Lee Truelian, George Christopher D, Jiang Chen, Asgari Maryam M, Nijsten Tamar, Pardo Luba M, Choquet Hélène
Harvard Medical School, Boston, Massachusetts.
Department of Dermatology, Erasmus MC Cancer Institute, University Medical Center Rotterdam, Rotterdam, Netherlands.
JAAD Int. 2023 Dec 3;14:69-76. doi: 10.1016/j.jdin.2023.11.005. eCollection 2024 Mar.
BACKGROUND/PURPOSE: Cutaneous squamous cell carcinoma (cSCC) is one of the most common malignancies worldwide. While several environmental risk factors for cSCC are well established, there is conflicting evidence on cigarette smoking (and its potential causal effect) and cSCC risk. Furthermore, it is unclear if these potential associations represent causal, modifiable risk factors for cSCC development. This study aims to assess the nature of the associations between cigarette smoking traits (smoking initiation, amount smoked, and lifetime smoking exposure) and cSCC risk using two-sample Mendelian randomization analyses.
Genetic instruments, based on common genetic variants associated with cigarette smoking traits ( < 5 × 10), were derived from published genome-wide association studies (GWASs). For cSCC, we used GWAS summary statistics from the Kaiser Permanente GERA cohort (7701 cSCC cases and 60,167 controls; all non-Hispanic Whites).
We found modest evidence that genetically determined lifetime smoking was associated with cSCC (inverse-variance weighted method: OR[95% CI] = 1.47[1.09-1.98]; = .012), suggesting it may be a causal risk factor for cSCC. We did not detect any evidence of association between genetically determined smoking initiation or amount smoked and cSCC risk.
Study findings highlight the importance of smoking prevention and may support risk-stratified cSCC screening strategies based on carcinogen exposure and other genetic and clinical information.
背景/目的:皮肤鳞状细胞癌(cSCC)是全球最常见的恶性肿瘤之一。虽然已明确cSCC的几种环境风险因素,但关于吸烟(及其潜在因果效应)与cSCC风险的证据存在冲突。此外,尚不清楚这些潜在关联是否代表cSCC发生的因果性、可改变的风险因素。本研究旨在通过两样本孟德尔随机化分析评估吸烟特征(开始吸烟、吸烟量和终生吸烟暴露量)与cSCC风险之间关联的性质。
基于与吸烟特征相关的常见基因变异(<5×10)构建的基因工具,来源于已发表的全基因组关联研究(GWAS)。对于cSCC,我们使用了凯撒永久医疗集团GERA队列的GWAS汇总统计数据(7701例cSCC病例和60167例对照;均为非西班牙裔白人)。
我们发现适度的证据表明,基因决定的终生吸烟与cSCC相关(逆方差加权法:OR[95%CI]=1.47[1.09 - 1.98];=0.012),表明它可能是cSCC的一个因果风险因素。我们未检测到基因决定的开始吸烟或吸烟量与cSCC风险之间存在关联的任何证据。
研究结果突出了吸烟预防的重要性,并可能支持基于致癌物暴露以及其他基因和临床信息的cSCC风险分层筛查策略。