首页> 外文期刊>The Journal of Pharmacology and Experimental Therapeutics: Official Publication of the American Society for Pharmacology and Experimental Therapeutics >Efflux Transporters at the Blood-Brain Barrier Limit Delivery and Efficacy of Cyclin-Dependent Kinase 4/6 Inhibitor Palbociclib (PD-0332991) in an Orthotopic Brain Tumor Model
【24h】

Efflux Transporters at the Blood-Brain Barrier Limit Delivery and Efficacy of Cyclin-Dependent Kinase 4/6 Inhibitor Palbociclib (PD-0332991) in an Orthotopic Brain Tumor Model

机译:在原位脑肿瘤模型中血脑屏障的外向转运蛋白转运和细胞周期蛋白依赖性激酶4/6抑制剂Palbociclib(PD-0332991)的功效。

获取原文
获取原文并翻译 | 示例
           

摘要

6-Acetyl-8-cyclopentyl-5-methyl-2-([5-(piperazin-1-yl)pyridin-2yl] amino)pyrido(2,3-d)pyrimidin-7(8H)-one [palbociclib (PD-0332991)] is a cyclin-dependent kinase 4/6 inhibitor approved for the treatment of metastatic breast cancer and is currently undergoing clinical trials for many solid tumors. Glioblastoma (GBM) is the most common primary brain tumor in adults and has limited treatment options. The cyclin-dependent kinase 4/6 pathway is commonly dysregulated in GBM and is a promising target in treating this devastating disease. The blood-brain barrier (BBB) limits the delivery of drugs to invasive regions of GBM, where the efflux transporters P-glycoprotein and breast cancer resistance protein can prevent treatments from reaching the tumor. The purpose of this study was to examine the mechanisms limiting the effectiveness of palbociclib therapy in an orthotopic xenograft model. The in vitro intracellular accumulation results demonstrated that palbociclib is a substrate for both P-glycoprotein and breast cancer resistance protein. In vivo studies in transgenic mice confirmed that efflux transport is responsible for the limited brain distribution of palbociclib. There was an similar to 115-fold increase in brain exposure at steady state in the transporter deficient mice when compared with wild-type mice, and the efflux inhibitor elacridar significantly increased palbociclib brain distribution. Efficacy studies demonstrated that palbociclib is an effective therapy when GBM22 tumor cells are implanted in the flank, but ineffective in an orthotopic (intracranial) model. Moreover, doses designed to mimic brain exposure were ineffective in treating flank tumors. These results demonstrate that efflux transport in the BBB is involved in limiting the brain distribution of palbociclib and this has critical implications in determining effective dosing regimens of palbociclib therapy in the treatment of brain tumors.
机译:6-乙酰基-8-环戊基-5-甲基-2-([5-(哌嗪-1-基)吡啶-2-基]氨基)吡啶基(2,3-d)嘧啶-7(8H)-一个[palbociclib( PD-0332991)]是一种细胞周期蛋白依赖性激酶4/6抑制剂,已被批准用于治疗转移性乳腺癌,目前正在针对许多实体瘤进行临床试验。胶质母细胞瘤(GBM)是成人中最常见的原发性脑肿瘤,治疗选择有限。细胞周期蛋白依赖性激酶4/6通路在GBM中通常失调,并且是治疗这种破坏性疾病的有希望的靶标。血脑屏障(BBB)限制了药物向GBM的侵入区域的输送,在该区域,外排转运蛋白P-糖蛋白和乳腺癌抗性蛋白可以阻止治疗药物到达肿瘤。这项研究的目的是检查在原位异种移植模型中限制palbociclib治疗有效性的机制。体外细胞内积累结果表明,palbociclib是P-糖蛋白和乳腺癌抗性蛋白的底物。对转基因小鼠的体内研究证实,外排转运是造成palbociclib大脑分布受限的原因。与野生型小鼠相比,转运缺陷型小鼠在稳态下的大脑暴露增加了约115倍,外排抑制剂埃拉西达显着增加了palbociclib的大脑分布。功效研究表明,当将GBM22肿瘤细胞植入侧面时,palbociclib是一种有效的疗法,但在原位(颅内)模型中无效。而且,模拟大脑暴露的剂量在治疗胁腹肿瘤方面无效。这些结果表明,血脑屏障中的外排转运参与限制palbociclib的脑部分布,这对于确定palbociclib治疗脑肿瘤的有效给药方案具有关键意义。

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号