18α-glycyrrhetinic acid targets prostate cancer cells by down-regulating inflammation-related genes

被引:95
作者
Shetty, Aditya V. [1 ]
Thirugnanam, Sivasakthivel [1 ]
Dakshinamoorthy, Gajalakshmi [1 ]
Samykutty, Abhilash [1 ]
Zheng, Guoxing [1 ]
Chen, Aoshuang [1 ]
Bosland, Maarten C. [2 ]
Kajdacsy-Balla, Andre [2 ]
Gnanasekar, Munirathinam [1 ]
机构
[1] Univ Illinois, Coll Med, Dept Biomed Sci, Rockford, IL 61107 USA
[2] Univ Illinois, Dept Pathol, Chicago, IL 60612 USA
关键词
18 alpha-glycyrrhetinic acid; DU145; inflammation; invasion and prostate cancer; GLYCYRRHIZIN INDUCES APOPTOSIS; MOBILITY GROUP BOX-1; VIRUS EARLY ANTIGEN; GLYCYRRHETINIC ACID; 12-O-TETRADECANOYLPHORBOL-13-ACETATE-INDUCED INDUCTION; TUMOR ANGIOGENESIS; LICORICE EXTRACT; SERUM-LEVELS; INTERLEUKIN-8; INHIBITION;
D O I
10.3892/ijo.2011.1061
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Glycyrrhetinic acid is an active triterpenoid metabolite of glycyrrhizin abundantly present in licorice roots. Glycyrrhetinic acid exists as a and p stereo-isomeric forms. Both stereo-isomeric forms are known to have anti-inflammatory and anticancer activity. However, the effects and anticancer mechanism of a glycyrrhetinic acid in prostate cancer cells has not yet been evaluated. Therefore, we investigated the growth inhibition, induction of apoptosis and the anticancer mechanisms of 18 alpha-glycyrrhetinic acid (AGA), on the androgen-independent metastatic prostate cancer cell line DU-145. Our results showed that AGA inhibited proliferation and growth of these cells by inducing apoptosis as determined by Annexin V and flow cytometry analyses. Our studies also showed that HUVEC tube formation was drastically reduced when cultured in conditioned medium of AGA-treated DU-145 cells. In addition, AGA treatment prevented the invasion of DU-145 prostate cancer cells on matrigel coated transwells via down-regulation of NF-kappa B (p65), VEGF and MMP-9 expression. Furthermore, AGA treatment also downregulated the expression of pro-inflammatory cytokine/growth factor genes HMGB1, IL-6 and IL-8 in DU-145 cells. Interestingly, AGA simultaneously upregulated the expression of non-steroidal anti-inflammatory gene-1 (NAG-1) in DU-145 cells suggesting its anti-inflammatory activity on prostate cancer cells. Taken together, the results of this study suggest that AGA may be a promising anticancer agent that merits further investigation for the chemoprevention and treatment of prostate cancer.
引用
收藏
页码:635 / 640
页数:6
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