维生素D受体激动剂/组蛋白去乙酰化酶抑制剂杂交分子的高激动性。

IF 6.8 1区 医学 Q1 CHEMISTRY, MEDICINAL
Fatemeh Sarmadi,Amelia Caza,Zhizhong Gao,Natacha Rochel,James L Gleason,John H White
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引用次数: 0

摘要

1,25-二羟基维生素D (1,25D)类似物与维生素D受体(VDR)结合,具有抗癌和免疫调节作用。虽然肿瘤经常抵抗1,25 d单药治疗,但将VDR激动剂与组蛋白去乙酰化酶抑制剂(HDACi)联合使用可以恢复抗癌效果。在这里,我们提出了AC-340,一种新的双功能分子,将HDACi纳入VDR激动剂主链。除了在体外多种黑色素瘤模型中具有强大的双功能外,对B16-F10小鼠黑色素瘤细胞的RNaseq分析显示,AC-340可超诱导多种VDR靶基因的表达。比较结构研究和ChIP-qPCR结果显示,AC-340与VDR共激活物结合域残基形成的相互作用比1,25 d多,从而更有效地募集共激活物CBP。这可能与AC-340 HDACi活性相结合,导致VDR靶基因的H3K27乙酰化升高,这是转录活跃的标志。因此,AC-340作为一种VDR高激动剂,在针对多种癌症模型的单一或联合治疗中应该是有效的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hyperagonism of a Vitamin D Receptor Agonist/Histone Deacetylase Inhibitor Hybrid Molecule.
1,25-Dihydroxyvitamin D (1,25D) analogs engage the vitamin D receptor (VDR) and can exert anticancer and immunomodulatory effects. Although tumors often resist 1,25D monotherapy, combining VDR agonism with histone deacetylase inhibitors (HDACi) restores anticancer efficacy. Here, we present AC-340, a novel bifunctional molecule that incorporates HDACi into a VDR agonist backbone. Besides its robust bifunctionality in vitro in multiple melanoma models, RNaseq analysis of B16-F10 mouse melanoma cells revealed that AC-340 superinduces the expression of a broad array of VDR target genes. Comparative structural studies and ChIP-qPCR revealed that AC-340 forms more interactions than 1,25D with residues in the VDR coactivator binding domain, leading to more efficacious recruitment of coactivator CBP. This, likely coupled with AC-340 HDACi activity, leads to elevated H3K27 acetylation of VDR target genes, a mark of active transcription. Thus, AC-340 functions as a VDR hyperagonist and should be efficacious in mono- or combination therapies against multiple cancer models.
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来源期刊
Journal of Medicinal Chemistry
Journal of Medicinal Chemistry 医学-医药化学
CiteScore
4.00
自引率
11.00%
发文量
804
审稿时长
1.9 months
期刊介绍: The Journal of Medicinal Chemistry is a prestigious biweekly peer-reviewed publication that focuses on the multifaceted field of medicinal chemistry. Since its inception in 1959 as the Journal of Medicinal and Pharmaceutical Chemistry, it has evolved to become a cornerstone in the dissemination of research findings related to the design, synthesis, and development of therapeutic agents. The Journal of Medicinal Chemistry is recognized for its significant impact in the scientific community, as evidenced by its 2022 impact factor of 7.3. This metric reflects the journal's influence and the importance of its content in shaping the future of drug discovery and development. The journal serves as a vital resource for chemists, pharmacologists, and other researchers interested in the molecular mechanisms of drug action and the optimization of therapeutic compounds.
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