Ni Xiaofen, Chen Jiajun, Lu Fengying, Yuan Zhengzhong, Xu Xiaofeng, Hu Zhen, Jiang Lei
Department of Traditional Chinese Medicine, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325000, China.
Department of Traditional Chinese Medicine, The Second Affiliated Hospital of Wenzhou Medical University, Wenzhou 325000, China.
Recent Pat Anticancer Drug Discov. 2018;13(2):240-247. doi: 10.2174/1574892813666180329163945.
α-Solanine, the most important and active component of Solanum nigrum, was found to have anti-cancer activity on multiple cancer cells. However, its effects on colorectal cancer (CRC) and associated molecular mechanisms remain to be further elucidated.
In this study, we investigated the anti-cancer effects of α-solanine against CRC cells in vitro and in vivo.
MATERIALS & METHODS: Cell viability was measured using Cell Counting Kit-8 (CCK-8) assay; cell cycle was analyzed with a Cycletest Plus DNA Reagent Kit; cell apoptosis was detected by flow cytometer; cell migration and invasive ability was determined by Transwell assays; S100P protein expression was also analyzed by western blotting; lentiviral vectors expressing shRNA targeting the S100P gene.
We demonstrated that α-solanine inhibited CRC cell (SW480, SW620 and HT-29) growth as well as migration and invasion, induced cell cycle arrest and apoptosis in vitro, and suppressed tumor growth in vivo. Moreover, we observed that S100P expression was downregulated by α-solanine. Overexpression of S100P partially reversed the α-solanine-induced growth inhibition of CRC cells. Conversely, knockdown of S100P by lentiviral-mediated RNAi resulted in significantly promoting the α-solanine-induced growth inhibition.
These findings suggest that α-solanine is a potential agent for the treatment of CRC, and the anti-tumor effect of α-solanine in the CRC cells may be mediated at least partly by the downregulation of S100P.
α-茄碱是龙葵中最重要且具有活性的成分,已发现其对多种癌细胞具有抗癌活性。然而,其对结直肠癌(CRC)的影响及相关分子机制仍有待进一步阐明。
在本研究中,我们调查了α-茄碱在体外和体内对CRC细胞的抗癌作用。
使用细胞计数试剂盒-8(CCK-8)检测法测量细胞活力;用Cycletest Plus DNA试剂试剂盒分析细胞周期;通过流式细胞仪检测细胞凋亡;用Transwell检测法测定细胞迁移和侵袭能力;也通过蛋白质印迹法分析S100P蛋白表达;构建表达靶向S100P基因的短发夹RNA(shRNA)的慢病毒载体。
我们证明α-茄碱抑制CRC细胞(SW480、SW620和HT-29)的生长以及迁移和侵袭,在体外诱导细胞周期停滞和凋亡,并在体内抑制肿瘤生长。此外,我们观察到α-茄碱下调S100P表达。S100P的过表达部分逆转了α-茄碱诱导的CRC细胞生长抑制。相反,通过慢病毒介导的RNA干扰敲低S100P导致显著增强α-茄碱诱导的生长抑制。
这些发现表明α-茄碱是一种潜在的CRC治疗药物,α-茄碱在CRC细胞中的抗肿瘤作用可能至少部分是由S100P的下调介导的。