyngeal cancer: Mendelian randomization
title_full_unstemmed Investigating causal relationship among inflammatory cytokines and oropharyngeal cancer: Mendelian randomization
title_short Investigating causal relationship among inflammatory cytokines and oropharyngeal cancer: Mendelian randomization
title_sort investigating causal relationship among inflammatory cytokines and oropharyngeal cancer mendelian randomization
topic Oropharyngeal cancer
Biomarkers
Mendelian randomization
Genome-wide association studies (GWAS)
Inflammatory cytokines
url https://doi.org/10.1007/s12672-025-01809-8
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