Gowda Raghavendra, Kardos Gregory, Sharma Arati, Singh Sanjay, Robertson Gavin P
Department of Pharmacology, The Pennsylvania State University College of Medicine, Hershey, Pennsylvania.
The Penn State Melanoma and Skin Cancer Center, The Pennsylvania State University College of Medicine, Hershey, Pennsylvania.
Mol Cancer Ther. 2017 Mar;16(3):440-452. doi: 10.1158/1535-7163.MCT-16-0285. Epub 2016 Dec 21.
Using multiple drugs to kill cancer cells can decrease drug resistance development. However, this approach is frequently limited by the bioavailability and toxicity of the combined agents and delivery at ratios to specific locations that synergistically kill cancer cells. Loading the individual agents into a nanoparticle that releases the drugs at synergizing ratios at a single location is one approach to resolve this concern. Celecoxib and plumbagin are two drugs that were identified from a screen to synergistically kill melanoma cells compared with normal cells. Combined use of these agents by traditional approaches was not possible due to poor bioavailability and toxicologic concerns. This study details the development of a nanoliposomal-based agent containing celecoxib and plumbagin, called CelePlum-777, which is stable and releases these drugs at an optimal ratio for maximal synergistic killing efficacy. CelePlum-777 was more effective at killing melanoma than normal cells and inhibited xenograft melanoma tumor growth by up to 72% without apparent toxicity. Mechanistically, the drug combination in CelePlum-777 led to enhanced inhibition of melanoma cell proliferation mediated by decreasing levels of key cyclins important for cancer cell proliferation and survival, which was not observed with the individual agents. Thus, a novel nanoparticle-based drug has been developed containing celecoxib and plumbagin that lacks toxicity and delivers the agents at a synergistically killing drug ratio to kill cancer cells. .
使用多种药物杀死癌细胞可以降低耐药性的产生。然而,这种方法常常受到联合用药的生物利用度、毒性以及以协同杀死癌细胞的比例将药物递送至特定部位的限制。将每种药物载入纳米颗粒中,使其在单一部位以协同比例释放药物,是解决这一问题的一种方法。塞来昔布和白花丹醌是从筛选中确定的两种药物,与正常细胞相比,它们能协同杀死黑色素瘤细胞。由于生物利用度差和毒理学问题,无法通过传统方法联合使用这些药物。本研究详细介绍了一种基于纳米脂质体的制剂CelePlum-777的研发过程,该制剂含有塞来昔布和白花丹醌,稳定且能以最佳比例释放这些药物,以实现最大的协同杀伤效果。CelePlum-777在杀死黑色素瘤细胞方面比正常细胞更有效,并且能抑制异种移植黑色素瘤肿瘤生长达72%,且无明显毒性。从机制上讲,CelePlum-777中的药物组合通过降低对癌细胞增殖和存活至关重要的关键细胞周期蛋白水平,增强了对黑色素瘤细胞增殖的抑制作用,而单一药物则未观察到这种现象。因此,已研发出一种新型的基于纳米颗粒的药物,其含有塞来昔布和白花丹醌,无毒且能以协同杀伤药物比例递送药物以杀死癌细胞。