Ginsenoside 20(S)-protopanaxadiol inhibits the proliferation and invasion of human fibrosarcoma HT1080 cells

被引:54
作者
Li, Gang
Wang, Zhenhua
Sun, Yaxuan
Liu, Ke
Wang, Ziren [1 ]
机构
[1] Lanzhou Univ, Sch Life Sci, Lanzhou 730000, Peoples R China
[2] Yantai Univ, Sch Pharm, Yantai, Peoples R China
[3] Res Inst Luye Pharm, Yantai, Peoples R China
关键词
D O I
10.1111/j.1742-7843.2006.pto_415.x
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
Ginsenoside 20(S)-protopanaxadiol, one of metabolites of ginseng saponins, has been well characterized to possess the pleiotropic anticancer capabilities in several cancer cell lines. The object of this study was to investigate the effects of ginsenoside 20(S)-protopanaxadiol on the invasion in vitro and the expression of matrix metalloprotemase-2 in human fibrosarcoma HT1080 cells in absence of cytotoxicity. Our results showed that ginsenoside 20(S)-protopanaxadiol exerted a concentration-dependent inhibitory effect on the proliferation of HT1080 Cells (IC50 was 76.78 +/- 2.24 mu M, 48 hr). Treatment with 20(S)-protopanaxadiol significantly declined the invasive capacity of HT1080 cells compared to the control cells (P < 0.01) in the in vitro invasion assay. Further analysis with gelatin zymography and western blotting revealed that both the activity and the expression of matrix metalloprotemase-2 decreased dramatically in a concentration-dependent manner (P < 0.01). Taken together, these results indicated that ginsenoside 20(S)-protopanaxadiol is able to inhibit the invasiveness of HT1080 cells significantly in vitro and this action may be primarily due to down-regulating the expression of matrix metalloproteinase-2. Ginsenoside 20(S)-protopanaxadiol, a metabolite of ginseng, may be applied as a potential therapeutic agent in the prevention and treatment of cancer.
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收藏
页码:588 / 592
页数:5
相关论文
共 28 条
[1]
Ginseng pharmacology - Multiple constituents and multiple actions [J].
Attele, AS ;
Wu, JA ;
Yuan, CS .
BIOCHEMICAL PHARMACOLOGY, 1999, 58 (11) :1685-1693
[2]
Chang Yuan S, 2003, Integr Cancer Ther, V2, P13, DOI 10.1177/1534735403251167
[3]
Invasive growth: from development to metastasis [J].
Comoglio, PM ;
Trusolino, L .
JOURNAL OF CLINICAL INVESTIGATION, 2002, 109 (07) :857-862
[4]
Fishman DA, 2001, CANCER RES, V61, P3194
[5]
Ginsenosides inhibit EGF-induced proliferation of renal proximal tubule cells via decrease of c-fos and c-jun gene expression in vitro [J].
Han, HJ ;
Yoon, BC ;
Lee, SH ;
Park, SH ;
Park, JY ;
Oh, YJ ;
Lee, YJ .
PLANTA MEDICA, 2002, 68 (11) :971-974
[6]
Main Ginseng saponin metabolites formed by intestinal bacteria [J].
Hasegawa, H ;
Sung, JH ;
Matsumiya, S ;
Uchiyama, M .
PLANTA MEDICA, 1996, 62 (05) :453-457
[7]
HUHTALA P, 1991, J BIOL CHEM, V266, P16485
[8]
Preventive effect of epicatechin and ginsenoside Rb2 on the inhibition of gap junctional intercellular communication by TPA and H2O2 [J].
Kang, KS ;
Kang, BC ;
Lee, BJ ;
Che, JH ;
Li, GX ;
Trosko, JE ;
Lee, YS .
CANCER LETTERS, 2000, 152 (01) :97-106
[9]
KARIKURA M, 1991, CHEM PHARM BULL, V39, P2357
[10]
The possible role of matrix metalloproteinase (MMP)-2 and MMP-9 in cancer, e.g. acute leukemia [J].
Klein, G ;
Vellenga, E ;
Fraaije, MW ;
Kamps, WA ;
de Bont, ESJM .
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2004, 50 (02) :87-100