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

机译:基于纳米粒子的Celecoxib和朱锐素,用于黑素瘤的协同疗法

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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 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. (C)2016 AACR.
机译:使用多种药物杀死癌细胞可以降低耐药性发育。然而,这种方法经常受组合剂的生物利用度和毒性的限制,并以比例的递送到协同杀死癌细胞的特定位置。将个体剂加载到纳米颗粒中,该纳米颗粒在单个位置在协同率下释放药物是解决这一问题的一种方法。 Celecoxib和肠果素是两种药物,其从筛选中鉴定到与正常细胞相比协同杀死黑色素瘤细胞的药物。由于生物利用度差和毒理学担心,不可能通过传统方法使用传统方法的结合使用。该研究细节了含有塞克昔布和肠果素的纳米脂素的药剂的发展,称为Celeplum-777,其以最大的比例稳定并释放这些药物以获得最大的协同杀伤效果。 Celeplum-777在杀死黑色素瘤比正常细胞更有效,并且抑制异种移植的黑色素瘤肿瘤的生长达72%,而无表观毒性。机械地,Celeplum-777中的药物组合导致通过减少对癌细胞增殖和存活的关键细胞周期胰蛋白酶水平介导的对黑色素瘤细胞增殖的抑制性,这未与个体药物观察到。因此,已经开发了一种新的纳米颗粒基药物,其含有塞克西布和肠道蛋白,其缺乏毒性,并以协同杀死药物比例递送药物以杀死癌细胞。 (c)2016 AACR。

著录项

  • 来源
    《Molecular cancer therapeutics》 |2017年第3期|共13页
  • 作者单位

    Penn State Univ Dept Pharmacol Coll Med 500 Univ Dr Hershey PA 17033 USA;

    Penn State Univ Dept Pharmacol Coll Med 500 Univ Dr Hershey PA 17033 USA;

    Penn State Univ Dept Pharmacol Coll Med 500 Univ Dr Hershey PA 17033 USA;

    Penn State Univ Dept Pharmacol Coll Med 500 Univ Dr Hershey PA 17033 USA;

    Penn State Univ Dept Pharmacol Coll Med 500 Univ Dr Hershey PA 17033 USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 肿瘤学;
  • 关键词

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