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黄连小檗碱抑制体外和体内 HCT-116 细胞相关肿瘤生长。

Coptisine from Rhizoma Coptidis Suppresses HCT-116 Cells-related Tumor Growth in vitro and in vivo.

机构信息

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.

出版信息

Sci Rep. 2017 Feb 6;7:38524. doi: 10.1038/srep38524.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81c6/5292956/4f4d64267822/srep38524-f1.jpg

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