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普朗尼克嵌段共聚物放射增敏活性的临床前评价。

Preclinical evaluation of radiosensitizing activity of Pluronic block copolymers.

机构信息

Department of Radiology, Case Western Reserve University , Cleveland, Ohio , USA.

出版信息

Int J Radiat Biol. 2013 Oct;89(10):801-12. doi: 10.3109/09553002.2013.800246. Epub 2013 Jun 3.

Abstract

PURPOSE

Pluronic block copolymers are non-ionic surfactants with demonstrated sensitizing activity in chemotherapy and hyperthermia in various tumor cell lines. In the current study we investigated the potential activity of Pluronic as a radiosensitizing agent.

MATERIALS AND METHODS

As a possible mechanism, the effect of Pluronic on Hsp70 and Hsp90 was examined. Gli36 human glioma cells were treated with radiation alone as well as with a combination treatment of Pluronic and radiation.

RESULTS

Clonogenic cell survival assays show that Pluronic has an elevated effect on radiosensitization (50% high, p < 0.01), even with radiation doses as low as 2 Gy. The Hsp90 level was reduced 24 h after the combined treatment in both in vitro and in vivo. Similarly, Hsp70 levels were also decreased 24 h post treatment. When Gli36 cells were exposed to Pluronic before and during irradiation, DNA DSB: double-strand breaks repair was reduced, and elevated apoptosis was also seen in tumor xenografts.

CONCLUSION

Data suggest the potential use of L10 as a radiosensitizer. While the mechanism of sensitization requires additional investigation, the presented results indicate that the effect may be due, in part, to a decrease in Hsp90 and 70 levels and increased DNA damage.

摘要

目的

普朗尼克嵌段共聚物是一种非离子表面活性剂,已在多种肿瘤细胞系的化疗和热疗中表现出致敏活性。在目前的研究中,我们研究了普朗尼克作为放射增敏剂的潜在活性。

材料和方法

作为一种可能的机制,研究了普朗尼克对热休克蛋白 70(Hsp70)和热休克蛋白 90(Hsp90)的影响。用单独的辐射以及普朗尼克与辐射的联合处理来处理Gli36 人神经胶质瘤细胞。

结果

集落形成细胞存活实验表明,普朗尼克对放射增敏作用具有升高的作用(50%高,p < 0.01),即使辐射剂量低至 2 Gy。联合治疗后 24 小时,体外和体内的 Hsp90 水平均降低。同样,Hsp70 水平在治疗后 24 小时也降低。当Gli36 细胞在照射前和照射期间暴露于普朗尼克时,DNA DSB:双链断裂修复减少,并且肿瘤异种移植物中也观察到凋亡增加。

结论

数据表明 L10 有作为放射增敏剂的潜力。虽然增敏的机制需要进一步研究,但目前的结果表明,这种效应可能部分是由于 Hsp90 和 70 水平的降低以及 DNA 损伤的增加所致。

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