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Clinical epigenetics. 2016 Nov 25:8:127. doi: 10.1186/s13148-016-0292-4 Q14.82024

Smoking-associated DNA methylation markers predict lung cancer incidence

吸烟相关DNA甲基化标志物可预测肺癌发病风险 翻译改进

Yan Zhang  1, Magdeldin Elgizouli  2, Ben Schöttker  1, Bernd Holleczek  3, Alexandra Nieters  2, Hermann Brenner  1  4  5

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作者单位

  • 1 Division of Clinical Epidemiology and Aging Research, German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • 2 Center for Chronic Immunodeficiency (CCI), Research Group Epidemiology, University Medical Center Freiburg, Freiburg, Germany.
  • 3 Saarland Cancer Registry, Saarbrücken, Germany.
  • 4 Division of Preventive Oncology, German Cancer Research Center (DKFZ) and National Center for Tumor Diseases (NCT), Heidelberg, Germany.
  • 5 German Cancer Consortium (DKTK), German Cancer Research Center (DKFZ), Heidelberg, Germany.
  • DOI: 10.1186/s13148-016-0292-4 PMID: 27924164

    摘要 Ai翻译

    Background: Newly established blood DNA methylation markers that are strongly associated with smoking might open new avenues for lung cancer (LC) screening. We aimed to assess the performance of the top hits from previous epigenome-wide association studies in prediction of LC incidence. In a prospective nested case-control study, DNA methylation at AHRR (cg05575921), 6p21.33 (cg06126421), and F2RL3 (cg03636183) were measured by pyrosequencing in baseline whole blood samples of 143 incident LC cases identified during 11 years of follow-up and 457 age- and sex-matched controls without diagnosis of LC until the end of follow-up. The individual and joint associations of the 3 markers with LC risk were estimated by logistic regression, adjusted for potential confounders including smoking status and cigarette pack-years. The predictive performance was evaluated for both the individual markers and their combinations derived from multiple algorithms.

    Results: Pronounced demethylation of all 3 markers was observed at baseline among cases compared to controls. Risk of developing LC increased with decreasing DNA methylation levels, with adjusted ORs (95% CI) of 15.86 (4.18-60.17), 8.12 (2.69-4.48), and 10.55 (3.44-32.31), respectively, for participants in the lowest quartile of AHRR, 6p21.33, and F2RL3 compared to participants in the highest 2 quartiles of each site among controls. The individual 3 markers exhibited similar accuracy in predicting LC incidence, with AUCs ranging from 0.79 to 0.81. Combination of the 3 markers did not improve the predictive performance (AUC = 0.80). The individual markers or their combination outperformed self-reported smoking exposure particularly in light smokers. No variation in risk prediction was identified with respect to age, follow-up time, and histological subtypes.

    Conclusions: AHRR, 6p21.33, and F2RL3 methylation in blood DNA are predictive for LC development, which might be useful for identification of risk groups for further specific screening, such as CT examination.

    Keywords: AHRR; DNA methylation; F2RL3; Lung cancer; Risk prediction; Smoking.

    Keywords:lung cancer incidence

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    期刊名:Clinical epigenetics

    缩写:CLIN EPIGENETICS

    ISSN:1868-7083

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    IF/分区:4.8/Q1

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    Smoking-associated DNA methylation markers predict lung cancer incidence