• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Association between GWAS-identified lung adenocarcinoma susceptibility loci and EGFR mutations in never-smoking Asian women, and comparison with findings from Western populations.全基因组关联研究(GWAS)确定的肺腺癌易感基因座与从不吸烟的亚洲女性表皮生长因子受体(EGFR)突变之间的关联,以及与西方人群研究结果的比较。
Hum Mol Genet. 2017 Jan 15;26(2):454-465. doi: 10.1093/hmg/ddw414.
2
A genome-wide association study identifies two new susceptibility loci for lung adenocarcinoma in the Japanese population.全基因组关联研究在日本人群中鉴定出肺腺癌的两个新的易感位点。
Nat Genet. 2012 Jul 15;44(8):900-3. doi: 10.1038/ng.2353.
3
Genetic predisposition to lung adenocarcinoma among never-smoking Chinese with different epidermal growth factor receptor mutation status.不同表皮生长因子受体突变状态的中国不吸烟人群中肺腺癌的遗传易感性。
Lung Cancer. 2017 Dec;114:79-89. doi: 10.1016/j.lungcan.2017.10.012. Epub 2017 Oct 31.
4
Association of variations in HLA class II and other loci with susceptibility to EGFR-mutated lung adenocarcinoma.HLA Ⅱ类和其他位点的变异与 EGFR 突变型肺腺癌易感性的关联。
Nat Commun. 2016 Aug 9;7:12451. doi: 10.1038/ncomms12451.
5
Replication of lung cancer susceptibility loci at chromosomes 15q25, 5p15, and 6p21: a pooled analysis from the International Lung Cancer Consortium.肺癌易感性基因座 15q25、5p15 和 6p21 的复制:国际肺癌联盟的荟萃分析。
J Natl Cancer Inst. 2010 Jul 7;102(13):959-71. doi: 10.1093/jnci/djq178. Epub 2010 Jun 14.
6
Genome-wide association analysis identifies new lung cancer susceptibility loci in never-smoking women in Asia.全基因组关联分析鉴定出亚洲从不吸烟女性肺癌的新易感基因位点。
Nat Genet. 2012 Dec;44(12):1330-5. doi: 10.1038/ng.2456. Epub 2012 Nov 11.
7
EGFR polymorphisms, hormone replacement therapy and lung adenocarcinoma risk: analysis from a genome-wide association study in never-smoking women.EGFR 多态性、激素替代疗法与肺腺癌风险:从不吸烟女性全基因组关联研究分析。
Carcinogenesis. 2013 Mar;34(3):612-9. doi: 10.1093/carcin/bgs385. Epub 2012 Dec 13.
8
Spectrum of oncogenic driver mutations in lung adenocarcinomas from East Asian never smokers.东亚从不吸烟肺腺癌的致癌驱动基因突变谱。
PLoS One. 2011;6(11):e28204. doi: 10.1371/journal.pone.0028204. Epub 2011 Nov 30.
9
Lung cancer in never-smoker Asian females is driven by oncogenic mutations, most often involving EGFR.从不吸烟的亚洲女性肺癌是由致癌突变驱动的,其中最常见的是涉及表皮生长因子受体(EGFR)。
Oncotarget. 2015 Mar 10;6(7):5465-74. doi: 10.18632/oncotarget.2925.
10
Genetic variant in TP63 on locus 3q28 is associated with risk of lung adenocarcinoma among never-smoking females in Asia.TP63 基因座 3q28 上的遗传变异与亚洲从不吸烟女性肺腺癌的风险相关。
Hum Genet. 2012 Jul;131(7):1197-203. doi: 10.1007/s00439-012-1144-8. Epub 2012 Feb 25.

