Inst Neurophysiopathol (INP), CNRS, Aix-Marseille Université, 13385 Marseille, France.
Department of Natural Sciences, Lebanese American University, Byblos P.O. Box 36, Lebanon.
Molecules. 2024 Aug 21;29(16):3950. doi: 10.3390/molecules29163950.
Glioblastoma multiforme (GBM) is a highly aggressive and fatal primary brain tumor. The resistance of GBM to conventional treatments is attributed to factors such as the blood-brain barrier, tumor heterogeneity, and treatment-resistant stem cells. Current therapeutic efforts show limited survival benefits, emphasizing the urgent need for novel treatments. In this context, natural anti-cancer extracts and especially animal venoms have garnered attention for their potential therapeutic benefits. Bee venom in general and that of the Middle Eastern bee, in particular, has been shown to have cytotoxic effects on various cancer cell types, but not glioblastoma. Therefore, this study aimed to explore the potential of venom as a selective anti-cancer agent for glioblastoma through in vitro and in vivo studies. Our results revealed a strong cytotoxic effect of venom on U87 glioblastoma cells, with an IC50 of 14.32 µg/mL using the MTT test and an IC50 of 7.49 µg/mL using the LDH test. Cells treated with the bee venom became permeable to propidium iodide without showing any signs of early apoptosis, suggesting compromised membrane integrity but not early apoptosis. In these cells, poly (ADP-ribose) polymerase (PARP) underwent proteolytic cleavage similar to that seen in necrosis. Subsequent in vivo investigations demonstrated a significant reduction in the number of U87 cells in mice following bee venom injection, accompanied by a significant increase in cells expressing caspase-3, suggesting the occurrence of cellular apoptosis. These findings highlight the potential of venom as a therapeutically useful tool in the search for new drug candidates against glioblastoma and give insights into the molecular mechanism through which the venom acts on cancer cells.
胶质母细胞瘤(GBM)是一种高度侵袭性和致命性的原发性脑肿瘤。GBM 对传统治疗的耐药性归因于血脑屏障、肿瘤异质性和耐药性干细胞等因素。目前的治疗方法显示出有限的生存获益,这强调了对新治疗方法的迫切需求。在这种情况下,天然抗癌提取物,特别是动物毒液,因其潜在的治疗益处而受到关注。一般来说,蜜蜂毒液,特别是中东蜜蜂的毒液,已被证明对各种癌细胞类型具有细胞毒性作用,但对胶质母细胞瘤没有作用。因此,这项研究旨在通过体外和体内研究探索 毒液作为胶质母细胞瘤选择性抗癌剂的潜力。我们的结果显示,毒液对 U87 胶质母细胞瘤细胞具有强烈的细胞毒性作用,MTT 试验的 IC50 为 14.32 µg/mL,LDH 试验的 IC50 为 7.49 µg/mL。用蜜蜂毒液处理的细胞对碘化丙啶变得具有渗透性,而没有显示出任何早期凋亡的迹象,这表明膜完整性受损,但不是早期凋亡。在这些细胞中,多聚(ADP-核糖)聚合酶(PARP)经历了与坏死相似的蛋白水解切割。随后的体内研究表明,在注射蜜蜂毒液后,小鼠中 U87 细胞的数量显著减少,同时表达 caspase-3 的细胞数量显著增加,这表明发生了细胞凋亡。这些发现突出了 毒液作为治疗上有用的工具在寻找新的候选药物治疗胶质母细胞瘤方面的潜力,并深入了解毒液作用于癌细胞的分子机制。