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Nanoparticle-based Celecoxib and Plumbagin for the Synergistic Treatment of Melanoma

机译:基于纳米颗粒的塞来昔布和Plumbagin协同治疗黑色素瘤。

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摘要

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 the 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 to normal cells. Combined use of these agents by traditional approaches was not possible due to poor bioavailability and toxicological 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 cyclin 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 deliverers the agents at a synergistically killing drug ratio to kill cancer cells.
机译:使用多种药物杀死癌细胞可以降低耐药性的发展。然而,这种方法经常受到联合药剂的生物利用度和毒性以及以协同作用杀死癌细胞的特定位置的比例递送的限制。将单个药物加载到纳米颗粒中,该纳米颗粒可以在单个位置以协同作用的比例释放药物,这是解决此问题的一种方法。 Celecoxib和Plumbagin是从筛选中鉴定出的与正常细胞相比可协同杀死黑色素瘤细胞的两种药物。由于不良的生物利用度和毒理学方面的考虑,不可能通过传统方法联合使用这些药物。这项研究详细介绍了包含Celecoxib和Plumbagin的纳米脂质体药物CelePlum-777的开发,该药物稳定并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在杀死黑色素瘤方面比正常细胞更有效,并且最多可将异种移植黑色素瘤肿瘤抑制72%,而无明显毒性。从机理上讲,CelePlum-777中的药物组合导致对黑色素瘤细胞增殖的抑制作用增强,该抑制作用是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的水平介导的,而在单个药物中未观察到。因此,已经开发了一种新型的基于纳米颗粒的药物,该药物含有塞来昔布和Plumbagin,它们没有毒性,并且以协同杀伤药物的比例递送药剂以杀死癌细胞。

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