遗传性甲基化标记与前列腺癌风险有关。

IF 1.8 4区 医学 Q3 GENETICS & HEREDITY
Familial Cancer Pub Date : 2023-07-01 Epub Date: 2023-01-28 DOI:10.1007/s10689-022-00325-w
James G Dowty, Chenglong Yu, Mahnaz Hosseinpour, Jihoon Eric Joo, Ee Ming Wong, Tu Nguyen-Dumont, Joseph Rosenbluh, Graham G Giles, Roger L Milne, Robert J MacInnis, Pierre-Antoine Dugué, Melissa C Southey
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引用次数: 0

摘要

众所周知,父母遗传给后代的 DNA 甲基化标记在癌症风险中起着一定的作用,可以解释部分家族性癌症风险。因此,我们在全基因组范围内寻找与前列腺癌风险相关的遗传甲基化标记。我们使用 EPIC 阵列对 25 个多病例前列腺癌家族 469 名成员中的 133 人进行了外周血 DNA 甲基化检测。我们利用这些家族系统地搜索基因组中具有孟德尔遗传模式的甲基化标记,然后测试了 1000 个遗传性最强的标记是否与前列腺癌风险有关。经多重检验校正后,41 个遗传甲基化标记与前列腺癌风险有关。根据一项前瞻性队列研究中的 869 例发病病例和 869 例对照进行的单独分析表明,这些标记中有 9 个靠近可转移的外显子 VTRNA2-1 也与人群中患侵袭性前列腺癌的风险有名义上的关联。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Heritable methylation marks associated with prostate cancer risk.

DNA methylation marks that are inherited from parents to offspring are known to play a role in cancer risk and could explain part of the familial risk for cancer. We therefore conducted a genome-wide search for heritable methylation marks associated with prostate cancer risk. Peripheral blood DNA methylation was measured for 133 of the 469 members of 25 multiple-case prostate cancer families, using the EPIC array. We used these families to systematically search the genome for methylation marks with Mendelian patterns of inheritance, then we tested the 1,000 most heritable marks for association with prostate cancer risk. After correcting for multiple testing, 41 heritable methylation marks were associated with prostate cancer risk. Separate analyses, based on 869 incident cases and 869 controls from a prospective cohort study, showed that 9 of these marks near the metastable epiallele VTRNA2-1 were also nominally associated with aggressive prostate cancer risk in the population.

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来源期刊
Familial Cancer
Familial Cancer 医学-遗传学
CiteScore
4.10
自引率
4.50%
发文量
36
审稿时长
6-12 weeks
期刊介绍: In recent years clinical cancer genetics has become increasingly important. Several events, in particular the developments in DNA-based technology, have contributed to this evolution. Clinical cancer genetics has now matured to a medical discipline which is truly multidisciplinary in which clinical and molecular geneticists work together with clinical and medical oncologists as well as with psycho-social workers. Due to the multidisciplinary nature of clinical cancer genetics most papers are currently being published in a wide variety of journals on epidemiology, oncology and genetics. Familial Cancer provides a forum bringing these topics together focusing on the interests and needs of the clinician. The journal mainly concentrates on clinical cancer genetics. Most major areas in the field shall be included, such as epidemiology of familial cancer, molecular analysis and diagnosis, clinical expression, treatment and prevention, counselling and the health economics of familial cancer.
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