Kim Christopher, Bassig Bryan A, Seow Wei Jie, Hu Wei, Purdue Mark P, Shu Xiao-Ou, Huang Wen-Yi, Liu Chin-San, Cheng Wen-Ling, Lin Ta-Tsung, Xiang Yong-Bing, Ji Bu-Tian, Gao Yu-Tang, Chow Wong-Ho, Männistö Satu, Weinstein Stephanie J, Albanes Demetrius, Zheng Wei, Hosgood H Dean, Lim Unhee, Rothman Nathaniel, Lan Qing
Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
Vanderbilt University Medical Center, Nashville, Tennessee.
Cancer Epidemiol Biomarkers Prev. 2014 Dec;23(12):2977-80. doi: 10.1158/1055-9965.EPI-14-1070. Epub 2014 Oct 7.
We previously reported that higher levels of mitochondrial DNA copy number (mtDNA CN) were associated with lung cancer risk among male heavy smokers (i.e., ≥20 cigarettes per day) in the Alpha-Tocopherol Beta-Carotene (ATBC) study. Here, we present two additional prospective investigations nested in the Prostate, Lung, Colorectal, and Ovarian (PLCO) cancer screening trial and the Shanghai Women's Health Study (SWHS), and pooled with previously published data from ATBC.
All DNA were extracted from peripheral whole blood samples using the phenol-chloroform method, and mtDNA CN was assayed by fluorescence-based qPCR. Multivariate unconditional logistic regression models were used to estimate ORs and 95% confidence intervals for the association of mtDNA CN and lung cancer risk.
Overall, mtDNA CN was not associated with lung cancer risk in the PLCO, SWHS, or pooled populations (all P trends > 0.42, P heterogeneity = 0.0001), and mtDNA CN was inversely associated with lung cancer risk among male smokers in PLCO, the opposite direction observed in ATBC. In addition, the mtDNA CN association observed among male heavy smokers in ATBC was the opposite direction in PLCO.
mtDNA CN was not consistently associated with lung cancer risk across three prospective study populations from Europe, Asia, and the United States.
This pooled study suggests no consistent association between prediagnostic mtDNA CN levels and lung cancer risk across several populations. Cancer Epidemiol Biomarkers Prev; 23(12); 2977-80. ©2014 AACR.
我们之前在α-生育酚β-胡萝卜素(ATBC)研究中报告称,线粒体DNA拷贝数(mtDNA CN)水平较高与男性重度吸烟者(即每天≥20支香烟)的肺癌风险相关。在此,我们展示了另外两项前瞻性研究,它们嵌套于前列腺、肺癌、结直肠癌和卵巢癌(PLCO)筛查试验以及上海女性健康研究(SWHS)中,并与之前发表的ATBC数据合并。
所有DNA均采用酚-氯仿法从外周全血样本中提取,mtDNA CN通过基于荧光的定量PCR进行检测。多变量无条件逻辑回归模型用于估计mtDNA CN与肺癌风险关联的比值比(OR)和95%置信区间。
总体而言,在PLCO、SWHS或合并人群中,mtDNA CN与肺癌风险无关(所有P趋势>0.42,P异质性=0.0001),且在PLCO中,mtDNA CN与男性吸烟者的肺癌风险呈负相关,这与在ATBC中观察到的方向相反。此外,在ATBC中男性重度吸烟者中观察到的mtDNA CN关联在PLCO中方向相反。
在来自欧洲、亚洲和美国的三项前瞻性研究人群中,mtDNA CN与肺癌风险并非始终相关。
这项汇总研究表明,在多个人群中,诊断前mtDNA CN水平与肺癌风险之间不存在一致的关联。《癌症流行病学、生物标志物与预防》;23(12);2977 - 80。©2014美国癌症研究协会。