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z-古古甾酮是阿育吠陀药用植物没药树的一种成分,在体外和体内均能抑制血管生成。

z-Guggulsterone, a constituent of Ayurvedic medicinal plant Commiphora mukul, inhibits angiogenesis in vitro and in vivo.

作者信息

Xiao Dong, Singh Shivendra V

机构信息

Department of Pharmacology and University of Pittsburgh Cancer Institute, School of Medicine, Pittsburgh, PA 15213, USA.

出版信息

Mol Cancer Ther. 2008 Jan;7(1):171-80. doi: 10.1158/1535-7163.MCT-07-0491.

Abstract

Our previous studies have shown that z-guggulsterone, a constituent of Indian Ayurvedic medicinal plant Commiphora mukul, inhibits the growth of human prostate cancer cells by causing apoptosis. We now report a novel response to z-guggulsterone involving the inhibition of angiogenesis in vitro and in vivo. The z-guggulsterone treatment inhibited capillary-like tube formation (in vitro neovascularization) by human umbilical vein endothelial cells (HUVEC) and migration by HUVEC and DU145 human prostate cancer cells in a concentration- and time-dependent manner. The z- and E-isomers of guggulsterone seemed equipotent as inhibitors of HUVEC tube formation. The z-guggulsterone-mediated inhibition of angiogenesis in vitro correlated with the suppression of secretion of proangiogenic growth factors [e.g., vascular endothelial growth factor (VEGF) and granulocyte colony-stimulating factor], down-regulation of VEGF receptor 2 (VEGF-R2) protein level, and inactivation of Akt. The z-guggulsterone-mediated suppression of DU145 cell migration was increased by knockdown of VEGF-R2 protein level. Ectopic expression of constitutively active Akt in DU145 cells conferred protection against z-guggulsterone-mediated inhibition of cell migration. Oral gavage of 1 mg z-guggulsterone/d (five times/wk) to male nude mice inhibited in vivo angiogenesis in DU145-Matrigel plug assay as evidenced by a statistically significant decrease in tumor burden, microvessel area (staining for angiogenic markers factor VIII and CD31), and VEGF-R2 protein expression. In conclusion, the present study reveals that z-guggulsterone inhibits angiogenesis by suppressing the VEGF-VEGF-R2-Akt signaling axis. Together, our results provide compelling rationale for further preclinical and clinical investigation of z-guggulsterone for its efficacy against prostate cancer.

摘要

我们之前的研究表明,印度阿育吠陀药用植物没药(Commiphora mukul)的成分Z-古古甾酮可通过诱导细胞凋亡来抑制人前列腺癌细胞的生长。我们现在报告Z-古古甾酮的一种新作用,即其在体外和体内均可抑制血管生成。Z-古古甾酮处理以浓度和时间依赖性方式抑制人脐静脉内皮细胞(HUVEC)形成毛细血管样管(体外新血管形成)以及HUVEC和DU145人前列腺癌细胞的迁移。古古甾酮的Z-异构体和E-异构体作为HUVEC管形成抑制剂似乎具有同等效力。Z-古古甾酮在体外介导的血管生成抑制与促血管生成生长因子[如血管内皮生长因子(VEGF)和粒细胞集落刺激因子]分泌的抑制、VEGF受体2(VEGF-R2)蛋白水平的下调以及Akt的失活相关。通过敲低VEGF-R2蛋白水平可增强Z-古古甾酮介导的对DU145细胞迁移的抑制作用。在DU145细胞中组成型激活的Akt的异位表达可赋予细胞对Z-古古甾酮介导的细胞迁移抑制的抗性。在雄性裸鼠中每日经口灌胃1 mg Z-古古甾酮(每周5次)在DU145-基质胶栓试验中抑制体内血管生成,这表现为肿瘤负荷、微血管面积(血管生成标志物因子VIII和CD31染色)和VEGF-R2蛋白表达的统计学显著降低。总之,本研究揭示Z-古古甾酮通过抑制VEGF-VEGF-R2-Akt信号轴来抑制血管生成。总之,我们的结果为进一步对Z-古古甾酮抗前列腺癌疗效进行临床前和临床研究提供了令人信服的理论依据。

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