Department of Pharmaceutical Sciences, University of Maryland School of Pharmacy, 20 Penn Street, Baltimore, MD 21201, USA.
J Pharmacol Exp Ther. 2012 Mar;340(3):688-97. doi: 10.1124/jpet.111.188854. Epub 2011 Dec 9.
Inhibition of insulin-like growth factor-1 receptor (IGF-1R) signaling represents an attractive therapeutic strategy for cancer treatment. A first-generation IGF-1R inhibitor (R)-4-(3-(3-chlorophenyl)-3-hydroxypropyl)-3-(4-methyl-6-morpholino-1H-benzo[d]imidazol-2-yl)pyridin-2(1H)-one (BMS-536924), however, was associated with potent CYP3A4 induction mediated by pregnane X receptor (PXR; NR1I2) transactivation. Structural activity-based modification led to the synthesis of 4-(1-(2-(4-((2-(4-chloro-1H-pyrazol-1-yl)ethyl)amino)-2-oxo-1,2-dihydropyridin-3-yl)-4-methyl-1H-benzo[d]imidazol-6-yl)piperidin-4-yl) piperazine-1-carboxylate (BMS-665351) with no PXR activity while maintaining its ability to inhibit IGF-1R. However, BMS-665351 significantly induces CYP3A4 expression in human primary hepatocytes (HPHs). Here, we report a novel nonclassical constitutive androstane receptor (CAR; NR1I3)-related pathway of BMS-665351-mediated CYP3A4 induction. BMS-665351 treatment resulted in the significant induction of CYP3A4 in HPHs and HepG2 cells, but failed to activate either PXR or CAR in cell-based reporter assays. Moreover, BMS-665351 at concentrations that induce CYP3A4 expression was unable to translocate human CAR from the cytoplasm to the nucleus of HPHs, which represents the initial step of CAR activation. Nevertheless, quantitative polymerase chain reaction analysis demonstrated that BMS-665351 significantly enhanced the expression of CYP3A4 in CAR- but not PXR-transfected HepG2 and Huh7 cells. It is noteworthy that BMS-665351 selectively induced the expression of CAR but not PXR in all tested hepatic cell systems. Synergistic induction of CYP3A4 was observed in HPHs cotreated with BMS-665351 and prototypical activators of CAR but not PXR. In summary, our results indicate that BMS-665351-mediated induction of CYP3A4 is CAR-dependent, but BMS-665351 itself is not a typical activator of either CAR or PXR, rather it functions as a selective inducer of CAR expression and increases CYP3A4 through a noncanonical CAR-related mechanism.
抑制胰岛素样生长因子-1 受体 (IGF-1R) 信号转导代表了癌症治疗的一种有吸引力的治疗策略。然而,第一代 IGF-1R 抑制剂 (R)-4-(3-(3-氯苯基)-3-羟基丙基)-3-(4-甲基-6-吗啉-1H-苯并[d]咪唑-2-基)吡啶-2(1H)-酮 (BMS-536924) 与孕烷 X 受体 (PXR; NR1I2) 反式激活介导的强烈 CYP3A4 诱导有关。基于结构的活性修饰导致合成了 4-(1-(2-(4-((2-(4-氯-1H-吡唑-1-基)乙基)氨基)-2-氧代-1,2-二氢吡啶-3-基)-4-甲基-1H-苯并[d]咪唑-6-基)哌啶-4-基)哌嗪-1-羧酸酯 (BMS-665351),其没有 PXR 活性,同时保持抑制 IGF-1R 的能力。然而,BMS-665351 在人原代肝细胞 (HPH) 中显着诱导 CYP3A4 的表达。在这里,我们报告了 BMS-665351 介导的 CYP3A4 诱导的一种新型非经典的组成型雄烷受体 (CAR; NR1I3) 相关途径。BMS-665351 处理导致 HPH 和 HepG2 细胞中 CYP3A4 的显着诱导,但在基于细胞的报告测定中未能激活 PXR 或 CAR。此外,在诱导 CYP3A4 表达的浓度下,BMS-665351 无法将人 CAR 从细胞质易位到 HPH 的细胞核,这是 CAR 激活的初始步骤。然而,定量聚合酶链反应分析表明,BMS-665351 显着增强了 CAR-但不是 PXR-转染的 HepG2 和 Huh7 细胞中 CYP3A4 的表达。值得注意的是,BMS-665351 在所有测试的肝细胞系统中均选择性诱导 CAR 的表达而不是 PXR。在 HPH 中,BMS-665351 与 CAR 但不是 PXR 的典型激活剂共同处理可观察到 CYP3A4 的协同诱导。总之,我们的结果表明,BMS-665351 介导的 CYP3A4 诱导是 CAR 依赖性的,但 BMS-665351 本身不是 CAR 或 PXR 的典型激活剂,而是作为 CAR 表达的选择性诱导剂,并通过非典型的 CAR 相关机制增加 CYP3A4。