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首页> 外文期刊>Phytotherapy research: PTR >Inhibitory Effects of the Aqueous Extract of Magnolia officinalis on the Responses of Human Urinary Bladder Cancer 5637 Cells In Vitro and Mouse Urinary Bladder Tumors induced by N-Butyl-N-(4-hydroxybutyl) nitrosamine In Vivo
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Inhibitory Effects of the Aqueous Extract of Magnolia officinalis on the Responses of Human Urinary Bladder Cancer 5637 Cells In Vitro and Mouse Urinary Bladder Tumors induced by N-Butyl-N-(4-hydroxybutyl) nitrosamine In Vivo

机译:厚朴水提取物对N-丁基-N-(4-羟丁基)亚硝胺体内诱导的人膀胱癌5637细胞体外和小鼠膀胱膀胱肿瘤反应的抑制作用

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摘要

This study investigated the anticancer activity of Magnolia officinalis on urinary bladder cancer in vitro and in vivo, and elucidated the mechanism of its activity. An aqueous extract of M. officinalis inhibited cell viability and DNA synthesis in cultured human urinary bladder cancer 5637 cells. Inhibition of proliferation was the result of apoptotic induction, because FACS analyses of 5637 cells treated with M. officinalis showed a sub-G1 phase accumulation. M. officinalis extract also increased cytoplasmic DNA-histone complex dose-dependently. These inhibitory effects were associated with the upregulation of proapoptotic molecules Bax, cytochrome c and caspase 3. Treatment of 5637 cells with M. officinalis extract suppressed the expression of matrix metalloproteinase 2 (MMP-2) and MMP-9, as revealed by zymographic and immunoblot analyses. When M. officinalis extract was given to mice simultaneously with the carcinogen N-butyl-N-(4-hvdroxybutyl) nitrosamine, which induces urinary bladder tumors, the size of the induced tumors was smaller. Finally, histological data indicated that the histological grade of carcinoma and the depth of invasion were dramatically decreased by treatment with M. officinalis extract in mice with N-butyl-N-(4-hydroxybutyl) nitrosamine-induced urinary bladder tumors. In conclusion, the findings showed that M. officinalis extract exhibited potential chemopreventive activity against urinary bladder tumor in vitro and in vivo. Copyright (c) 2008 John Wiley & Sons, Ltd.
机译:这项研究调查了木兰对膀胱癌的体内外抗癌活性,并阐明了其活性机制。山茱M的水提取物抑制了培养的人膀胱癌5637细胞的细胞活力和DNA合成。增殖抑制是细胞凋亡诱导的结果,因为通过流式细胞仪分析了用厚朴分枝杆菌处理的5637细胞,发现亚G1期积累。山茱。提取物也可剂量依赖性地增加细胞质DNA-组蛋白复合物。这些抑制作用与细胞凋亡分子Bax,细胞色素c和caspase 3的上调相关。如酶谱法和酶切法所揭示的那样,用厚朴分枝杆菌提取物处理5637细胞可抑制基质金属蛋白酶2(MMP-2)和MMP-9的表达。免疫印迹分析。当将药用厚朴提取物与致癌物N-丁基-N-(4-羟基丁氧基)亚硝胺同时给予小鼠时,诱导的肿瘤的尺寸较小。最后,组织学数据表明,在N-丁基-N-(4-羟丁基)亚硝胺诱导的膀胱肿瘤小鼠中,用厚朴提取物治疗可显着降低癌的组织学等级和浸润深度。总之,研究结果表明,山茱M提取物在体外和体内对膀胱肿瘤均具有潜在的化学预防活性。版权所有(c)2008 John Wiley&Sons,Ltd.

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