Androgenic suppression of ATP-binding cassette transporter A1 expression in LNCaP human prostate cancer cells

被引:77
作者
Fukuchi, J
Hiipakka, RA
Kokontis, JM
Hsu, S
Ko, AL
Fitzgerald, ML
Liao, ST
机构
[1] Univ Chicago, Ben May Inst Canc Res, Chicago, IL 60637 USA
[2] Univ Chicago, Dept Biochem & Mol Biol, Chicago, IL 60637 USA
[3] Massachusetts Gen Hosp, Lipid Metab Unit, Boston, MA 02114 USA
[4] Harvard Univ, Sch Med, Boston, MA 02115 USA
关键词
D O I
10.1158/0008-5472.CAN-04-2647
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Alteration of lipid metabolism is commonly observed in sex hormone-dependent cancer cells, yet its mechanistic involvement in cancer cell proliferation and progression is unclear. We have found that the expression of the cholesterol transporter, ATP-binding cassette transporter A1 (ABCA1), was 15- to 20-fold higher in androgen-dependent than in androgen-independent LNCaP human prostate cancer cells, indicating a possible relationship between the expression levels of ABCA1 and prostate cancer progression. On the basis of real-time quantitative PCR and Western blot analysis, expression of ABCA1 in androgen-dependent cells was inhibited by androgen. The antiandrogen Casodex blocked the effect of androgen, implicating the androgen receptor in regulation of ABCA1 expression by androgens. Using an ABCA1 promoter-reporter gene assay, androgenic suppression was observed at the transcriptional level in androgen-dependent but not in androgen-independent prostate cancer cells. ABCA1 appears to have a role in modulating cell proliferation because knockdown of ABCA1 expression by RNA interference in androgen-dependent cells increased their rate of proliferation. Therefore, a suppressive effect of androgen on ABCA1 expression may be one of the mechanisms by which androgens regulate proliferation in prostate cancer cells. Attenuated ABCA1 expression in androgen-independent cells thus may contribute, in part, to prostate cancer progression.
引用
收藏
页码:7682 / 7685
页数:4
相关论文
共 21 条
[1]
ACEVEDO HF, 1973, CANCER, V32, P196, DOI 10.1002/1097-0142(197307)32:1<196::AID-CNCR2820320130>3.0.CO
[2]
2-6
[3]
The correlation of ATP-binding cassette 1 mRNA levels with cholesterol efflux from various cell lines [J].
Bortnick, AE ;
Rothblat, GH ;
Stoudt, G ;
Hoppe, KL ;
Royer, LJ ;
McNeish, J ;
Francone, OL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (37) :28634-28640
[4]
Molecular and functional interaction of the ATP-binding cassette transporter A1 with Fas-associated death domain protein [J].
Buechler, C ;
Bared, SM ;
Aslanidis, C ;
Ritter, M ;
Drobnik, W ;
Schmitz, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (44) :41307-41310
[5]
The carboxyterminus of the ATP-binding cassette transporter A1 interacts with a β2-syntrophin/utrophin complex [J].
Buechler, C ;
Boettcher, A ;
Bared, SM ;
Probst, MCO ;
Schmitz, G .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 293 (02) :759-765
[6]
Dysregulation of sterol response element-binding proteins and downstream effectors in prostate cancer during progression to androgen independence [J].
Ettinger, SL ;
Sobel, R ;
Whitmore, TG ;
Akbari, M ;
Bradley, DR ;
Gleave, ME ;
Nelson, CC .
CANCER RESEARCH, 2004, 64 (06) :2212-2221
[7]
ATP-binding cassette transporter A1 contains an NH2-terminal signal anchor sequence that translocates the protein's first hydrophilic domain to the exoplasmic space [J].
Fitzgerald, ML ;
Mendez, AJ ;
Moore, KJ ;
Andersson, LP ;
Panjeton, HA ;
Freeman, MW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (18) :15137-15145
[8]
TATA-binding protein-associated factor 7 regulates polyamine transport activity and polyamine analog-induced apoptosis [J].
Fukuchi, J ;
Hiipakka, RA ;
Kokontis, JM ;
Nishimura, K ;
Igarashi, K ;
Liao, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (29) :29921-29929
[9]
MULTIPLE PROTEIN-BINDING SITES IN THE 5'-FLANKING REGION REGULATE C-FOS EXPRESSION [J].
GILMAN, MZ ;
WILSON, RN ;
WEINBERG, RA .
MOLECULAR AND CELLULAR BIOLOGY, 1986, 6 (12) :4305-4316
[10]
SREBPs: activators of the complete program of cholesterol and fatty acid synthesis in the liver [J].
Horton, JD ;
Goldstein, JL ;
Brown, MS .
JOURNAL OF CLINICAL INVESTIGATION, 2002, 109 (09) :1125-1131