Tsai Ya-Yu, McGlynn Katherine A, Hu Ying, Cassidy Anna B, Arnold John, Engstrom Paul F, Buetow Kenneth H
Laboratory of Population Genetics, Center for Cancer Research, National Cancer Institute, NIH, DHHS, Bethesda, MD, USA.
Lung Cancer. 2003 Sep;41(3):269-81. doi: 10.1016/s0169-5002(03)00238-1.
Cigarette smoking is the dominant risk factor for lung cancer, but only a minority of smokers ever develops tumors. Though genetic susceptibility is likely to explain some of the variability in risk, results from previous studies of genetic polymorphisms have been inconclusive. As diet may also affect the risk of lung cancer, it is possible that the degree of risk produced by smoking and genetic susceptibility varies, depending on diet. To assess this hypothesis, we conducted a case-control study to examine the effect of cigarette smoking, dietary patterns and variation in genes involved in phase II metabolism. A total of 254 individuals with lung cancer and 184 healthy controls were recruited for the study. To identify persons with similar dietary patterns, cluster analysis was performed using nutrient densities of four major dietary constituents: protein, carbohydrate, animal fat, and dietary fiber. Two groups of individuals were identified with distinct dietary patterns: (1) a group (n=241) with a high intake of animal fat and protein and a low intake of carbohydrates and dietary fiber (the 'unhealthy' pattern) and (2) a group (n=197) with a high intake of fiber and carbohydrate and a low intake of protein and animal fat (the 'healthy' pattern) [corrected]. On stratified analysis, several genotype/dietary pattern combinations were found to affect risk of lung cancer. Smokers who were not homozygous for the most common GSTP1 allele and had a healthy dietary pattern were at significantly lower risk than smokers who were homozygous for the GSTP1 common allele and who had an unhealthy dietary pattern (OR=0.16, 95%CI: 0.04-0.57). Among smokers who were GSTM1 null, persons with a healthy dietary pattern were at lower risk than persons with an unhealthy dietary pattern (OR: 0.46, 95%CI: 0.21-1.01). Among smokers with an unhealthy dietary patterns, persons with a His/His genotype in the exon 3 polymorphism of EPHX1 were at significantly lower risk that persons who were not homozygous. These data suggest that dietary factors may affect the risk imposed by genetic susceptibility at detoxification loci. Adjustments using dietary pattern may be useful in elucidating the effects of polymorphisms in genes responsible for carcinogen metabolism.
吸烟是肺癌的主要危险因素,但只有少数吸烟者会患上肿瘤。虽然遗传易感性可能解释了部分风险差异,但先前关于基因多态性的研究结果尚无定论。由于饮食也可能影响肺癌风险,因此吸烟和遗传易感性所产生的风险程度可能因饮食而异。为了评估这一假设,我们开展了一项病例对照研究,以检验吸烟、饮食模式以及参与Ⅱ期代谢的基因变异的影响。该研究共招募了254名肺癌患者和184名健康对照者。为了识别饮食模式相似的人群,利用四种主要饮食成分(蛋白质、碳水化合物、动物脂肪和膳食纤维)的营养密度进行聚类分析。确定了两组饮食模式不同的人群:(1)一组(n = 241)动物脂肪和蛋白质摄入量高,碳水化合物和膳食纤维摄入量低(“不健康”模式);(2)一组(n = 197)膳食纤维和碳水化合物摄入量高,蛋白质和动物脂肪摄入量低(“健康”模式)[已校正]。分层分析发现,几种基因型/饮食模式组合会影响肺癌风险。对于最常见的GSTP1等位基因并非纯合子且饮食模式健康的吸烟者,其患癌风险显著低于GSTP1常见等位基因纯合子且饮食模式不健康的吸烟者(比值比=0.16,95%置信区间:0.04 - 0.57)。在GSTM1基因缺失的吸烟者中,饮食模式健康者的风险低于饮食模式不健康者(比值比:0.46,95%置信区间:0.21 - 1.01)。在饮食模式不健康的吸烟者中,EPHX1外显子3多态性为His/His基因型者的风险显著低于非纯合子者。这些数据表明,饮食因素可能影响解毒位点遗传易感性所带来的风险。利用饮食模式进行调整可能有助于阐明负责致癌物代谢的基因多态性的影响。