引用本文的文献

1
Early-onset lung cancer in Asia: a narrative review.亚洲早发性肺癌:一篇叙述性综述。
Front Oncol. 2025 Aug 4;15:1631443. doi: 10.3389/fonc.2025.1631443. eCollection 2025.
2
An online explainable ensemble machine learning model for predicting epidermal growth factor receptor mutation status in lung adenocarcinoma.一种用于预测肺腺癌中表皮生长因子受体突变状态的在线可解释集成机器学习模型。
Transl Lung Cancer Res. 2025 Jul 31;14(7):2670-2687. doi: 10.21037/tlcr-2025-237. Epub 2025 Jul 28.
3
Image harmonization and de-harmonization based on singular value decomposition (SVD) in medical domain.基于奇异值分解(SVD)的医学领域图像协调与去协调
Quant Imaging Med Surg. 2025 Aug 1;15(8):7062-7079. doi: 10.21037/qims-24-2225. Epub 2025 Jul 30.
4
Potential Influence of Genetic Variants and Expression Levels on the Mutation Status and Disease Progression in Patients with Lung Adenocarcinoma.基因变异和表达水平对肺腺癌患者突变状态及疾病进展的潜在影响
Int J Mol Sci. 2025 May 11;26(10):4606. doi: 10.3390/ijms26104606.
5
Predictive performance of risk prediction models for lung cancer incidence in Western and Asian countries: a systematic review and meta-analysis.西方国家和亚洲国家肺癌发病风险预测模型的预测性能:一项系统评价和荟萃分析。
Sci Rep. 2025 Mar 4;15(1):4259. doi: 10.1038/s41598-024-83875-6.
6
Comprehensive Analysis of circRNA-Related mRNAs as Prognostic Factors in Non-Smoking Women with Lung Adenocarcinoma.环状RNA相关mRNA作为非吸烟女性肺腺癌预后因素的综合分析
Int J Gen Med. 2024 Dec 3;17:5757-5771. doi: 10.2147/IJGM.S490478. eCollection 2024.
7
Enhancing disease risk gene discovery by integrating transcription factor-linked trans-variants into transcriptome-wide association analyses.通过将转录因子相关的反式变异整合到全转录组关联分析中来增强疾病风险基因的发现。
Nucleic Acids Res. 2025 Jan 7;53(1). doi: 10.1093/nar/gkae1035.
8
Discriminating bronchiolar adenoma from peripheral lung cancer by thin-section computed tomography (CT): a 2-center study.通过薄层计算机断层扫描(CT)鉴别细支气管腺瘤与周围型肺癌:一项双中心研究。
Quant Imaging Med Surg. 2024 Oct 1;14(10):7086-7097. doi: 10.21037/qims-24-687. Epub 2024 Aug 19.
9
Association of rs401681 (C > T) and rs402710 (C > T) polymorphisms in the CLPTM1L region with risk of lung cancer: a systematic review and meta-analysis.CLPTM1L 区域 rs401681(C > T)和 rs402710(C > T)多态性与肺癌风险的关联:系统评价和荟萃分析。
Sci Rep. 2024 Sep 30;14(1):22603. doi: 10.1038/s41598-024-73254-6.
10
GWAS advancements to investigate disease associations and biological mechanisms.全基因组关联研究(GWAS)在探究疾病关联和生物学机制方面的进展。
Clin Transl Discov. 2024 Jul;4(3). doi: 10.1002/ctd2.296. Epub 2024 May 1.

本文引用的文献

1
Association of variations in HLA class II and other loci with susceptibility to EGFR-mutated lung adenocarcinoma.HLA Ⅱ类和其他位点的变异与 EGFR 突变型肺腺癌易感性的关联。
Nat Commun. 2016 Aug 9;7:12451. doi: 10.1038/ncomms12451.
2
Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women.全基因组关联研究的荟萃分析确定了从不吸烟的亚洲女性中的多个肺癌易感基因座。
Hum Mol Genet. 2016 Feb 1;25(3):620-9. doi: 10.1093/hmg/ddv494. Epub 2016 Jan 4.
3
Fine mapping of chromosome 5p15.33 based on a targeted deep sequencing and high density genotyping identifies novel lung cancer susceptibility loci.基于靶向深度测序和高密度基因分型对5号染色体5p15.33区域进行精细定位,鉴定出新型肺癌易感位点。
Carcinogenesis. 2016 Jan;37(1):96-105. doi: 10.1093/carcin/bgv165. Epub 2015 Nov 20.
4
BPTF promotes tumor growth and predicts poor prognosis in lung adenocarcinomas.BPTF促进肺腺癌的肿瘤生长并预示不良预后。
Oncotarget. 2015 Oct 20;6(32):33878-92. doi: 10.18632/oncotarget.5302.
5
Identification of lung cancer histology-specific variants applying Bayesian framework variant prioritization approaches within the TRICL and ILCCO consortia.在TRICL和ILCCO联盟中应用贝叶斯框架变异优先级排序方法鉴定肺癌组织学特异性变异。
Carcinogenesis. 2015 Nov;36(11):1314-26. doi: 10.1093/carcin/bgv128. Epub 2015 Sep 10.
6
Epidemiology of lung cancer in China.中国肺癌流行病学。
Thorac Cancer. 2015 Mar;6(2):209-15. doi: 10.1111/1759-7714.12169. Epub 2015 Mar 2.
7
Peptide Nucleic Acid Clamping Versus Direct Sequencing for the Detection of EGFR Gene Mutation in Patients with Non-small Cell Lung Cancer.肽核酸钳夹法与直接测序法在非小细胞肺癌患者表皮生长因子受体基因突变检测中的比较
Cancer Res Treat. 2015 Oct;47(4):661-9. doi: 10.4143/crt.2014.282. Epub 2015 Feb 23.
8
Cancer incidence and mortality worldwide: sources, methods and major patterns in GLOBOCAN 2012.全球癌症发病与死亡:GLOBOCAN 2012 数据源、方法与主要模式。
Int J Cancer. 2015 Mar 1;136(5):E359-86. doi: 10.1002/ijc.29210. Epub 2014 Oct 9.
9
Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer.BRCA2和CHEK2中具有大效应的罕见变异会影响肺癌风险。
Nat Genet. 2014 Jul;46(7):736-41. doi: 10.1038/ng.3002. Epub 2014 Jun 1.
10
Pleiotropic associations of risk variants identified for other cancers with lung cancer risk: the PAGE and TRICL consortia.其他癌症风险变异与肺癌风险的多效关联:PAGE 和 TRICL 联盟。
J Natl Cancer Inst. 2014 Apr;106(4):dju061. doi: 10.1093/jnci/dju061. Epub 2014 Mar 28.

