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本文引用的文献

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Chronic exposure to estrogen and the tobacco carcinogen NNK cooperatively modulates nicotinic receptors in small airway epithelial cells.慢性暴露于雌激素和烟草致癌物 NNK 可协同调节小气道上皮细胞中的烟碱型乙酰胆碱受体。
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A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma.一项肺癌全基因组关联研究确定了5号染色体p15区域与腺癌风险相关。
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Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study.解析常见基因变异对肺癌风险的影响:一项全基因组关联研究。
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Genome-wide analysis of survival in early-stage non-small-cell lung cancer.早期非小细胞肺癌生存情况的全基因组分析。
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Chronic obstructive lung diseases and risk of non-small cell lung cancer in women.慢性阻塞性肺疾病与女性非小细胞肺癌风险
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Tobacco and estrogen metabolic polymorphisms and risk of non-small cell lung cancer in women.烟草与雌激素代谢多态性及女性非小细胞肺癌风险
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Common 5p15.33 and 6p21.33 variants influence lung cancer risk.常见的5p15.33和6p21.33变异影响肺癌风险。
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10
Gamma-aminobutyric acid receptor genes and nicotine dependence: evidence for association from a case-control study.γ-氨基丁酸受体基因与尼古丁依赖:一项病例对照研究的关联证据
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1812 名非裔美国人肺癌的混合映射分析。

Admixture mapping of lung cancer in 1812 African-Americans.

机构信息

Karmanos Cancer Institute, Detroit, MI 48201, USA.

出版信息

Carcinogenesis. 2011 Mar;32(3):312-7. doi: 10.1093/carcin/bgq252. Epub 2010 Nov 29.

DOI:10.1093/carcin/bgq252
PMID:21115650
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3047238/
Abstract

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.

摘要

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。