首页> 外文期刊>World journal of gastroenterology : >Anti-cancer and anti-angiogenic effects of curcumin and tetrahydrocurcumin on implanted hepatocellular carcinoma in nude mice.
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Anti-cancer and anti-angiogenic effects of curcumin and tetrahydrocurcumin on implanted hepatocellular carcinoma in nude mice.

机译:姜黄素和四氢姜黄素对裸鼠移植性肝细胞癌的抗癌和抗血管生成作用。

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AIM: To determine the effect of tetrahydrocurcumin (THC) on tumor angiogenesis compared with curcumin (CUR) by using both in vitro and in vivo models of human hepatocellular carcinoma cell line (HepG2). METHODS: The 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-tetrazolium bromide (MTT) assay was used for testing the anti-proliferating activities of CUR and THC. In male BALB/c nude mice, 2 multiply 10(6) human HepG2 cells were inoculated onto a dorsal skin-fold chamber. One day after HepG2 inoculation, the experimental groups were fed oral daily with CUR or THC (300 mg/kg or 3000 mg/kg). On d 7, 14 and 21, the tumor microvasculature was observed using fluorescence videomicroscopy and capillary vascularity (CV) was measured. RESULTS: Pathological angiogenic features including microvascular dilatation, tortuosity, and hyper-permeability were observed. CUR and THC could attenuate these pathologic features. In HepG2-groups, the CV were significantly increased on d 7 (52.43%), 14 (69.17%), and 21 (74.08%), as compared to controls (33.04%, P < 0.001). Treatment with CUR and THC resulted in significant decrease in the CV (P < 0.005 and P < 0.001, respectively). In particular, the anti-angiogenic effects of CUR and THC were dose-dependent manner. However, the beneficial effect of THC treatment than CUR was observed, in particular, from the 21 d CV (44.96% and 52.86%, P < 0.05). CONCLUSION: THC expressed its anti-angiogenesis without any cytotoxic activities to HepG2 cells even at the highest doses. It is suggested that anti-angiogenic properties of CUR and THC represent a common potential mechanism for their anti-cancer actions.
机译:目的:通过使用人肝癌细胞系(HepG2)的体内和体外模型,确定与姜黄素(CUR)相比,四氢姜黄素(THC)对肿瘤血管生成的作用。方法:采用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四唑(MTT)法检测CUR和THC的抗增殖活性。在雄性BALB / c裸鼠中,将2批10(6)个人的HepG2细胞接种到背部皮肤折叠室中。接种HepG2后一天,每天给实验组口服CUR或THC(300 mg / kg或3000 mg / kg)。在第7、14和21天,使用荧光视频显微镜观察肿瘤微血管,并测量毛细血管(CV)。结果:观察到病理性血管生成特征,包括微血管扩张,曲折和高通透性。 CUR和THC可以减弱这些病理特征。在HepG2组中,与对照组(33.04%,P <0.001)相比,第7天(52.43%),14(69.17%)和21(74.08%)的CV显着增加。用CUR和THC治疗导致CV显着降低(分别为P <0.005和P <0.001)。特别地,CUR和THC的抗血管生成作用是剂量依赖性的。然而,特别是从21 d CV观察到THC治疗比CUR有益(44.96%和52.86%,P <0.05)。结论:THC即使在最高剂量下也能表达抗血管生成作用,对HepG2细胞无任何细胞毒活性。提示CUR和THC的抗血管生成特性代表了其抗癌作用的共同潜在机制。

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