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Induction of apoptosis by pistachio (Pistacia vera L.) hull extract and its molecular mechanisms of action in human hepatoma cell line HepG2

机译:开心果(Pistacia vera L.)壳提取物诱导人肝癌细胞HepG2凋亡及其分子机制

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摘要

Several important Pistacia species such as P. vera have been traditionally used for treating a wide range of diseases (for instance, liver-related disorders). There is a relative lack of research into pharmacological aspects of pistachio hull. Hence, this study was aimed at investigating whether pistachio rosy hull (PRH) extract exerts apoptotic impacts on HepG2 liver cancer cell line. In order to evaluate cell viability and apoptosis in response to treatment with the extract, MTT assay and Annexin-V-fluorescein/propidium iodide (PI) double staining were performed, respectively. Moreover, molecular mechanism of apoptosis induced by the extract was determined using human apoptosis PCR array. Our findings showed that PRH extract treatment reduced cell viability (IC50 similar to 0.3 mg/ml) in a dose-dependent manner. Flow cytometric analysis revealed that the extract significantly induced apoptosis in HepG2 cells. In addition, quantitative PCR array results demonstrated the regulation of a considerable number of apoptosis-related genes belonging to the TNF, BCL2, IAP, TRAF, and caspase families. We observed altered expression of both pro-apoptotic and anti-apoptotic genes associated with the extrinsic and intrinsic apoptosis signaling pathways. These results suggest that the aqueous extract of PRH possesses apoptotic activity through cytotoxic and apoptosis-inducing effects on HepG2 cells.
机译:传统上已经使用了几种重要的黄连木种,例如维拉假单胞菌(P. vera)来治疗多种疾病(例如,与肝脏有关的疾病)。开心果壳的药理学方面相对缺乏研究。因此,本研究旨在调查开心果玫瑰果壳(PRH)提取物是否对HepG2肝癌细胞系产生凋亡影响。为了评估响应提取物处理的细胞活力和凋亡,分别进行了MTT测定和膜联蛋白-V-荧光素/碘化丙啶(PI)双重染色。此外,使用人凋亡PCR阵列确定了提取物诱导的凋亡的分子机制。我们的发现表明PRH提取物治疗以剂量依赖的方式降低了细胞活力(IC50类似于0.3 mg / ml)。流式细胞仪分析表明提取物显着诱导HepG2细胞凋亡。另外,定量PCR阵列结果证明了对与TNF,BCL2,IAP,TRAF和胱天蛋白酶家族有关的许多凋亡相关基因的调控。我们观察到与外部和固有凋亡信号通路相关的促凋亡和抗凋亡基因的表达改变。这些结果表明PRH的水提取物通过对HepG2细胞的细胞毒性和细胞凋亡诱导作用而具有凋亡活性。

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