Evaluating the Effect of Telomere Length on Oral and Oropharyngeal Cancer Risk Using Mendelian Randomization

被引:0
作者
Lan, Li [1 ,2 ]
Zhang, Ruizhe [1 ]
Liang, Ya [1 ]
Chen, Huarong [1 ]
Zhao, Houyu [1 ]
Zhuo, Xianlu [1 ]
机构
[1] Guizhou Med Univ, Affiliated Hosp, Dept Otolaryngol, Guiyang 550004, Guizhou, Peoples R China
[2] Guizhou Prov Peoples Hosp, Hearing Ctr, Guiyang, Guizhou, Peoples R China
关键词
Telomere length; Oral and oropharyngeal cancer; Risk factors; Mendelian randomization; SQUAMOUS-CELL CARCINOMA; ASSOCIATION; HEAD; DYSFUNCTION; EXPRESSION; BIAS;
D O I
暂无
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Introduction: The aim of this study was to explore the causal relationship between telomere length and Oral and oropharyngeal cancers by using Mendelian randomization (MR) analysis. Methods: We carried out a 2-sample MR to examine the causal association between telomere length and Oral and oropharyngeal cancers. Two large genome-wide association studies (GWAS) were employed to identify single nucleotide polymorphisms (SNPs) as instrumental variables through statistical and biological approaches. The data on SNP-oral and oropharyngeal cancer risk factor associations were sourced from various consortia/UK Biobank. The inverse variance weighted (IVW) method was employed as the primary approach for overall causal estimation in MR, with sensitivity analyses conducted to assess potential confounding by pleiotropy, heterogeneity, and the leave-one-out analysis. Results: The statistically driven approach indicates limited evidence of a genetically causal effect of telomere length on the risk of oral cavity cancer (OR = 0.999, 95% CI 0.998-1.000, P = .100), oropharyngeal cancer (OR = 0.999, 95% CI 0.998-1.001, P = .650), combined oral and oropharyngeal cancer (OR = 0.999, 95% CI 0.998-1.000, P = .119) in Europeans. The biologically driven approach demonstrated consistent causal effects across all MR methods, thereby further strengthening the reliability of the results. Moreover, the MR-Egger (Q [df] 170.816 [130], P = .009) and inverse variance weighted methods (Q [df] 171.656 [131], P = .010) identified considerable heterogeneity among instrumental variable estimates in Oral cavity cancer, and no evidence of horizontal pleiotropy was detected. Conclusions: No significant causal associations between telomere length and Oral and oropharyngeal cancers were found in this study. (c) 2024 The Authors. Published by Elsevier Inc. on behalf of FDI World Dental Federation. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)
引用
收藏
页码:575 / 585
页数:11
相关论文
共 52 条
[1]   Telomere lengths in the oral epithelia with and without carcinoma [J].
Aida, Junko ;
Izumo, Toshiyuki ;
Shimomura, Naotaka ;
Nakamura, Ken-ichi ;
Ishikawa, Naoshi ;
Matsuura, Masaaki ;
Poon, Steven S. ;
Fujiwara, Mutsunori ;
Sawabe, Motoji ;
Arai, Tomio ;
Takubo, Kaiyo .
EUROPEAN JOURNAL OF CANCER, 2010, 46 (02) :430-438
[2]   Systematic analysis of telomere length and somatic alterations in 31 cancer types [J].
Barthel, Floris P. ;
Wei, Wei ;
Tang, Ming ;
Martinez-Ledesma, Emmanuel ;
Hu, Xin ;
Amin, Samirkumar B. ;
Akdemir, Kadir C. ;
Seth, Sahil ;
Song, Xingzhi ;
Wang, Qianghu ;
Lichtenberg, Tara ;
Hu, Jian ;
Zhang, Jianhua ;
Zheng, Siyuan ;
Verhaak, Roel G. W. .
NATURE GENETICS, 2017, 49 (03) :349-357
[3]   Exploratory Research Focusing on Oral Cancer Prevention: Challenges of Dealing With Informational and Cognitive Barriers [J].
Baumann, Eva ;
Scherer, Helmut ;
Link, Elena ;
Wiltfang, Joerg ;
Wenz, Hans-Juergen ;
Koller, Michael ;
Hertrampf, Katrin .
QUALITATIVE HEALTH RESEARCH, 2019, 29 (13) :1930-1941
[4]   Multiple cancer pathways regulate telomere protection [J].
Bejarano, Leire ;
Bosso, Giuseppe ;
Louzame, Jessica ;
Serrano, Rosa ;
Gomez-Casero, Elena ;
Martinez-Torrecuadrada, Jorge ;
Martinez, Sonia ;
Blanco-Aparicio, Carmen ;
Pastor, Joaquin ;
Blasco, Maria A. .
EMBO MOLECULAR MEDICINE, 2019, 11 (07)
[5]   The telomere proteins in tumorigenesis and clinical outcomes of oral squamous cell carcinoma [J].
Benhamou, Y. ;
Picco, V. ;
Pages, G. .
ORAL ONCOLOGY, 2016, 57 :46-53
[6]   Telomerase at the intersection of cancer and aging [J].
Bernardes de Jesus, Bruno ;
Blasco, Maria A. .
TRENDS IN GENETICS, 2013, 29 (09) :513-520
[7]   Extension of life-span by introduction of telomerase into normal human cells [J].
Bodnar, AG ;
Ouellette, M ;
Frolkis, M ;
Holt, SE ;
Chiu, CP ;
Morin, GB ;
Harley, CB ;
Shay, JW ;
Lichtsteiner, S ;
Wright, WE .
SCIENCE, 1998, 279 (5349) :349-352
[8]   Telomeres and telomerase in head and neck squamous cell carcinoma: from pathogenesis to clinical implications [J].
Boscolo-Rizzo, Paolo ;
Da Mosto, Maria Cristina ;
Rampazzo, Enrica ;
Giunco, Silvia ;
Del Mistro, Annarosa ;
Menegaldo, Anna ;
Baboci, Lorena ;
Mantovani, Monica ;
Tirelli, Giancarlo ;
De Rossi, Anita .
CANCER AND METASTASIS REVIEWS, 2016, 35 (03) :457-474
[9]  
Burgess Stephen, 2019, Wellcome Open Res, V4, P186, DOI 10.12688/wellcomeopenres.15555.3
[10]  
Burgess S, 2017, EUR J EPIDEMIOL, V32, P377, DOI 10.1007/s10654-017-0255-x