Genome-wide association study for lung cancer in 6531 African Americans reveals new susceptibility loci.

IF 3.1 2区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Jinyoung Byun, Younghun Han, Jiyeon Choi, Ryan Sun, Vikram R Shaw, Catherine Zhu, Xiangjun Xiao, Christine Lusk, Hoda Badr, Hyun-Sung Lee, Hee-Jin Jang, Yafang Li, Hyeyeun Lim, Erping Long, Yanhong Liu, Linda Kachuri, Kyle M Walsh, John K Wiencke, Demetrius Albanes, Stephen Lam, Adonina Tardon, Marian L Neuhouser, Matt J Barnett, Chu Chen, Stig Bojesen, Hermann Brenner, Maria Teresa Landi, Mattias Johansson, Angela Risch, H-Erich Wichmann, Heike Bickeböller, David C Christiani, Gad Rennert, Susanne Arnold, John K Field, Sanjay Shete, Loic Le Marchand, Geoffrey Liu, Angeline S Andrew, Shanbeh Zienolddiny, Kjell Grankvist, Mikael Johansson, Neil Caporaso, Fiona Taylor, Philip Lazarus, Matthew B Schabath, Melinda C Aldrich, Alpa Patel, Xihong Lin, Krista A Zanetti, Curtis C Harris, Stephen Chanock, James McKay, Ann G Schwartz, Rayjean J Hung, Christopher I Amos
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引用次数: 0

Abstract

Despite lung cancer affecting all races and ethnicities, disparities are observed in incidence and mortality rates among different ethnic groups in the United States. Non-Hispanic African Americans had a high incidence rate of lung cancer at 55.8 per 100 000 people, as well as the highest death rate at 37.2 per 100 000 people from 2016 to 2020. While previous genome-wide association studies (GWAS) have identified over 45 susceptibility risk loci that influence lung cancer development, few GWAS have investigated the etiology of lung cancer in African Americans. To address this gap in knowledge, we conducted GWAS of lung cancer focused on studying African Americans, comprising 2267 lung cancer cases and 4264 controls. We identified three loci associated with lung cancer, one with lung adenocarcinoma, and four with lung squamous cell carcinoma in this population at the genomic-wide significance level. Among them, three novel loci were identified near VWF at 12p13.31 for overall lung cancer and GACAT3 at 2p24.3 and LMAN1L at 15q24.1 for lung squamous cell carcinoma. In addition, we confirmed previously reported risk loci with known or new lead variants near CHRNA5 at 15q25.1 and CYP2A6 at 19q13.2 associated with lung cancer and TRIP13 at 5p15.33 and ERC1 at 12p13.33 associated with lung squamous cell carcinoma. Further multi-step functional analyses shed light on biological mechanisms underlying these associations of lung cancer in this population. Our study highlights the importance of ancestry-specific studies for the potential alleviation of lung cancer burden in African Americans.

6531例非裔美国人肺癌全基因组关联研究揭示新的易感位点
尽管肺癌影响所有种族和民族,但在美国不同种族群体之间的发病率和死亡率存在差异。2016年至2020年,非西班牙裔非洲裔美国人的肺癌发病率很高,为每10万人55.8例,死亡率最高,为每10万人37.2例。虽然以前的全基因组关联研究(GWAS)已经确定了超过45个影响肺癌发展的易感风险位点,但很少有GWAS研究非裔美国人肺癌的病因。为了解决这一知识缺口,我们对非裔美国人进行了肺癌GWAS研究,包括2267例肺癌病例和4264例对照。我们在全基因组显著水平上确定了三个与肺癌相关的基因座,一个与肺腺癌相关,四个与肺鳞状细胞癌相关。其中,在VWF附近发现了3个新的基因座,在整体肺癌中为12p13.31位点,在肺鳞状细胞癌中为2p24.3位点,在LMAN1L位点为15q24.1位点。此外,我们证实了先前报道的已知或新的铅变异体风险位点靠近CHRNA5基因15q25.1和CYP2A6基因19q13.2与肺癌相关,TRIP13基因5p15.33和ERC1基因12p13.33与肺鳞状细胞癌相关。进一步的多步骤功能分析揭示了这一人群中肺癌相关的生物学机制。我们的研究强调了对非裔美国人肺癌负担的潜在减轻进行特定血统研究的重要性。
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来源期刊
Human molecular genetics
Human molecular genetics 生物-生化与分子生物学
CiteScore
6.90
自引率
2.90%
发文量
294
审稿时长
2-4 weeks
期刊介绍: Human Molecular Genetics concentrates on full-length research papers covering a wide range of topics in all aspects of human molecular genetics. These include: the molecular basis of human genetic disease developmental genetics cancer genetics neurogenetics chromosome and genome structure and function therapy of genetic disease stem cells in human genetic disease and therapy, including the application of iPS cells genome-wide association studies mouse and other models of human diseases functional genomics computational genomics In addition, the journal also publishes research on other model systems for the analysis of genes, especially when there is an obvious relevance to human genetics.
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