Li Chuan, Wang Yihai, Wang Chunhua, Yi Xiaomin, Li Mingya, He Xiangjiu
School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou 510006, China; Guangdong Engineering Research Center for Lead Compounds & Drug Discovery, Guangzhou 510006, China.
School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou 510006, China.
Phytomedicine. 2017 May 15;28:10-18. doi: 10.1016/j.phymed.2017.02.008. Epub 2017 Feb 28.
Harmine, a β-carboline alkaloid from Peganum harmala, has multiple anti-tumor activities, especially for its folk therapy for digestive system neoplasm. However, the underlying mechanism of harmine on gastric cancer remains unclear.
To illuminate the potential anti-tumor activity and mechanism of harmine against gastric cancer cells.
METHODS/STUDY DESIGNS: The anti-proliferative activity of harmine in vitro was evaluated by MTT assay. The autophagic activity induced by harmine was assessed using GFP-LC3 transfection. FITC/PI double staining was applied for the apoptosis inspection. The mitochondrial membrane potential was detected by JC-1 fluorescence probe. The potential mechanisms for proteins level in autophagy and apoptosis were analyzed by Western blot.
Harmine exhibited potent effects on both autophagy and apoptosis. Treatment with harmine could enhance dots of GFP-LC3 in cells. Meanwhile, the process had connection with Beclin-1, LC3-II, and p62 by the inhibition of Akt/mTOR/p70S6K signaling. However, high concentration of harmine led to apoptosis characterized by the propidium/Annexin V-positive cell pollution, cell shrunk and the collapse of mitochondrial membrane potential. The regulation of Bcl-2, Bax and the gathering of cleaved-PARP, cleaved-caspase 3 and cleaved-caspase 9 contributed to the induction of apoptosis. In addition, 10μM LY294002 (a specific inhibitor of PI3K/Akt) combination with 40μM harmine significantly increased the cytotoxicity to the gastric cancer cells and up-regulated both the apoptosis-related protein (cleaved-PARP, cleaved-caspase-3) and autophagy-related protein (Beclin-1, LC3-II, and p62). Adding the inhibitor of autophagy, 3-MA or BafA1, increased the viability of harmine-exposured gastric cancer cells, which confirmed the role of autophagy played in the gastric cancer cell death induced by harmine.
Harmine might be a potent inducer of apoptosis and autophagy, which offered evidences to therapy of harmine in gastric carcinoma in the folk medicine.
骆驼蓬碱是一种从骆驼蓬中提取的β-咔啉生物碱,具有多种抗肿瘤活性,尤其在消化系统肿瘤的民间治疗中应用广泛。然而,骆驼蓬碱对胃癌的潜在作用机制仍不清楚。
阐明骆驼蓬碱对胃癌细胞的潜在抗肿瘤活性及其作用机制。
方法/研究设计:采用MTT法评估骆驼蓬碱在体外的抗增殖活性。利用绿色荧光蛋白-微管相关蛋白1轻链3(GFP-LC3)转染评估骆驼蓬碱诱导的自噬活性。采用异硫氰酸荧光素/碘化丙啶(FITC/PI)双染法检测细胞凋亡。用JC-1荧光探针检测线粒体膜电位。通过蛋白质免疫印迹法分析自噬和凋亡相关蛋白水平的潜在机制。
骆驼蓬碱对自噬和凋亡均有显著影响。用骆驼蓬碱处理可增加细胞中GFP-LC3的点状聚集。同时,该过程通过抑制Akt/哺乳动物雷帕霉素靶蛋白(mTOR)/核糖体蛋白S6激酶1(p70S6K)信号通路与自噬相关蛋白1(Beclin-1)、微管相关蛋白1轻链3-II(LC3-II)和p62相关。然而,高浓度的骆驼蓬碱会导致细胞凋亡,表现为碘化丙啶/膜联蛋白V双阳性细胞增多、细胞皱缩和线粒体膜电位丧失。B细胞淋巴瘤-2(Bcl-2)、Bax蛋白的调节以及裂解的聚(ADP-核糖)聚合酶(cleaved-PARP)、裂解的半胱天冬酶-3(cleaved-caspase 3)和裂解的半胱天冬酶-9(cleaved-caspase 9)的聚集促成了细胞凋亡的诱导。此外,10μM的LY294002(一种磷脂酰肌醇-3激酶/蛋白激酶B(PI3K/Akt)的特异性抑制剂)与40μM的骆驼蓬碱联合使用可显著增加对胃癌细胞的细胞毒性,并上调凋亡相关蛋白(cleaved-PARP、cleaved-caspase-3)和自噬相关蛋白(Beclin-1、LC3-II和p62)。添加自噬抑制剂3-甲基腺嘌呤(3-MA)或巴弗洛霉素A1(BafA1)可增加暴露于骆驼蓬碱的胃癌细胞的活力,这证实了自噬在骆驼蓬碱诱导的胃癌细胞死亡中所起的作用。
骆驼蓬碱可能是一种有效的凋亡和自噬诱导剂,为其在民间医学中治疗胃癌提供了依据。