全基因组关联研究(GWAS)确定的肺腺癌易感基因座与从不吸烟的亚洲女性表皮生长因子受体(EGFR)突变之间的关联,以及与西方人群研究结果的比较。

Association between GWAS-identified lung adenocarcinoma susceptibility loci and EGFR mutations in never-smoking Asian women, and comparison with findings from Western populations.

作者信息

Seow Wei Jie, Matsuo Keitaro, Hsiung Chao Agnes, Shiraishi Kouya, Song Minsun, Kim Hee Nam, Wong Maria Pik, Hong Yun-Chul, Hosgood H Dean, Wang Zhaoming, Chang I-Shou, Wang Jiu-Cun, Chatterjee Nilanjan, Tucker Margaret, Wei Hu, Mitsudomi Tetsuya, Zheng Wei, Kim Jin Hee, Zhou Baosen, Caporaso Neil E, Albanes Demetrius, Shin Min-Ho, Chung Lap Ping, An She-Juan, Wang Ping, Zheng Hong, Yatabe Yasushi, Zhang Xu-Chao, Kim Young Tae, Shu Xiao-Ou, Kim Young-Chul, Bassig Bryan A, Chang Jiang, Ho James Chung Man, Ji Bu-Tian, Kubo Michiaki, Daigo Yataro, Ito Hidemi, Momozawa Yukihide, Ashikawa Kyota, Kamatani Yoichiro, Honda Takayuki, Sakamoto Hiromi, Kunitoh Hideo, Tsuta Koji, Watanabe Shun-Ichi, Nokihara Hiroshi, Miyagi Yohei, Nakayama Haruhiko, Matsumoto Shingo, Tsuboi Masahiro, Goto Koichi, Yin Zhihua, Shi Jianxin, Takahashi Atsushi, Goto Akiteru, Minamiya Yoshihiro, Shimizu Kimihiro, Tanaka Kazumi, Wu Tangchun, Wei Fusheng, Wong Jason Y Y, Matsuda Fumihiko, Su Jian, Kim Yeul Hong, Oh In-Jae, Song Fengju, Lee Victor Ho Fun, Su Wu-Chou, Chen Yuh-Min, Chang Gee-Chen, Chen Kuan-Yu, Huang Ming-Shyan, Yang Pan-Chyr, Lin Hsien-Chih, Xiang Yong-Bing, Seow Adeline, Park Jae Yong, Kweon Sun-Seog, Chen Chien-Jen, Li Haixin, Gao Yu-Tang, Wu Chen, Qian Biyun, Lu Daru, Liu Jianjun, Jeon Hyo-Sung, Hsiao Chin-Fu, Sung Jae Sook, Tsai Ying-Huang, Jung Yoo Jin, Guo Huan, Hu Zhibin, Wang Wen-Chang, Chung Charles C, Lawrence Charles, Burdett Laurie, Yeager Meredith, Jacobs Kevin B, Hutchinson Amy, Berndt Sonja I, He Xingzhou, Wu Wei, Wang Junwen, Li Yuqing, Choi Jin Eun, Park Kyong Hwa, Sung Sook Whan, Liu Li, Kang Chang Hyun, Hu Lingmin, Chen Chung-Hsing, Yang Tsung-Ying, Xu Jun, Guan Peng, Tan Wen, Wang Chih-Liang, Sihoe Alan Dart Loon, Chen Ying, Choi Yi Young, Hung Jen-Yu, Kim Jun Suk, Yoon Ho-Il, Cai Qiuyin, Lin Chien-Chung, Park In Kyu, Xu Ping, Dong Jing, Kim Christopher, He Qincheng, Perng Reury-Perng, Chen Chih-Yi, Vermeulen Roel, Wu Junjie, Lim Wei-Yen, Chen Kun-Chieh, Chan John K C, Chu Minjie, Li Yao-Jen, Li Jihua, Chen Hongyan, Yu Chong-Jen, Jin Li, Lo Yen-Li, Chen Ying-Hsiang, Fraumeni Joseph F, Liu Jie, Yamaji Taiki, Yang Yang, Hicks Belynda, Wyatt Kathleen, Li Shengchao A, Dai Juncheng, Ma Hongxia, Jin Guangfu, Song Bao, Wang Zhehai, Cheng Sensen, Li Xuelian, Ren Yangwu, Cui Ping, Iwasaki Motoki, Shimazu Taichi, Tsugane Shoichiro, Zhu Junjie, Jiang Gening, Fei Ke, Wu Guoping, Chien Li-Hsin, Chen Hui-Ling, Su Yu-Chun, Tsai Fang-Yu, Chen Yi-Song, Yu Jinming, Stevens Victoria L, Laird-Offringa Ite A, Marconett Crystal N, Lin Dongxin, Chen Kexin, Wu Yi-Long, Landi Maria Teresa, Shen Hongbing, Rothman Nathaniel, Kohno Takashi, Chanock Stephen J, Lan Qing

