DNA Methylation and miRNAs Regulation in Hereditary Breast Cancer: Epigenetic Changes, Players in Transcriptional and Post-Transcriptional Regulation in Hereditary Breast Cancer

被引:21
作者
Pinto, R. [1 ]
De Summa, S. [1 ]
Pilato, B. [1 ]
Tommasi, S. [1 ]
机构
[1] IRCCS Giovanni Paolo II, Mol Genet Lab, I-70124 Bari, Italy
关键词
Basal-like breast cancer; BRCA1; hereditary breast cancer; methylation; miRNA; triple-negative breast cancer; ESTROGEN-RECEPTOR-ALPHA; BRCA1 PROMOTER METHYLATION; BLOOD-BASED MARKERS; FAMILIAL BREAST; SPORADIC BREAST; CIRCULATING MICRORNAS; TAMOXIFEN RESISTANCE; EXPRESSION ANALYSIS; GENE METHYLATION; DOWN-REGULATION;
D O I
10.2174/1566524013666131203101405
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The genetic alterations associated with breast carcinogenesis are well known. On the contrary epigenetic alterations in hereditary breast cancer are a new field. Two epigenetic mechanisms have emerged as the most critical players in transcriptional regulation in breast cancer: the methylation of DNA and microRNA interference. In this review we will focus on recent findings on gene silencing caused by DNA methylation and microRNA to explore the potential role of these epigenetic changes in the understanding of hereditary breast cancer. Moreover we will describe the same alterations in basal-like breast cancer and in triple-negative breast cancer, since their phenotypes have similarities with BRCA1-mutated tumors. To underline the possibility that some epigenetic alterations could also be used as potential epigenetic biomarkers of drug sensitivity or resistance, we will discuss the more common therapies in hereditary breast cancer that could also be applied to breast cancer with basal-like or triple negative phenotypes.
引用
收藏
页码:45 / 57
页数:13
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