首页> 外文期刊>Plant Foods for Human Nutrition >Soy-derived isoflavones inhibit HeLa cell growth by inducing apoptosis.
【24h】

Soy-derived isoflavones inhibit HeLa cell growth by inducing apoptosis.

机译:大豆异黄酮通过诱导细胞凋亡来抑制HeLa细胞的生长。

获取原文
获取原文并翻译 | 示例
           

摘要

Isoflavones are among the major bioactive compounds found in a wide variety of plant-derived foods, especially in soybeans and soy-based foods. In this study, the effect of a soy-derived isoflavone mixture (designated as SI-I, containing 71% daidzein, 14.3% genistein and 14.7% glycitein) on HeLa cells and its mechanism were investigated. SI-I in concentration range 5-80 mug/ml significantly reduced the survival rate of HeLa cells by MTT assay, whereas showed no side effect on that of L929 cells. After HeLa cells were exposed to 10, 20 and 40 mug/ml SI-I for 4 days, typical apoptotic morphological changes, including nuclear fragmentation, cytoplasm shrinkage and decrease of cell volume, were observed by fluorescence microscope and CLSM, respectively. FCM analysis revealed that the percentages of early apoptotic cells with lost Delta psim increased by 2.27, 2.74 and 4.05 folds respectively, compared with control. The results showed that SI-I inhibited HeLa cell growth through inducing apoptosis via the mitochondrial pathway and comparisons with reported data indicated that synergistic effect existed between the isoflavone species contained in SI-I. It is proposed that natural soy-derived isoflavones are potential candidates as chemoterapeutic agents against human cervical cancer. copyright Springer Science+Business Media, LLC 2011.
机译:异黄酮是在多种植物来源的食品中发现的主要生物活性化合物之一,尤其是在大豆和大豆类食品中。在这项研究中,研究了大豆异黄酮混合物(命名为SI-1,包含71%的大豆苷元,14.3%的染料木黄酮和14.7%的糖精)对HeLa细胞的作用及其机制。通过MTT分析,浓度范围为5-80杯子/毫升的SI-1显着降低了HeLa细胞的存活率,而对L929细胞没有副作用。将HeLa细胞分别暴露于10、20和40 mug / ml SI-I 4天后,分别通过荧光显微镜和CLSM观察到典型的凋亡形态变化,包括核碎裂,细胞质收缩和细胞体积减少。 FCM分析显示,与对照组相比,缺失Δpsim的早期凋亡细胞百分比分别增加了2.27、2.74和4.05倍。结果表明,SI-1通过线粒体途径诱导细胞凋亡来抑制HeLa细胞的生长,并与报道的数据进行比较表明SI-1中所含异黄酮之间存在协同作用。有人提出,天然大豆衍生的异黄酮可能作为抗人宫颈癌的化学治疗剂。版权所有Springer Science + Business Media,LLC 2011。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号