Mon May Thuu, Yodkeeree Supachai, Punfa Wanisa, Pompimon Wilart, Limtrakul Pornngarm
Department of Biochemistry, Faculty of Medicine, Chiang Mai University.
Department of Biochemistry, University of Medicine-2.
Chem Pharm Bull (Tokyo). 2018;66(2):162-169. doi: 10.1248/cpb.c17-00687.
Crebanine (CN), tetrahydropalmatine (THP), O-methylbulbocapnine (OMBC) and N-methyl tetrahydropalmatine (NMTHP) are isoquinoline derived natural alkaloids isolated from tubers of Stephania venosa. We investigated chemo-sensitizing effects of these alkaloids in ovarian cancer cells and evaluated underlying molecular mechanisms involved in chemo-sensitivity. Detection of cell apoptosis was evaluated by using flow cytometry. Cell viability was analyzed using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. Chou-Talalay median effect principle was used to evaluate potential drug interactions. Protein analyses were performed on ovarian carcinoma cells using Western blotting upon treatment with anticancer drug and alkaloids. Aporphine alkaloids, such as CN and OMBC, enhanced cisplatin sensitivity in intrinsic cisplatin resistant SKOV3 cells, but not in cisplatin sensitive A2780 cells. Protoberberine alkaloids, such as THP and NMTHP, had no synergistic effect on cisplatin sensitivity in either cell line. Chemo-sensitizing effects of CN and OMBC in SKOV3 cells were mediated via activating apoptosis-induced cell death through caspase-3, -8 and cleaved poly ADP-ribose polymerase (PARP) and via inhibiting anti-apopotic and survival protein expression, such as Bcl-xL, Baculoviral IAP repeat-containing protein 3 (cIAP-2), survivin and interleukin (IL) -6. Cisplatin stimulated protein kinase B (Akt) and nuclear factor-kappaB (NF-κB) signaling pathways, but not mitogen-activated protein kinase (MAPK), activator protein 1 (AP-1) and signal transducer and activator of transcription 3 (STAT3) in SKOV3 cells. Akt/NF-κB signaling was blocked by CN and OMBC leading to increased sensitization to cisplatin. These findings demonstrate that CN and OMBC sensitizes SKOV3 cells to cisplatin via inhibition of Akt/NF-κB signaling and the down regulation of NF-κB mediated gene products. Our results suggest that alkaloids obtained from S. venosa could be used as chemo-sensitizers in ovarian cancer to sensitize and minimize the dose related toxicity of platinum-based chemotherapeutic drugs.
克班宁(CN)、四氢巴马汀(THP)、O - 甲基去甲乌药碱(OMBC)和N - 甲基四氢巴马汀(NMTHP)是从地不容块茎中分离得到的异喹啉衍生天然生物碱。我们研究了这些生物碱对卵巢癌细胞的化学增敏作用,并评估了涉及化学敏感性的潜在分子机制。使用流式细胞术评估细胞凋亡检测。使用3 -(4,5 - 二甲基噻唑 - 2 - 基)- 2,5 - 二苯基四氮唑溴盐(MTT)法分析细胞活力。采用Chou - Talalay中位效应原理评估潜在的药物相互作用。在用抗癌药物和生物碱处理后,使用蛋白质印迹法对卵巢癌细胞进行蛋白质分析。阿朴啡生物碱,如CN和OMBC,增强了内在顺铂耐药的SKOV3细胞对顺铂的敏感性,但对顺铂敏感的A2780细胞没有作用。原小檗碱生物碱,如THP和NMTHP,对这两种细胞系的顺铂敏感性均无协同作用。CN和OMBC在SKOV3细胞中的化学增敏作用是通过激活由半胱天冬酶 - 3、 - 8和裂解的聚ADP - 核糖聚合酶(PARP)诱导的细胞凋亡以及抑制抗凋亡和存活蛋白表达,如Bcl - xL、含杆状病毒IAP重复序列蛋白3(cIAP - 2)、存活素和白细胞介素(IL) - 6来介导的。顺铂刺激SKOV3细胞中的蛋白激酶B(Akt)和核因子 - κB(NF - κB)信号通路,但不刺激丝裂原活化蛋白激酶(MAPK)、活化蛋白1(AP - 1)和信号转导及转录激活因子3(STAT3)。CN和OMBC阻断了Akt/NF - κB信号通路,导致对顺铂的敏感性增加