Azzollini Jacopo, Pesenti Chiara, Pizzamiglio Sara, Fontana Laura, Guarino Carmela, Peissel Bernard, Plebani Maddalena, Tabano Silvia, Sirchia Silvia Maria, Colapietro Patrizia, Villa Roberta, Paolini Biagio, Verderio Paolo, Miozzo Monica, Manoukian Siranoush
Unit of Medical Genetics, Department of Medical Oncology and Hematology, Fondazione IRCCS Istituto Nazionale dei Tumori, 20133 Milan, Italy.
Department of Pathophysiology & Transplantation, Università degli Studi di Milano; Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, 20122 Milano, Italy.
Cancers (Basel). 2019 Jan 9;11(1):58. doi: 10.3390/cancers11010058.
Early age at onset of breast cancer (eoBC) is suggestive of an increased genetic risk. Although genetic testing is offered to all eoBC-affected women, in isolated cases the detection rate of pathogenic variants is <10%. This study aimed at assessing the role of constitutive promoter methylation at BC-associated loci as an underlying predisposing event in women with eoBC and negative family history. Promoter methylation at 12 loci was assessed by the MassARRAY technology in blood from 154 negative patients with eoBC and negative family history, and 60 healthy controls. Hypermethylation was determined, within each promoter, by comparing the patient's mean methylation value with thresholds based on one-sided 95% bootstrap confidence interval of the controls' mean. Three patients had hypermethylated results, two at and one at . Analyses on tumor tissue from the patient exceeding the highest threshold at revealed a mean methylation >60% and loss of heterozygosity at chromosome 17q. The patient hypermethylated at showed low methylation in the tumor sample, ruling out a role for methylation-induced silencing in tumor development. In isolated eoBC patients, constitutive promoter methylation may be a predisposing event. Further studies are required to define the impact of methylation changes occurring at BC-predisposing genes and their role in tumorigenesis.
乳腺癌发病年龄早(eoBC)提示遗传风险增加。尽管对所有患eoBC的女性都提供了基因检测,但在个别病例中,致病变异的检出率<10%。本研究旨在评估BC相关基因座的组成型启动子甲基化在eoBC且家族史阴性的女性中作为潜在易患事件的作用。通过MassARRAY技术对154例eoBC且家族史阴性的阴性患者和60例健康对照者血液中的12个基因座的启动子甲基化进行评估。通过将患者的平均甲基化值与基于对照者平均值的单侧95%自展置信区间的阈值进行比较,在每个启动子内确定高甲基化。3例患者有高甲基化结果,2例在[具体基因座1],1例在[具体基因座2]。对在[具体基因座1]超过最高阈值的患者的肿瘤组织分析显示,平均甲基化>60%,且17号染色体q臂杂合性缺失。在[具体基因座2]高甲基化的患者在肿瘤样本中显示低甲基化,排除了甲基化诱导的沉默在肿瘤发生中的作用。在孤立的eoBC患者中,组成型启动子甲基化可能是一个易患事件。需要进一步研究来确定BC易感基因发生的甲基化变化的影响及其在肿瘤发生中的作用。