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共济失调毛细血管扩张症突变基因rs56009889与常见癌症风险

Ataxia telangiectasia-mutated rs56009889 and risk of common cancers.

作者信息

Barnet-Griness Ofra, Gruber Stephen B, Lipkin Steven M, Shulman Katerina, Haddad Riad, Galili Ronen, Rennert Gad

机构信息

Department of Community Medicine and Epidemiology, Carmel Medical Center, Haifa, Israel.

Precision Medicine Program, City of Hope, Duarte, California.

出版信息

Eur J Cancer Prev. 2025 Mar 1;34(2):124-129. doi: 10.1097/CEJ.0000000000000906. Epub 2024 Jul 16.

Abstract

A polymorphic variant in the ataxia telangiectasia-mutated ( ATM ) gene, rs56009889, was recently associated with an increased risk of lung cancer. We studied the role of this variant in the etiology of other cancers. Data from three population-based case-control studies of colon, breast, and lung cancer were used. Participants in these studies (4517 cases, 3383 controls) underwent a genome-wide association study using 500K Illumina OncoArray. The frequency of the AG/AA genotypes differed between Ashkenazi (4.6%) and Sephardi (0.2%) Jews ( P  < 0.001). AG/AA frequency was significantly higher in Ashkenazi lung cancer (11.9%) than in controls (2.8%) [adjusted odds ratio (OR) = 5.4]. Females had a higher risk than males (OR = 12.8 versus 3.5). The adjusted OR for colorectal cancer was 1.40 [95% confidence interval (CI) = 1.01-2.0, P  = 0.045] and for breast cancer was 1.43 (95% CI = 1.01-2.04, P  = 0.046). Never-smokers variant carriers were at higher risk of lung and colon, but not breast, cancer. Cases with the AG/AA genotype had lower mean age at diagnosis, but this difference was significant only for breast cancer (-3.2 years, P  = 0.007). No associations were observed with overall survival. Among the breast cancer subjects, the OR for having triple-negative tumors was 0.45 for AG/AA versus GG genotype (95% CI = 0.2-0.9, P  = 0.02). We confirm the strong association between ATM rs56009889 and lung cancer risk in Ashkenazi Jews and report a mild association with the risk of breast cancer and colorectal cancer.

摘要

共济失调毛细血管扩张症突变(ATM)基因中的一个多态性变体rs56009889,最近被发现与肺癌风险增加有关。我们研究了该变体在其他癌症病因中的作用。使用了来自三项基于人群的结肠癌、乳腺癌和肺癌病例对照研究的数据。这些研究的参与者(4517例病例,3383例对照)使用500K Illumina OncoArray进行了全基因组关联研究。AG/AA基因型的频率在阿什肯纳兹犹太人(4.6%)和西班牙裔犹太人(0.2%)之间存在差异(P < 0.001)。阿什肯纳兹肺癌患者中AG/AA频率(11.9%)显著高于对照组(2.8%)[调整后的优势比(OR)= 5.4]。女性的风险高于男性(OR = 12.8对3.5)。结直肠癌的调整后OR为1.40 [95%置信区间(CI)= 1.01 - 2.0,P = 0.045],乳腺癌的调整后OR为1.43(95% CI = 1.01 - 2.04,P = 0.046)。从不吸烟的变体携带者患肺癌和结肠癌的风险较高,但患乳腺癌的风险不高。AG/AA基因型的病例诊断时的平均年龄较低,但这种差异仅在乳腺癌中显著(-3.2岁,P = 0.007)。未观察到与总生存期的关联。在乳腺癌受试者中,AG/AA基因型与GG基因型相比,患三阴性肿瘤的OR为0.45(95% CI = 0.2 - 0.9,P = 0.02)。我们证实了阿什肯纳兹犹太人中ATM rs56009889与肺癌风险之间的强关联,并报告了与乳腺癌和结直肠癌风险的轻度关联。

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