Quercetin inhibits the expression and function of the androgen receptor in LNCaP prostate cancer cells

被引:206
作者
Xing, NZ [1 ]
Chen, Y [1 ]
Mitchell, SH [1 ]
Young, CYF [1 ]
机构
[1] Mayo Fdn, Mayo Grad Sch, Dept Urol & Biochem & Mol Biol, Rochester, MN 55905 USA
关键词
D O I
10.1093/carcin/22.3.409
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The androgen receptor (AR) is involved in the development and progression of prostate cancer. In order to find new compounds that may present novel mechanisms to attenuate the function of AR, we investigated the effect of a natural flavonoid chemical, quercetin, on androgen action in an androgen-responsive LNCaP prostate cancer cell line. Western blot analysis showed that AR protein expression was inhibited by quercetin in a dose-dependent manner. To demonstrate that the repression effects on AR expression can actually reduce its function, we found that quercetin inhibited the secretion of the prostate-specific, androgen-regulated tumor markers, PSA and hK2, The mRNA levels of androgen-regulated genes such as PSA, NKX3.1 as well as ornithine decarboxylase (ODC) were down-regulated by quercetin. Transient transfections further showed that quercetin inhibited AR-mediated PSA expression at the transcription level. Finally, it was demonstrated that quercetin could repress the expression of the AR gene at the transcription level. Our result suggests that quercetin can attenuate the function of AR by repressing its expression and has the potential to become a chemopreventive and/or chemotherapeutic agent for prostate cancer.
引用
收藏
页码:409 / 414
页数:6
相关论文
共 50 条
[1]   A RAPID MICROPREPARATION TECHNIQUE FOR EXTRACTION OF DNA-BINDING PROTEINS FROM LIMITING NUMBERS OF MAMMALIAN-CELLS [J].
ANDREWS, NC ;
FALLER, DV .
NUCLEIC ACIDS RESEARCH, 1991, 19 (09) :2499-2499
[2]  
ANDREWS PE, 1992, CANCER RES, V52, P1525
[3]   ORNITHINE DECARBOXYLASE ACTIVITY IS CRITICAL FOR CELL-TRANSFORMATION [J].
AUVINEN, M ;
PAASINEN, A ;
ANDERSSON, LC ;
HOLTTA, E .
NATURE, 1992, 360 (6402) :355-358
[4]   Androgen regulation of ornithine decarboxylase in human prostatic cells identified using differential display [J].
Betts, AM ;
Waite, I ;
Neal, DE ;
Robson, CN .
FEBS LETTERS, 1997, 405 (03) :328-332
[5]   Roles for Nkx3.1 in prostate development and cancer [J].
Bhatia-Gaur, R ;
Donjacour, AA ;
Sciavolino, PJ ;
Kim, M ;
Desai, N ;
Young, P ;
Norton, CR ;
Gridley, T ;
Cardiff, RD ;
Cunha, GR ;
Abate-Shen, C ;
Shen, MM .
GENES & DEVELOPMENT, 1999, 13 (08) :966-977
[6]   STRUCTURAL-ANALYSIS OF COMPLEMENTARY-DNA AND AMINO-ACID SEQUENCES OF HUMAN AND RAT ANDROGEN RECEPTORS [J].
CHANG, CS ;
KOKONTIS, J ;
LIAO, SS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (19) :7211-7215
[7]  
Charlesworth MC, 1999, J ANDROL, V20, P220
[8]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[9]   Molecular mechanisms in the antiproliferative action of quercetin [J].
Csokay, B ;
Prajda, N ;
Weber, G ;
Olah, E .
LIFE SCIENCES, 1997, 60 (24) :2157-2163
[10]  
Culig Z, 1998, PROSTATE, V35, P63, DOI 10.1002/(SICI)1097-0045(19980401)35:1<63::AID-PROS9>3.0.CO