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首页> 外文期刊>Scientific reports. >Extracellular cholesterol oxidase production by Streptomyces aegyptia , in vitro anticancer activities against rhabdomyosarcoma, breast cancer cell-lines and in vivo apoptosis
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Extracellular cholesterol oxidase production by Streptomyces aegyptia , in vitro anticancer activities against rhabdomyosarcoma, breast cancer cell-lines and in vivo apoptosis

机译:细胞外胆固醇氧化酶生产通过链霉菌,对横纹肌肉瘤,乳腺癌细胞系和体内凋亡的体外抗癌活动产生

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In recent years, microbial cholesterol oxidases have gained great attention due to its widespread use in medical applications for serum cholesterol determination. Streptomyces aegyptia strain NEAE-102 exhibited high level of extracellular cholesterol oxidase production using a minimum medium containing cholesterol as the sole source of carbon. Fifteen variables were screened using Plackett–Burman design for the enhanced cholesterol oxidase production. The most significant variables affecting enzyme production were further optimized by using the face-centered central composite design. The statistical optimization resulted in an overall 4.97-fold increase (15.631?UmL?1) in cholesterol oxidase production in the optimized medium as compared with the unoptimized medium before applying Plackett Burman design (3.1?UmL?1). The purified cholesterol oxidase was evaluated for its in vitro anticancer activities?against five human cancer cell lines. The selectivity index values on rhabdomyosarcoma and breast cancer cell lines were 3.26 and 2.56; respectively. The in vivo anticancer activity of cholesterol oxidase was evaluated against Ehrlich solid tumor model. Compared with control mice, tumors growth was significantly inhibited in the mice injected with cholesterol oxidase alone, doxorubicin alone and cholesterol oxidase/doxorubicin combination by 60.97%, 72.99% and 97.04%; respectively. These results demonstrated that cholesterol oxidase can be used as a promising natural anticancer drug.
机译:近年来,由于其对血清胆固醇测定的医疗应用广泛使用,微生物胆固醇氧化酶越来越受到极大的关注。 Streptomyces Aegyptia菌株NEAE-102使用含有胆固醇作为唯一碳源的最小培养基表现出高水平的细胞外胆固醇氧化酶产生。使用Plackett-Burman设计进行筛选十五个变量,用于增强胆固醇氧化酶生产。通过使用面向中心的中央复合设计,进一步优化了影响酶产生的最重要的变量。在应用Plackett Burman设计之前,统计优化在优化介质中,在优化介质中,在优化培养基中的胆固醇氧化酶生产中增加了497倍(15.631〜UML?1)。评估纯化的胆固醇氧化酶,用于其体外抗癌活性?对抗五种人类癌细胞系。横纹肌肉瘤和乳腺癌细胞系上的选择性指数值为3.26和2.56;分别。对胆固醇氧化酶的体内抗癌活性对EHRLICH固体瘤模型进行了评价。与对照小鼠相比,单独使用胆固醇氧化酶,单独使用胆固醇氧化酶,胆固醇氧化酶/多柔比星组合的小鼠显着抑制了肿瘤生长,组合60.97%,72.99%和97.04%;分别。这些结果表明,胆固醇氧化酶可用作有前景的天然抗癌药物。

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