Fathalizadeh J, Bagheri V, Khorramdelazad H, Kazemi Arababadi M, Jafarzadeh A, Mirzaei M R, Shamsizadeh A, Hajizadeh M R
Rafsanjan University of Medical Sciences Immunology of Infectious Diseases Research Center Rafsanjan Iran.
Rafsanjan University of Medical Sciences Molecular Medicine Research Center Rafsanjan Iran.
Cell Mol Biol (Noisy-le-grand). 2015 Nov 30;61(7):128-34.
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 ~ 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.
几种重要的黄连木属物种,如阿月浑子,传统上被用于治疗多种疾病(例如,与肝脏相关的疾病)。对开心果壳的药理学方面的研究相对较少。因此,本研究旨在调查开心果玫瑰色外壳(PRH)提取物是否对HepG2肝癌细胞系产生凋亡影响。为了评估提取物处理后的细胞活力和凋亡情况,分别进行了MTT试验和膜联蛋白V-荧光素/碘化丙啶(PI)双重染色。此外,使用人类凋亡PCR阵列确定了提取物诱导凋亡的分子机制。我们的研究结果表明,PRH提取物处理以剂量依赖性方式降低细胞活力(IC50约为0.3 mg/ml)。流式细胞仪分析显示,该提取物显著诱导HepG2细胞凋亡。此外,定量PCR阵列结果表明,大量属于TNF、BCL2、IAP、TRAF和半胱天冬酶家族的凋亡相关基因受到调控。我们观察到与外源性和内源性凋亡信号通路相关的促凋亡和抗凋亡基因的表达发生了改变。这些结果表明,PRH水提取物通过对HepG2细胞的细胞毒性和凋亡诱导作用具有凋亡活性。