Characterization of chemical constituents in Scutellaria baicalensis with antiandrogenic and growth-inhibitory activities toward prostate carcinoma

被引:113
作者
Bonham, M
Posakony, J
Coleman, I
Montgomery, B
Simon, J
Nelson, PS
机构
[1] Univ Washington, Fred Hutchinson Canc Res Ctr, Div Human Biol, Seattle, WA 98109 USA
[2] Univ Washington, Fred Hutchinson Canc Res Ctr, Div Clin Res, Seattle, WA 98109 USA
[3] Univ Washington, Vet Affairs Puget Sound Hlth Care Syst, Dept Med, Seattle, WA 98109 USA
关键词
D O I
10.1158/1078-0432.CCR-04-1974
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Botanical preparations are widely used by patients with prostate cancer. Scutellaria baicalensis, a botanical with a long history of medicinal use in China, was a constituent of the herbal mixture PC-SPES, a product that inhibited prostate cancer growth in both laboratory and clinical studies. Due to the difficulties encountered when evaluating the efficacy of complex natural products, we sought to identify active chemical constituents within Scutellaria and determine their mechanisms of action. Experimental Design and Results: We used high-performance liquid chromatography to fractionate S. baicalensis and identified four compounds capable of inhibiting prostate cancer cell proliferation; baicalein, wogonin, neobaicalein, and skullcapflavone. Comparisons of the cellular effects induced by the entire extract versus the four-compound combination produced comparable cell cycle changes, levels of growth inhibition, and global gene expression profiles (r(2) = 0.79). Individual compounds exhibited antiandrogenic activities with reduced expression of the androgen receptor and androgen-regulated genes. In vivo, baicalein (20 mg/kg/d p.o.) reduced the growth of prostate cancer xenografts in nude mice by 55% at 2 weeks compared with placebo and delayed the average time for tumors to achieve a volume of similar to 1,000 mm(3) from 16 to 47 days (P < 0.001). Conclusions: Most of the anticancer activities of S. baicalensis can be recapitulated with four purified constituents that function in part through inhibition of the androgen receptor signaling pathway. We conclude that clinical studies evaluating the efficacy of these agents in the context of chemoprevention or the treatment of prostate cancer are warranted.
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页码:3905 / 3914
页数:10
相关论文
共 57 条
[11]   ELEVATED 12-LIPOXYGENASE MESSENGER-RNA EXPRESSION CORRELATES WITH ADVANCED-STAGE AND POOR DIFFERENTIATION OF HUMAN PROSTATE-CANCER [J].
GAO, X ;
GRIGNON, DJ ;
CHBIHI, T ;
ZACHAREK, A ;
CHEN, YQ ;
SAKR, W ;
PORTER, AT ;
CRISSMAN, JD ;
PONTES, JE ;
POWELL, IJ ;
HONN, KV .
UROLOGY, 1995, 46 (02) :227-237
[12]   Chemotherapy for prostate cancer [J].
Gilligan, T ;
Kantoff, PW .
UROLOGY, 2002, 60 (3A) :94-100
[13]  
Giovannucci E, 2002, JNCI-J NATL CANCER I, V94, P391, DOI 10.1093/jnci/94.5.391
[14]   Molecular pathway for (-)-epigallocatechin-3-gallate-induced cell cycle arrest and apoptosis of human prostate carcinoma cells [J].
Gupta, S ;
Hussain, T ;
Mukhtar, H .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2003, 410 (01) :177-185
[15]   The role of the androgen receptor in prostate cancer [J].
Huang, H ;
Tindall, DJ .
CRITICAL REVIEWS IN EUKARYOTIC GENE EXPRESSION, 2002, 12 (03) :193-207
[16]   Anxiolytic effect of wogonin, a benzodiazepine receptor ligand isolated from Scutellaria baicalensis Georgi [J].
Hui, KM ;
Huen, MSY ;
Wang, HY ;
Zheng, H ;
Sigel, E ;
Baur, R ;
Ren, H ;
Li, ZW ;
Wong, JTF ;
Xue, H .
BIOCHEMICAL PHARMACOLOGY, 2002, 64 (09) :1415-1424
[17]   Antitumor effects of Scutellariae radix and its components baicalein, baicalin, and wogonin on bladder cancer cell lines [J].
Ikemoto, S ;
Sugimura, K ;
Yoshida, N ;
Yasumoto, R ;
Wada, S ;
Yamamoto, K ;
Kishimoto, T .
UROLOGY, 2000, 55 (06) :951-955
[18]   Cancer statistics, 2002 [J].
Jemal, A ;
Thomas, A ;
Murray, T ;
Thun, M .
CA-A CANCER JOURNAL FOR CLINICIANS, 2002, 52 (01) :23-47
[19]   Select: The next prostate cancer prevention trial [J].
Klein, EA ;
Thompson, IM ;
Lippman, SM ;
Goodman, PJ ;
Albanes, D ;
Taylor, PR ;
Coltman, C .
JOURNAL OF UROLOGY, 2001, 166 (04) :1311-1315
[20]  
Landström M, 1998, PROSTATE, V36, P151, DOI 10.1002/(SICI)1097-0045(19980801)36:3&lt