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GSK461364A a Polo-Like Kinase-1 Inhibitor Encapsulated in Polymeric Nanoparticles for the Treatment of Glioblastoma Multiforme (GBM)

机译:GSK461364A一种包裹在聚合物纳米颗粒中的Polo样激酶1抑制剂用于治疗多形性胶质母细胞瘤(GBM)

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摘要

Glioblastoma Multiforme (GBM) is a common primary brain cancer with a poor prognosis and a median survival of less than 14 months. Current modes of treatment are associated with deleterious side effects that reduce the life span of the patients. Nanomedicine enables site-specific delivery of active pharmaceutical ingredients and facilitates entrapment inside the tumor. Polo-like kinase 1 (PLK-1) inhibitors have shown promising results in tumor cells. GSK461364A (GSK) is one such targeted inhibitor with reported toxicity issues in phase 1 clinical trials. We have demonstrated in our study that the action of GSK is time dependent across all concentrations. There is a distinct 15−20% decrease in cell viability via apoptosis in U87-MG cells dosed with GSK at low concentrations (within the nanomolar and lower micromolar range) compared to higher concentrations of the drug. Additionally, we have confirmed that PLGA-PEG nanoparticles (NPs) containing GSK have shown significant reduction in cell viability of tumor cells compared to their free equivalents. Thus, this polymeric nanoconstruct encapsulating GSK can be effective even at low concentrations and could improve the effectiveness of the drug while reducing side effects at the lower effective dose. This is the first study to report a PLK-1 inhibitor (GSK) encapsulated in a nanocarrier for cancer applications.
机译:多形胶质母细胞瘤(GBM)是一种常见的原发性脑癌,预后较差,中位生存期少于14个月。当前的治疗方式与有害的副作用有关,这些副作用减少了患者的寿命。纳米医学使活性药物成分能够定点递送,并促进肿瘤内部的包埋。马球样激酶1(PLK-1)抑制剂已在肿瘤细胞中显示出令人鼓舞的结果。 GSK461364A(GSK)是一种此类靶向抑制剂,在1期临床试验中报告了毒性问题。我们的研究表明,在所有浓度下,GSK的作用均与时间有关。与较高浓度的药物相比,在低浓度(在纳摩尔和较低微摩尔范围内)服用GSK的U87-MG细胞中,通过凋亡引起的细胞活力明显降低了15-20%。另外,我们已经证实,与它们的游离等同物相比,含有GSK的PLGA-PEG纳米颗粒(NP)已显示出肿瘤细胞的细胞活力显着降低。因此,这种包封GSK的聚合物纳米构造体即使在低浓度下也可以是有效的,并且可以提高药物的效力,同时在较低的有效剂量下减少副作用。这是第一个报道PLK-1抑制剂(GSK)封装在纳米载体中用于癌症的研究。

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