Bergenin, Isolated Compound from Crassula ovata Plant, Its Role as  Synergistic Effect With Docetaxel Against Prostatic Cancer (PC-3) Cell Lines

Hawraa Kareem Lifta, Enas Jawad Kadhim
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Abstract

The synergistic effect of the bergenin compound, derived from the Crassula ovata plant, and the docetaxel drug in vitro cell line was assessed in this study. The bergenin compound was extracted using a Soxhlet device and 85% ethanol, then was identified and isolated using a high-performance liquid chromatograph. Docetaxel is regarded as a potent chemotherapy treatment that was licensed in 1996 to treat a variety of cancers, including prostate cancer, by preventing microtubular depolymerization and reducing the impact of bcl-2 and bcl-xL gene expression. It is considered one of the most effective chemotherapy treatment for prostatic cancer. However, it has adverse effects, including febrile neutropenia or myelosuppression. This study aim to combine the docetaxel with new natural compound as there is no previous study on combination between the docetaxel and bergenin to reduce the therapeutic dose as much as possible and obtain same therapeutic effect .The results demonstrated that bergenin exhibits a good synergistic effect against prostatic cancer with IC50 equal to 26 as a phenolic compound that can induce G0/G1 cell cycle arrest, enhance the expression of Bax, decrease the expression of Bcl-2, and inhibit the PI3K/AKT/mTOR pathway. As revealed by the results, the inhibition effect of the combination (bergenin and IC50 docetaxel equal to 89,8) was 64, compared to an inhibition effect of 62 for 100 mcg of docetaxel and the data obtained were analyzed by one-way ANOVA with a significance level of "p < 0.05" .
龙苏植物分离化合物卑尔根素与多西他赛对前列腺癌(PC-3)细胞系的协同作用
本研究评价了从茄叶植物中提取的卑尔根素化合物与多西紫杉醇药物在体外细胞系中的协同作用。采用索氏装置和85%乙醇提取,高效液相色谱分离鉴定。多西他赛被认为是一种有效的化疗药物,1996年被批准用于治疗多种癌症,包括前列腺癌,通过防止微管解聚和减少bcl-2和bcl-xL基因表达的影响。它被认为是治疗前列腺癌最有效的化疗方法之一。然而,它有副作用,包括发热性中性粒细胞减少或骨髓抑制。本研究旨在将多西紫杉醇与新的天然化合物联合使用,以尽可能减少治疗剂量,获得相同的治疗效果,目前尚无多西紫杉醇与茄子素联合使用的研究。结果表明,卑尔根素作为一种能够诱导G0/G1细胞周期阻滞、增强Bax表达、降低Bcl-2表达、抑制PI3K/AKT/mTOR通路的酚类化合物,对前列腺癌具有良好的协同作用,IC50为26。结果显示,与100 mcg多西他赛的抑制效应62相比,联合用药(卑尔根素与IC50多西他赛= 89,8)的抑制效应为64,所得数据采用单因素方差分析,显著性水平为“p < 0.05”。
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