机构信息

Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD, USA.

Saw Swee Hock School of Public Health, National University of Singapore and National University Health System, Singapore.

出版信息

Hum Mol Genet. 2017 Jan 15;26(2):454-465. doi: 10.1093/hmg/ddw414.

DOI:10.1093/hmg/ddw414
PMID:28025329
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5856088/
Abstract

To evaluate associations by EGFR mutation status for lung adenocarcinoma risk among never-smoking Asian women, we conducted a meta-analysis of 11 loci previously identified in genome-wide association studies (GWAS). Genotyping in an additional 10,780 never-smoking cases and 10,938 never-smoking controls from Asia confirmed associations with eight known single nucleotide polymorphisms (SNPs). Two new signals were observed at genome-wide significance (P < 5 × 10-8), namely, rs7216064 (17q24.3, BPTF), for overall lung adenocarcinoma risk, and rs3817963 (6p21.3, BTNL2) which is specific to cases with EGFR mutations. In further sub-analyses by EGFR status, rs9387478 (ROS1/DCBLD1) and rs2179920 (HLA-DPB1) showed stronger estimated associations in EGFR-positive compared to EGFR-negative cases. Comparison of the overall associations with published results in Western populations revealed that the majority of these findings were distinct, underscoring the importance of distinct contributing factors for smoking and non-smoking lung cancer. Our results extend the catalogue of regions associated with lung adenocarcinoma in non-smoking Asian women and highlight the importance of how the germline could inform risk for specific tumour mutation patterns, which could have important translational implications.

摘要

为了评估从不吸烟的亚洲女性中表皮生长因子受体(EGFR)突变状态与肺腺癌风险之间的关联,我们对之前在全基因组关联研究(GWAS)中确定的11个基因座进行了荟萃分析。对另外10780例从不吸烟的病例和10938例从不吸烟的亚洲对照进行基因分型,证实了与8个已知单核苷酸多态性(SNP)的关联。在全基因组显著性水平(P < 5×10-8)观察到两个新信号,即rs7216064(17q24.3,BPTF)与总体肺腺癌风险相关,以及rs3817963(6p21.3,BTNL2)与EGFR突变病例特异性相关。在按EGFR状态进行的进一步亚组分析中,与EGFR阴性病例相比,rs9387478(ROS1/DCBLD1)和rs2179920(HLA-DPB1)在EGFR阳性病例中显示出更强的估计关联。将总体关联与西方人群已发表的结果进行比较,发现这些发现中的大多数是不同的,这突出了吸烟和非吸烟肺癌不同促成因素的重要性。我们的结果扩展了与从不吸烟的亚洲女性肺腺癌相关区域的目录,并强调了种系如何为特定肿瘤突变模式的风险提供信息的重要性,这可能具有重要的转化意义。