School of Chinese Traditional Medicine, School of Pharmaceutical Sciences, Southwest University, Chongqing 400716, China.
Department of Clinical Laboratory, Hunan University of Medicine, Hunan 418000, China.
Sci Rep. 2017 Feb 6;7:38524. doi: 10.1038/srep38524.
Colorectal cancer is one of the most common causes of cancer-related death in humans. Coptisine (COP) is a natural alkaloid from Coptidis Rhizoma with unclear antitumor mechanism. Human colon cancer cells (HCT-116) and xenograft mice were used to systematically explore the anti-tumor activity of COP in this study. The results indicated that COP exhibited remarkably cytotoxic activities against the HCT-116 cells by inducing G-phase cell cycle arrest and increasing apoptosis, and preferentially inhibited the survival pathway and induced the activation of caspase proteases family of HCT-116 cells. Experimental results on male BALB/c nude mice confirmed that orally administration of COP at high-dose (150 mg/kg) could suppress tumor growth, and may reduce cancer metastasis risk by inhibiting the RAS-ERK pathway in vivo. Taken together, the results suggested that COP may be potential as a novel anti-tumor candidate in the HCT-116 cells-related colon cancer, further studies are still needed to suggest COP for the further use.
结直肠癌是人类癌症相关死亡的最常见原因之一。黄连碱(COP)是黄连根茎中的一种天然生物碱,其抗肿瘤机制尚不清楚。本研究用人结肠癌细胞(HCT-116)和异种移植小鼠系统地研究了 COP 的抗肿瘤活性。结果表明,COP 通过诱导 G 期细胞周期停滞和增加细胞凋亡,对 HCT-116 细胞表现出显著的细胞毒性作用,并且优先抑制存活途径并诱导 caspase 蛋白酶家族在 HCT-116 细胞中的激活。在雄性 BALB/c 裸鼠上的实验结果证实,高剂量(150mg/kg)口服 COP 能够抑制肿瘤生长,并可能通过抑制体内 RAS-ERK 通路降低癌症转移风险。总之,这些结果表明,COP 可能是一种新型的抗 HCT-116 细胞相关结肠癌的候选药物,仍需要进一步的研究来建议 COP 的进一步应用。