Dolai Narayan, Kumar Ashish, Islam Aminul, Haldar Pallab K
a Department of Pharmaceutical Technology , Jadavpur University , Kolkata 700032 , India.
b Chemistry Division, CSIR-Indian Institute of Chemical Biology , Kolkata 700032 , India.
Nat Prod Res. 2016;30(4):482-5. doi: 10.1080/14786419.2015.1023201. Epub 2015 Mar 19.
β-Sitosterol glucoside (BSSG) is a natural biologically active substance isolated from the Castanopsis indica leaves. This study explored the apoptogenic mechanistic studies of BSSG against Ehrlich's ascites carcinoma (EAC) treated mice through morphological study, comet assay, flow cytometry (FACS) and Western blotting assay method. AO/EB staining and FACS analysis showed that BSSG possessed apoptosis induction activities on EAC cells. Dose dependent induction of DNA damage was observed after BSSG treatment. Increase the expression of apoptotic protein p53 and p21 in EAC, multiple downstream factors contributing to apoptosis pathway. The increase of caspase-9 and caspase-3 activities revealed that caspase was a key mediator of the apoptotic pathway induced by BSSG, and up-regulation of Bax and down-regulation of anti-apoptotic protein Bcl-2 resulted in the decrease of Bcl-2/Bax ratio. Owing to the combination of significant antitumour activity by inducing apoptosis, BSSG holds the promise of being an interesting chemo-preventive agent active in cancer therapy.
β-谷甾醇葡萄糖苷(BSSG)是从印度锥栗树叶中分离出的一种天然生物活性物质。本研究通过形态学研究、彗星试验、流式细胞术(FACS)和蛋白质免疫印迹分析方法,探讨了BSSG对艾氏腹水癌(EAC)处理小鼠的凋亡机制研究。AO/EB染色和FACS分析表明,BSSG对EAC细胞具有凋亡诱导活性。BSSG处理后观察到剂量依赖性的DNA损伤诱导。EAC中凋亡蛋白p53和p21表达增加,多个下游因子参与凋亡途径。caspase-9和caspase-3活性的增加表明,caspase是BSSG诱导凋亡途径的关键介质,促凋亡蛋白Bax的上调和抗凋亡蛋白Bcl-2的下调导致Bcl-2/Bax比值降低。由于BSSG通过诱导凋亡具有显著的抗肿瘤活性,它有望成为一种在癌症治疗中具有活性的有趣的化学预防剂。