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铁皮枫斗晶和萝卜硫素通过表观遗传机制调节乳腺癌细胞周期进程。

Withaferin A and sulforaphane regulate breast cancer cell cycle progression through epigenetic mechanisms.

机构信息

Department of Biology, University of Alabama at Birmingham, 1300 University Boulevard, 175 Campbell Hall, Birmingham, AL 35294, USA; Comprehensive Cancer Center, University of Alabama Birmingham, 1802 6th Avenue South, Birmingham, AL 35294, USA.

Department of Biology, University of Alabama at Birmingham, 1300 University Boulevard, 175 Campbell Hall, Birmingham, AL 35294, USA.

出版信息

Exp Cell Res. 2018 Jul 1;368(1):67-74. doi: 10.1016/j.yexcr.2018.04.015. Epub 2018 Apr 22.

DOI:10.1016/j.yexcr.2018.04.015
PMID:29689276
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6733260/
Abstract

Little is known about the effects of combinatorial dietary compounds on the regulation of epigenetic mechanisms involved in breast cancer prevention. The human diet consists of a multitude of components, and there is a need to elucidate how certain compounds interact in collaboration. Withaferin A (WA), found in the Indian winter cherry and documented as a DNA methyltransferase (DNMT) inhibitor, and sulforaphane (SFN), a well-known histone deacetylase (HDAC) inhibitor found in cruciferous vegetables, are two epigenetic modifying compounds that have only recently been studied in conjunction. The use of DNMT and HDAC inhibitors to reverse the malignant expression of certain genes in breast cancer has shown considerable promise. Previously, we found that SFN + WA synergistically promote breast cancer cell death. Herein, we determined that these compounds inhibit cell cycle progression from S to G2 phase in MDA-MB-231 and MCF-7 breast cancer. Furthermore, we demonstrate that this unique combination of epigenetic modifying compounds down-regulates the levels of Cyclin D1 and CDK4, and pRB; conversely, the levels of E2F mRNA and tumor suppressor p21 are increased independently of p53. We find these events coincide with an increase in unrestricted histone methylation. We propose SFN + WA-induced breast cancer cell death is attributed, in part, to epigenetic modifications that result in the modulated expression of key genes responsible for the regulation of cancer cell senescence.

摘要

关于组合饮食化合物对参与乳腺癌预防的表观遗传机制调节的影响知之甚少。人类饮食由多种成分组成,需要阐明某些化合物如何协同相互作用。冬樱中的白藜芦醇 A(WA)和十字花科蔬菜中发现的已知组蛋白去乙酰化酶(HDAC)抑制剂——萝卜硫素(SFN)是两种表观遗传修饰化合物,它们最近才被联合研究。使用 DNA 甲基转移酶(DNMT)和组蛋白去乙酰化酶(HDAC)抑制剂逆转乳腺癌中某些基因的恶性表达显示出相当大的前景。以前,我们发现 SFN+WA 协同促进乳腺癌细胞死亡。在此,我们确定这些化合物抑制 MDA-MB-231 和 MCF-7 乳腺癌细胞从 S 期到 G2 期的细胞周期进程。此外,我们证明这种独特的组合的表观遗传修饰化合物下调细胞周期蛋白 D1 和 CDK4 以及 pRB 的水平;相反,E2F mRNA 和肿瘤抑制因子 p21 的水平独立于 p53 增加。我们发现这些事件与不受限制的组蛋白甲基化增加相一致。我们提出 SFN+WA 诱导的乳腺癌细胞死亡部分归因于表观遗传修饰,导致负责调节癌细胞衰老的关键基因表达的调节。

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