狼蛛毒液联合替莫唑胺对人胶质母细胞瘤细胞的体外抗肿瘤作用。

Umit Kocaman, Fatih Collu, Berrin Tugrul, Mesut Mete, Emre Cavusoglu, Beyhan Gurcu, Ibrahim Tuglu
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引用次数: 0

摘要

目的:探讨含狼蛛毒液的顺势疗法药物Tarantula Logoplex®(TL)单独或联合替莫唑胺(TMZ)对T98G胶质母细胞瘤细胞系的细胞毒性、细胞迁移、一氧化氮合酶(NOS)水平以及介导这种细胞毒性作用的程序性细胞死亡途径类型的影响。材料与方法:采用3-(4,5-二甲基噻唑-2)-2.5-二苯基溴化四氮唑(MTT)法分析细胞毒性作用,Annexin V-FITC/PI流式细胞术分析细胞凋亡,单anansylcadaverine染色法检测细胞自噬,四乙基苯并咪唑基碘化碳氰胺(JC-1)染色法检测线粒体膜电位,划痕试验分析细胞迁移。采用免疫荧光(IF)和western blot分析eNOS、iNOS和LC3蛋白水平。对结果进行比较和统计学评价。结果:Annexin V-FITC/PI流式细胞术显示,联合给药的细胞毒性较高,主要通过细胞凋亡产生(37.57%)。根据JC-1分析,凋亡效应可能来源于线粒体。荧光强度从强到弱依次为对照> TL >联合> TMZ,对照TL联合> TMZ,对照TL联合> TMZ。Western blotting结果显示,tlic25组eNOS和iNOS蛋白密度最高,tmzic50组LC3蛋白密度最高。结论:TL和TMZ联合给药可对T98G胶质母细胞瘤细胞产生明显的细胞毒性作用,其作用机制可能是细胞凋亡。TL可能起到增强常规治疗药物对胶质母细胞瘤疗效的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In Vitro Antitumoral Effect of Tarantula Venom Combined with Temozolomide in Human Glioblastoma Cells.

Aim: To investigate the effect of 48-hour (h) administration of Tarantula Logoplex® (TL), a homeopathic medical product containing Tarantula cubensis venom, alone and in combination with temozolomide (TMZ) on T98G glioblastoma cell line with regard to cytotoxicity, cell migration, nitric oxide synthase (NOS) level, and the type of programmed cell death pathway that mediates this cytotoxic effect.

Material and methods: Cytotoxic effect was analyzed using the 3-(4,5-dimethylthiazolyl-2)-2.5-diphenyltetrazolium bromide (MTT) method, apoptosis was analyzed by Annexin V-FITC/PI flow cytometry, autophagic cell imaging was performed using the monodansylcadaverine staining method, mitochondrial membrane potential was evaluated using the tetraethylbenzimidazolylcarbocyanine iodide (JC-1) staining method, and cell migration was analyzed using the scratch test. The levels of eNOS, iNOS, and LC3 proteins were evaluated using immunofluorescence (IF) and western blot analyses. Results were compared and statistically evaluated.

Results: Annexin V-FITC/PI flow cytometry revealed that the cytotoxicity of the combined administration was high and primarily (37.57%) occurred through apoptosis. According to JC-1 analysis, the apoptotic effect could have originated from mitochondria. Cell migration was lowest at the IC 50 dose of TL. The order of fluorescence intensity from the strongest to the weakest was control > TL > combination > TMZ for eNOS and control TL combination > TMZ for iNOS. Western blotting revealed the highest eNOS and iNOS protein density with TL IC 25 administration and the highest LC3 protein density with TMZ IC 50 administration.

Conclusion: Combined administration of TL and TMZ may exert a significant cytotoxic effect on T98G glioblastoma cells, which may occur through apoptosis. TL may play a role in augmenting the effect of conventional therapeutic drugs on glioblastoma.

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