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Epigenome-wide association study of lung cancer among never smokers in two prospective cohorts in Shanghai, China.
Rahman, Mohammad L; Breeze, Charles E; Shu, Xiao-Ou; Wong, Jason Y Y; Blechter, Batel; Cardenas, Andres; Wang, Xuting; Ji, Bu-Tian; Hu, Wei; Cai, Qiuyin; Hosgood, H Dean; Yang, Gong; Shi, Jianxin; Long, Jirong; Gao, Yu-Tang; Bell, Douglas A; Zheng, Wei; Rothman, Nathaniel; Lan, Qing.
Afiliación
  • Rahman ML; Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland, USA mohammad.rahman2@nih.gov.
  • Breeze CE; Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland, USA.
  • Shu XO; Vanderbilt University Medical Center, Nashville, Tennessee, USA.
  • Wong JYY; Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland, USA.
  • Blechter B; Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland, USA.
  • Cardenas A; Department of Epidemiology and Population Health, Stanford University, Stanford, California, USA.
  • Wang X; Immunity, Inflammation and Diseases Laboratory, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina, USA.
  • Ji BT; Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland, USA.
  • Hu W; Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland, USA.
  • Cai Q; Vanderbilt University, Nashville, Tennessee, USA.
  • Hosgood HD; Albert Einstein College of Medicine, Bronx, New York, USA.
  • Yang G; Department of Medicine, Vanderbilt-Ingram Cancer Center, Nashville, Tennessee, USA.
  • Shi J; Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland, USA.
  • Long J; Department of Medicine, Vanderbilt-Ingram Cancer Center, Nashville, Tennessee, USA.
  • Gao YT; Shanghai Cancer Institute, Shanghai, China.
  • Bell DA; Immunity, Inflammation and Diseases Laboratory, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina, USA.
  • Zheng W; Vanderbilt University Medical Center, Nashville, Tennessee, USA.
  • Rothman N; Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland, USA.
  • Lan Q; Division of Cancer Epidemiology and Genetics, National Cancer Institute, Rockville, Maryland, USA.
Thorax ; 79(8): 735-744, 2024 Jul 16.
Article en En | MEDLINE | ID: mdl-38702190
ABSTRACT

BACKGROUND:

The aetiology of lung cancer among individuals who never smoked remains elusive, despite 15% of lung cancer cases in men and 53% in women worldwide being unrelated to smoking. Epigenetic alterations, particularly DNA methylation (DNAm) changes, have emerged as potential drivers. Yet, few prospective epigenome-wide association studies (EWAS), primarily focusing on peripheral blood DNAm with limited representation of never smokers, have been conducted.

METHODS:

We conducted a nested case-control study of 80 never-smoking incident lung cancer cases and 83 never-smoking controls within the Shanghai Women's Health Study and Shanghai Men's Health Study. DNAm was measured in prediagnostic oral rinse samples using Illumina MethylationEPIC array. Initially, we conducted an EWAS to identify differentially methylated positions (DMPs) associated with lung cancer in the discovery sample of 101 subjects. The top 50 DMPs were further evaluated in a replication sample of 62 subjects, and results were pooled using fixed-effect meta-analysis.

RESULTS:

Our study identified three DMPs significantly associated with lung cancer at the epigenome-wide significance level of p<8.22×10-8. These DMPs were identified as cg09198866 (MYH9; TXN2), cg01411366 (SLC9A10) and cg12787323. Furthermore, examination of the top 1000 DMPs indicated significant enrichment in epithelial regulatory regions and their involvement in small GTPase-mediated signal transduction pathways. Additionally, GrimAge acceleration was identified as a risk factor for lung cancer (OR=1.19 per year; 95% CI 1.06 to 1.34).

CONCLUSIONS:

While replication in a larger sample size is necessary, our findings suggest that DNAm patterns in prediagnostic oral rinse samples could provide novel insights into the underlying mechanisms of lung cancer in never smokers.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Metilación de ADN / Estudio de Asociación del Genoma Completo / Epigenoma / Neoplasias Pulmonares País/Región como asunto: Asia Idioma: En Revista: Thorax Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Metilación de ADN / Estudio de Asociación del Genoma Completo / Epigenoma / Neoplasias Pulmonares País/Región como asunto: Asia Idioma: En Revista: Thorax Año: 2024 Tipo del documento: Article