Karmanos Cancer Institute, Detroit, MI 48201, USA.
Carcinogenesis. 2011 Mar;32(3):312-7. doi: 10.1093/carcin/bgq252. Epub 2010 Nov 29.
Lung cancer continues to be the leading cause of cancer death in the USA and the best example of a cancer with undisputed evidence of environmental risk. However, a genetic contribution to lung cancer has also been demonstrated by studies of familial aggregation, family-based linkage, candidate gene studies and most recently genome-wide association studies (GWAS). The African-American population has been underrepresented in these genetic studies and has patterns of cigarette use and linkage disequilibrium that differ from patterns in other populations. Therefore, studies in African-Americans can provide complementary data to localize lung cancer susceptibility genes and explore smoking dependence-related genes. We used admixture mapping to further characterize genetic risk of lung cancer in a series of 837 African-American lung cancer cases and 975 African-American controls genotyped at 1344 ancestry informative single-nucleotide polymorphisms. Both case-only and case-control analyses were conducted using ADMIXMAP adjusted for age, sex, pack-years of smoking, family history of lung cancer, history of emphysema and study site. In case-only analyses, excess European ancestry was observed over a wide region on chromosome 1 with the largest excess seen at rs6587361 for non-small-cell lung cancer (NSCLC) (Z-score = -4.33; P = 1.5 × 10⁻⁵) and for women with NSCLC (Z-score = -4.82; P = 1.4 × 10⁻⁶). Excess African ancestry was also observed on chromosome 3q with a peak Z-score of 3.33 (P = 0.0009) at rs181696 among ever smokers with NSCLC. These results add to the findings from the GWAS in Caucasian populations and suggest novel regions of interest.
肺癌仍然是美国癌症死亡的主要原因,也是最明显的环境风险致癌因素的范例。然而,家族聚集、基于家族的连锁、候选基因研究以及最近的全基因组关联研究(GWAS)已经证明肺癌存在遗传贡献。这些遗传研究中代表性不足的是非洲裔美国人,他们的吸烟习惯和连锁不平衡模式与其他人群不同。因此,在非裔美国人中进行研究可以提供补充数据,以定位肺癌易感性基因,并探索与吸烟依赖相关的基因。我们使用混合映射方法,对一系列 837 例非裔美国肺癌病例和 975 例非裔美国对照进行了基因分析,这些对照在 1344 个遗传信息单核苷酸多态性上进行了基因分型。使用 ADMIXMAP 进行病例仅分析和病例对照分析,该方法针对年龄、性别、吸烟包年数、肺癌家族史、肺气肿史和研究地点进行了调整。在病例仅分析中,在染色体 1 上观察到大量欧洲血统的多余,在非小细胞肺癌(NSCLC)的 rs6587361 处观察到最大的多余(Z 分数=-4.33;P=1.5×10⁻⁵),在非小细胞肺癌的女性中观察到最大的多余(Z 分数=-4.82;P=1.4×10⁻⁶)。在 rs181696 处,在 3q 染色体上也观察到了非洲血统的多余,在有 NSCLC 的曾经吸烟者中,峰值 Z 分数为 3.33(P=0.0009)。这些结果增加了在白种人群中进行的 GWAS 的发现,并提出了新的感兴趣区域。