Berberine Synergizes with Cisplatin via Inducing Apoptosis on A549 non-Small Cell Lung Cancer Cells

IF 0.3 Q3 MEDICINE, GENERAL & INTERNAL
Merve Becit-Kızılkaya, Şeyma Öncü, Serkan Şen, Sefa Çelik
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Abstract

Objective: Lung cancer is the most common cause of morbidity and mortality. Platinum-based chemotherapy, which is the primary line of treatment, offers limited benefit due to drug resistance and side effects. Berberine (BBR), which is characterised by its potent and safe anticancer activity, represents a promising combination option in chemotherapy. To overcome the limitations in lung cancer chemotherapy, we investigated whether BBR and cisplatin (CIS) exert synergistic effects on non-small cell lung cancer cell line (A549) based on cytotoxicity and apoptotic response markers. Methods: The potential cytotoxic effects of the combination treatment were evaluated using the MTT and Chou-Talalay methods. Elisa assays were also performed to measure the levels of the pro-apoptotic protein Bax and the effector protein caspase (Cas)-3. Results: The results showed that BBR alone reduced A549 cell viability in a dose-dependent manner and synergized with CIS (CI =0.34±0.05 at IC50 concentrations). Elisa results showed that the combined treatment (both at IC50 concentrations) modulated apoptotic signalling pathways in A549 cells. Bax and Cas3 protein levels were dramatically enhanced in A549 cells treated with CIS +BBR compared to control (0.5% DMSO) (p < 0.001). Conclusion: Our results suggest that BBR can synergistically enhance the therapeutic effect of CIS in A549 cells. The potential therapeutic efficacy of BBR as part of a combination in current chemotherapy should be supported by in-depth research and clinical studies on the molecular mechanisms associated with cancer.
小檗碱与顺铂协同作用诱导A549非小细胞肺癌细胞凋亡
目的:肺癌是最常见的发病和死亡原因。以铂类药物为基础的化疗是主要的治疗方法,由于耐药和副作用,疗效有限。小檗碱(BBR),其特点是其有效和安全的抗癌活性,是一个有前途的联合化疗选择。为了克服肺癌化疗的局限性,我们基于细胞毒性和凋亡反应标志物,研究了BBR和顺铂(CIS)对非小细胞肺癌细胞系(A549)是否具有协同作用。方法:采用MTT法和Chou-Talalay法评价联合用药的潜在细胞毒作用。Elisa法检测促凋亡蛋白Bax和效应蛋白caspase (Cas)-3的水平。结果:单用BBR对A549细胞的活性降低呈剂量依赖性,且与CIS有协同作用(IC50浓度下CI =0.34±0.05)。Elisa结果显示,两种浓度的IC50联合处理可调节A549细胞的凋亡信号通路。与对照组(0.5% DMSO)相比,CIS +BBR处理的A549细胞中Bax和Cas3蛋白水平显著提高(p < 0.001)。结论:BBR可协同增强CIS对A549细胞的治疗作用。在目前的化疗中,BBR作为联合治疗的一部分,其潜在的治疗效果需要深入的研究和与癌症相关的分子机制的临床研究来支持。
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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来源期刊
European Journal of Therapeutics
European Journal of Therapeutics MEDICINE, GENERAL & INTERNAL-
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