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靶向表观基因组作为乳腺癌的一种新治疗方法。

Targeting the Epigenome as a Novel Therapeutic Approach for Breast Cancer.

机构信息

Department of Biological Sciences, Sookmyung Women's University, 100, Cheongpa-ro 47-gil, Yongsan-gu, Seoul, 04310, South Korea.

出版信息

Adv Exp Med Biol. 2017;1026:287-313. doi: 10.1007/978-981-10-6020-5_14.

Abstract

Breast cancer is one of complex diseases that are influenced by environment. Various genetic and epigenetic alterations are provoking causes of breast carcinogenesis. Dynamic epigenetic regulation including DNA methylation and histone modification induces dysregulation of genes related to proliferation, apoptosis, and metastasis in breast cancer. DNA methylation is strongly associated with the repression of transcription through adding to the methyl group by DNA methyltransferases (DNMTs), and tumor suppressor genes such as CCND2 and RUNX3 have been investigated to undergo hypermethylation at promoter region in breast cancer. In addition, histone deacetylases (HDACs) contribute to transcriptional repression by removing acetyl group at lysine residues leading to tumorigenesis. Since epigenetic changes are reversible, therapeutic approaches have been applied with epigenetic modification drugs such as DNMT inhibitors and HDAC inhibitors. In this chapter, we will summarize the feature of epigenetic markers in breast cancer cells and the effect of single or combination of epigenetic reagents for breast cancer therapy.

摘要

乳腺癌是受环境影响的复杂疾病之一。各种遗传和表观遗传改变是引发乳腺癌发生的原因。动态表观遗传调控,包括 DNA 甲基化和组蛋白修饰,导致与乳腺癌增殖、凋亡和转移相关的基因失调。DNA 甲基化通过 DNA 甲基转移酶 (DNMTs) 向 DNA 添加甲基基团,与转录抑制强烈相关,并且已经研究了 CCND2 和 RUNX3 等肿瘤抑制基因在乳腺癌中启动子区域发生过度甲基化。此外,组蛋白去乙酰化酶 (HDACs) 通过去除赖氨酸残基上的乙酰基来促进转录抑制,导致肿瘤发生。由于表观遗传变化是可逆的,因此已经应用了治疗方法,包括使用表观遗传修饰药物,如 DNMT 抑制剂和 HDAC 抑制剂。在本章中,我们将总结乳腺癌细胞中表观遗传标记的特征,以及单一或联合使用表观遗传试剂治疗乳腺癌的效果。

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