Impact of Honeybee Venom Melittin on Cell Viability of Different Prostate Cancer Lineages

R. Khalikov, D. D. Gromenko, S. Galimova, K. Danilko, I. D. Gromenko, S. Galimov, P. Litvitsky
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Abstract

Background. Melittin is a major constituent of honeybee venom and comprises a water-soluble surfactant peptide with cytolytic effects potentially applicable in anticancer therapy. We evaluated the impact of melittin from Bashkir honeybee (Apis mellifera mellifera L.) venom on cell viability of various prostate cancer lineages.Materials and methods. MTT assays with cell viability index estimation were used to evaluate the effect of melittin on cell proliferation in various-grade malignancy prostate cancer (PC) lineages, LNCaP, PC-3 and DU145.Results and discussion. Lineage DU145 revealed a low sensitivity to melittin, because a relatively high peptide concentration of 10 μg/mL had a suppressive effect on its proliferation. With PC-3 cells, a 0.1 μg/mL concentration suppressed proliferation significantly to 46.15 %, while melittin at a 10 μg/mL dose had a cytolytic effect on most cells (4.27 % viability). LNCaP cells experienced the lowest toxicity at 10 μg/mL melittin compared to PC-3 and DU145 lineages. The LNCaP, PC-3 and DU145 PC lineages demonstrated suppressed proliferation at melittin levels 0.01–100 μg/mL.Conclusion. The study reveals a significant reduction of the PC lineages viability at a minimal melittin concentration of 0.01 μg/mL, which indicates a high cytolytic activity of this peptide and renders it a candidate agent in antitumour therapy.
蜂毒蜂毒肽对不同前列腺癌癌症系细胞活力的影响
背景蜂毒肽是蜂毒的主要成分,包括一种水溶性表面活性剂肽,具有潜在的抗癌作用。我们评估了Bashkir蜜蜂(Apis mellifera mellifera L.)毒素中的蜂毒肽对各种前列腺癌症谱系细胞活力的影响。材料和方法。采用MTT法和细胞活力指数测定法,评价蜂毒肽对不同粒径恶性前列腺癌症(PC)、LNCaP、PC-3和DU145细胞增殖的影响。结果与讨论。品系DU145对蜂毒肽的敏感性较低,因为相对较高的肽浓度(10μg/mL)对其增殖具有抑制作用。对于PC-3细胞,0.1μg/mL浓度显著抑制增殖至46.15%,而10μg/mL剂量的蜂毒肽对大多数细胞具有细胞溶解作用(4.27%的活力)。与PC-3和DU145谱系相比,LNCaP细胞在10μg/mL蜂毒肽下的毒性最低。LNCaP、PC-3和DU145 PC谱系在蜂毒肽水平为0.01–100μg/mL时表现出抑制增殖的作用。结论。研究表明,在最低蜂毒肽浓度为0.01μg/mL的情况下,PC谱系的活力显著降低,这表明该肽具有较高的细胞溶解活性,并使其成为抗肿瘤治疗的候选药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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审稿时长
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