Androgens, lipogenesis and prostate cancer

被引:138
作者
Swinnen, JV [1 ]
Heemers, H [1 ]
de Sande, TV [1 ]
De Schrijver, E [1 ]
Brusselmans, K [1 ]
Heyns, W [1 ]
Verhoeven, G [1 ]
机构
[1] Univ Leuven, Lab Expt Med & Endocrinol, B-3000 Louvain, Belgium
关键词
androgens; lipogenesis; prostate cancer; SREBP; fatty acid synthase;
D O I
10.1016/j.jsbmb.2004.10.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Both experimental and epidemiological data indicate that androgens are among the main factors controlling the development, maintenance and progression of prostate cancer. Identifying the genes that are regulated by androgens represents a major step towards the elucidation of the mechanisms underlying the impact of androgens on prostate cancer cell biology and is an attractive approach to find novel targets for prostate cancer therapy. Among the genes that have been identified thus far, several genes encode lipogenic enzymes. Studies aimed at the elucidation of the mechanisms underlying androgen regulation of lipogenic genes revealed that androgens coordinately stimulate the expression of these genes through interference with the molecular mechanism controlling activation of sterol regulatory element-binding proteins (SREBPs), lipogenic transcription factors governing cellular lipid homeostasis. The resulting increase in lipogenesis serves the synthesis of key membrane components (phospholipids, cholesterol) and is a major hallmark of cancer cells. Pharmacologic inhibition of lipogenesis or RNA-interference-mediated down-regulation of key lipogenic genes induces apoptosis in cancer cell lines and reduces tumor growth in xenograft models. While increased lipogenesis is already found in the earliest stages of cancer development (PIN) and initially is androgen-responsive it persists or re-emerges with the development of androgen-independent cancer, indicating that lipogenesis is a fundamental aspect of prostate cancer cell biology and is a potential target for chernoprevention and for antineoplastic therapy in advanced prostate cancer. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:273 / 279
页数:7
相关论文
共 58 条
  • [1] AHLUWALIA B, 1981, CANCER, V48, P2267, DOI 10.1002/1097-0142(19811115)48:10<2267::AID-CNCR2820481023>3.0.CO
  • [2] 2-R
  • [3] Cell surface polarization during yeast mating
    Bagnat, M
    Simons, K
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (22) : 14183 - 14188
  • [4] Bosland M C, 2000, J Natl Cancer Inst Monogr, P39
  • [5] Regulated intramembrane proteolysis: A control mechanism conserved from bacteria to humans
    Brown, MS
    Ye, J
    Rawson, RB
    Goldstein, JL
    [J]. CELL, 2000, 100 (04) : 391 - 398
  • [6] Epigallocatechin-3-gallate is a potent natural inhibitor of fatty acid synthase in intact cells and selectively induces apoptosis in prostate cancer cells
    Brusselmans, K
    De Schrijver, E
    Heyns, W
    Verhoeven, G
    Swinnen, JV
    [J]. INTERNATIONAL JOURNAL OF CANCER, 2003, 106 (06) : 856 - 862
  • [7] BRWAER MK, 1995, J UROLOGY, V153, P115
  • [8] PROGESTINS AND ANDROGENS STIMULATE LIPID-ACCUMULATION IN T47D BREAST-CANCER CELLS VIA THEIR OWN RECEPTORS
    CHAMBON, M
    ROCHEFORT, H
    VIAL, HJ
    CHALBOS, D
    [J]. JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1989, 33 (05) : 915 - 922
  • [9] Androgen receptors in prostate cancer
    Culig, ZR
    Klocker, H
    Bartsch, G
    Steiner, H
    Hobisch, A
    [J]. JOURNAL OF UROLOGY, 2003, 170 (04) : 1363 - 1369
  • [10] INHIBITION OF FATTY-ACID SYNTHESIS BY ANTIBIOTIC CERULENIN - SPECIFIC INACTIVATION OF BETA-KETOACYL-ACYL CARRIER PROTEIN SYNTHETASE
    DAGNOLO, G
    ROSENFELD, IS
    AWAYA, J
    OMURA, S
    VAGELOS, PR
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1973, 326 (02) : 155 - 166