Abeni Edoardo, Grossi Ilaria, Marchina Eleonora, Coniglio Arianna, Incardona Paolo, Cavalli Pietro, Zorzi Fausto, Chiodera Pier Luigi, Paties Carlo Terenzio, Crosatti Marialuisa, De Petro Giuseppina, Salvi Alessandro
Department of Molecular and Translational Medicine, Division of Biology and Genetics, University of Brescia, I-25123 Brescia, Italy.
Department of Clinical and Experimental Sciences, Surgical Clinic, University of Brescia, I-25123 Brescia, Italy.
Oncol Lett. 2021 Jun;21(6):468. doi: 10.3892/ol.2021.12729. Epub 2021 Apr 12.
In total, ~25% of familial breast cancer (BC) is attributed to germline mutations of the BRCA1 and BRCA2 genes, while the rest of the cases are included in the BRCAX group. BC is also known to affect men, with a worldwide incidence of 1%. Epigenetic alterations, including DNA methylation, have been rarely studied in male breast cancer (MBC) on a genome-wide level. The aim of the present study was to examine the global DNA methylation profiles of patients with BC to identify differences between familial female breast cancer (FBC) and MBC, and according to BRCA1, BRCA2 or BRCAX mutation status. The genomic DNA of formalin-fixed paraffin-embedded tissues from 17 women and 7 men with BC was subjected to methylated DNA immunoprecipitation and hybridized on human promoter microarrays. The comparison between FBC and MBC revealed 2,846 significant differentially methylated regions corresponding to 2,486 annotated genes. Gene Ontology enrichment analysis revealed molecular function terms, such as the GTPase superfamily genes (particularly the GTPase Rho GAP/GEF and GTPase RAB), and cellular component terms associated with cytoskeletal architecture, such as 'cytoskeletal part', 'keratin filament' and 'intermediate filament'. When only FBC was considered, several cancer-associated pathways were among the most enriched KEGG pathways of differentially methylated genes when the BRCA2 group was compared with the BRCAX or BRCA1+BRCAX groups. The comparison between the BRCA1 and BRCA2+BRCAX groups comprised the molecular function term 'cytoskeletal protein binding'. Finally, the functional annotation of differentially methylated genes between the BRCAX and BRCA1+BRCA2 groups indicated that the most enriched molecular function terms were associated with GTPase activity. In conclusion, to the best of our knowledge, the present study was the first to compare the global DNA methylation profile of familial FBC and MBC. The results may provide useful insights into the epigenomic subtyping of BC and shed light on a possible novel molecular mechanism underlying BC carcinogenesis.
总体而言,约25%的家族性乳腺癌(BC)归因于BRCA1和BRCA2基因的种系突变,其余病例则归入BRCAX组。已知BC也会影响男性,全球发病率为1%。包括DNA甲基化在内的表观遗传改变在男性乳腺癌(MBC)的全基因组水平上很少被研究。本研究的目的是检查BC患者的全基因组DNA甲基化谱,以确定家族性女性乳腺癌(FBC)和MBC之间以及根据BRCA1、BRCA2或BRCAX突变状态的差异。对17名患有BC的女性和7名患有BC的男性的福尔马林固定石蜡包埋组织的基因组DNA进行甲基化DNA免疫沉淀,并与人启动子微阵列杂交。FBC和MBC之间的比较揭示了2846个显著差异甲基化区域,对应于2486个注释基因。基因本体富集分析揭示了分子功能术语,如GTPase超家族基因(特别是GTPase Rho GAP/GEF和GTPase RAB),以及与细胞骨架结构相关的细胞成分术语,如“细胞骨架部分”、“角蛋白丝”和“中间丝”。当仅考虑FBC时,与癌症相关的几个途径是BRCA2组与BRCAX或BRCA1+BRCAX组比较时差异甲基化基因最富集的KEGG途径之一。BRCA1和BRCA2+BRCAX组之间的比较包括分子功能术语“细胞骨架蛋白结合”。最后,BRCAX和BRCA1+BRCA2组之间差异甲基化基因的功能注释表明,最富集的分子功能术语与GTPase活性相关。总之,据我们所知,本研究首次比较了家族性FBC和MBC的全基因组DNA甲基化谱。这些结果可能为BC的表观基因组亚型提供有用的见解,并揭示BC致癌作用潜在的一种可能的新分子机制。