Rosati Rayna, Chen Bailing, Patki Mugdha, McFall Thomas, Ou Siyu, Heath Elisabeth, Ratnam Manohar, Qin Zhihui
Barbara Ann Karmanos Cancer Institute, Departments of Oncology (R.R., M.P., T.M., E.H., M.R.) and Pharmaceutical Sciences (B.C., S.O., Z.Q.), Wayne State University, Detroit, Michigan.
Barbara Ann Karmanos Cancer Institute, Departments of Oncology (R.R., M.P., T.M., E.H., M.R.) and Pharmaceutical Sciences (B.C., S.O., Z.Q.), Wayne State University, Detroit, Michigan
Mol Pharmacol. 2016 Sep;90(3):225-37. doi: 10.1124/mol.116.103416. Epub 2016 Jul 5.
Histone deacetylase inhibitors (HDACIs) can disrupt the viability of prostate cancer (PCa) cells through modulation of the cytosolic androgen receptor (AR) chaperone protein heat shock protein 90 (HSP90). However, toxicities associated with their pleiotropic effects could contribute to the ineffectiveness of HDACIs in PCa treatment. We designed hybrid molecules containing partial chemical scaffolds of enzalutamide and suberoylanilide hydroxamic acid (SAHA), with weakened intrinsic pan-HDACI activities, to target HSP90 and AR in enzalutamide-resistant PCa cells. The potency of the new molecules, compounds 2-75 [4-(3-(4-cyano-3-(trifluoromethyl)phenyl)-5,5-dimethyl-4-oxo-2-thioxoimidazolidin-1-yl)-2-fluoro-N-(7-(hydroxyamino)-7-oxoheptyl)benzamide] and 1005 [(E)-3-(4-(3-(4-cyano-3-(trifluoromethyl)phenyl)-5,5-dimethyl-4-oxo-2-thioxoimidazolidin-1-yl)-2-fluorophenyl)-N-hydroxyacrylamide], as inhibitors of nuclear and cytosolic histone deacetylases was substantially lower than that of SAHA in cell-free and in situ assays. Compounds 2-75 and 1005 antagonized gene activation by androgen without inducing chromatin association of AR. Enzalutamide had no effect on the levels of AR or HSP90, whereas the hybrid compounds induced degradation of both AR and HSP90, similar to (compound 1005) or more potently than (compound 2-75) SAHA. Similar to SAHA, compounds 2-75 and 1005 decreased the level of HSP90 and induced acetylation in a predicted approximately 55 kDa HSP90 fragment. Compared with SAHA, compound 2-75 induced greater hyperacetylation of the HDAC6 substrate α-tubulin. In contrast with SAHA, neither hybrid molecule caused substantial hyperacetylation of histones H3 and H4. Compounds 2-75 and 1005 induced p21 and caused loss of viability in the enzalutamide-resistant C4-2 cells, with efficacies that were comparable to or better than SAHA. The results suggest the potential of the new compounds as prototype antitumor drugs that would downregulate HSP90 and AR in enzalutamide-resistant PCa cells with weakened effects on nuclear HDACI targets.
组蛋白去乙酰化酶抑制剂(HDACIs)可通过调节胞质雄激素受体(AR)伴侣蛋白热休克蛋白90(HSP90)来破坏前列腺癌细胞(PCa)的活力。然而,与其多效性作用相关的毒性可能导致HDACIs在PCa治疗中无效。我们设计了含有恩杂鲁胺和辛二酰苯胺异羟肟酸(SAHA)部分化学支架的杂合分子,其内在的泛HDACIs活性减弱,以靶向恩杂鲁胺耐药PCa细胞中的HSP90和AR。新分子化合物2 - 75 [4-(3-(4-氰基-3-(三氟甲基)苯基)-5,5-二甲基-4-氧代-2-硫代咪唑烷-1-基)-2-氟-N-(7-(羟基氨基)-7-氧代庚基)苯甲酰胺]和1005 [(E)-3-(4-(3-(4-氰基-3-(三氟甲基)苯基)-5,5-二甲基-4-氧代-2-硫代咪唑烷-1-基)-2-氟苯基)-N-羟基丙烯酰胺]作为核和胞质组蛋白去乙酰化酶抑制剂,在无细胞和原位测定中其效力明显低于SAHA。化合物2 - 75和1005可拮抗雄激素诱导的基因激活,而不诱导AR的染色质结合。恩杂鲁胺对AR或HSP90水平无影响,而杂合化合物可诱导AR和HSP90降解,与SAHA相似(化合物1005)或比SAHA更有效(化合物2 - 75)。与SAHA相似,化合物2 - 75和化合物1005降低了HSP90水平,并在预测的约55 kDa HSP90片段中诱导乙酰化。与SAHA相比,化合物2 - 75诱导HDAC6底物α-微管蛋白发生更大程度的高乙酰化。与SAHA不同, 两种杂合分子均未引起组蛋白H3和H4的大量高乙酰化。化合物2 - 75和1005诱导p21表达,并导致恩杂鲁胺耐药的C4 - 2细胞活力丧失,其疗效与SAHA相当或优于SAHA。结果表明,这些新化合物具有作为原型抗肿瘤药物的潜力,可下调恩杂鲁胺耐药PCa细胞中的HSP90和AR,同时对核HDACIs靶点的影响减弱。