Han Li, Guo Xiaojuan, Bian Hua, Yang Lei, Chen Zhong, Zang Wenhua, Yang Jingke
Zhang Zhongjing College of Chinese Medicine, Nanyang Institute of Technology, 80 Changjiang Road, Nanyang 473004, China.
College of Pharmaceutical Science, Soochow University, 199 Ren-ai Road, Suzhou 215123, China.
Evid Based Complement Alternat Med. 2016;2016:4651949. doi: 10.1155/2016/4651949. Epub 2016 May 18.
The aim of the study was to explore the possible mechanisms that Guizhi Fuling Wan (GFW) enhances the sensitivity of the SKOV3/DDP ovarian cancer cells and the resistant xenograft tumours to cisplatin. Rat medicated sera containing GFW were prepared by administering GFW to rats, and the primary bioactive constituents of the sera were gallic acid, paeonol, and paeoniflorin analysed by HPLC/QqQ MS. Cell counting kit-8 analysis was shown that coincubation of the sera with cisplatin/paclitaxel enhanced significantly the cytotoxic effect of cisplatin or paclitaxel in SKOV3/DDP cells. The presence of the rat medicated sera containing GFW resulted in an increase in rhodamine 123 accumulation by flow cytometric assays and a decrease in the protein levels of P-gp, phosphorylation of AKT at Ser473, and mTOR in a dose-dependent manner in SKOV3/DDP cells by western blot analysis, but the sera had no effect on the protein levels of PI3K p110α and total AKT. The low dose of GFW enhanced the anticancer efficacy of cisplatin and paclitaxel treatment in resistant SKOV3/DDP xenograft tumours. GFW could sensitize cisplatin-resistant SKOV3/DDP cells by inhibiting the protein level and function of P-gp, which may be medicated through inactivation of the PI3K/AKT/mTOR pathway.
本研究旨在探讨桂枝茯苓丸(GFW)增强SKOV3/DDP卵巢癌细胞和顺铂耐药异种移植瘤对顺铂敏感性的可能机制。通过给大鼠灌胃GFW制备含GFW的大鼠含药血清,采用HPLC/QqQ MS分析血清中的主要生物活性成分,为没食子酸、丹皮酚和芍药苷。细胞计数试剂盒-8分析表明,含药血清与顺铂/紫杉醇共同孵育可显著增强顺铂或紫杉醇对SKOV3/DDP细胞的细胞毒性作用。流式细胞术检测显示,含GFW的大鼠含药血清可使罗丹明123蓄积增加;蛋白质免疫印迹分析表明,含药血清可使SKOV3/DDP细胞中P-糖蛋白、丝氨酸473位点磷酸化的AKT及mTOR蛋白水平呈剂量依赖性降低,但对PI3K p110α和总AKT蛋白水平无影响。低剂量的GFW可增强顺铂和紫杉醇对耐药SKOV3/DDP异种移植瘤的抗癌疗效。GFW可能通过抑制P-糖蛋白的蛋白水平和功能,使顺铂耐药的SKOV3/DDP细胞致敏,其机制可能与PI3K/AKT/mTOR信号通路失活有关。