15-lipoxygenase metabolites of γ-linolenic acid/eicosapentaenoic acid suppress growth and arachidonic acid metabolism in human prostatic adenocarcinoma cells:: Possible implications of dietary fatty acids

被引:44
作者
Vang, K [1 ]
Ziboh, VA [1 ]
机构
[1] Univ Calif Davis, Sch Med, Dept Dermatol, Davis, CA 95616 USA
来源
PROSTAGLANDINS LEUKOTRIENES AND ESSENTIAL FATTY ACIDS | 2005年 / 72卷 / 05期
关键词
D O I
10.1016/j.plefa.2005.02.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Although gammalinolenic acid (GLA) and eicosapentaenoic acid (EPA) have independently been reported to suppress growth of cancer cells, their relative potencies are unknown. To determine the possible attenuating efficacies of dietary GLA or EPA on prostate carcinogenesis, we hereby report the in vitro effects of GLA, EPA and their 15-lipoxygenase (15-LOX) metabolites: 15(S)-HETrE and 15(S)-HEPE, respectively, on growth and arachidonic acid (AA) metabolism in human androgen-dependent (LNCaP) and androgen-independent (PC-3) prostatic cancer cells in culture. Specifically, both cells were preincubated respectively with the above PUFAs. Growth was determined by [H-3]thymidine uptake and AA metabolism by HPLC analysis of the extracted metabolites. Our data revealed increased biosynthesis of prostaglandin E-2 (PGE(2)) and 5-hydroxyeicosatetraenoic acid (5(S)-HETE) by both cells. Preincubation of the cells with 15(S)-HETrE or 15(S)-HEPE more markedly inhibited cellular growth and AA metabolism when compared to precursor PUFAs. Notably, 15(S)-HETrE exerted the greatest inhibitory effects. These findings therefore imply that dietary GLA rather than EPA should better attenuate prostate carcinogenesis via its in vivo generation of 15(S)-HETrE, thus warranting exploration. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:363 / 372
页数:10
相关论文
共 34 条
[1]
SELECTIVE KILLING OF HUMAN CANCER-CELLS BY POLY-UNSATURATED FATTY-ACIDS [J].
BEGIN, ME ;
DAS, UN ;
ELLS, G ;
HORROBIN, DF .
PROSTAGLANDINS LEUKOTRIENES AND MEDICINE, 1985, 19 (02) :177-186
[2]
ARACHIDONIC-ACID METABOLISM IN BENIGN AND MALIGNANT PROSTATIC TISSUE IN-VITRO - EFFECTS OF FATTY-ACIDS AND CYCLOOXYGENASE INHIBITORS [J].
CHAUDRY, AA ;
WAHLE, KWJ ;
MCCLINTON, S ;
MOFFAT, LEF .
INTERNATIONAL JOURNAL OF CANCER, 1994, 57 (02) :176-180
[3]
γ-linolenic acid in borage oil reverses epidermal hyperproliferation in guinea pigs [J].
Chung, S ;
Kong, S ;
Seong, K ;
Cho, Y .
JOURNAL OF NUTRITION, 2002, 132 (10) :3090-3097
[4]
Incidence of adenocarcinoma of the prostate in Asian immigrants to the United States and their descendants [J].
Cook, LS ;
Goldoft, M ;
Schwartz, SM ;
Weiss, NS .
JOURNAL OF UROLOGY, 1999, 161 (01) :152-155
[5]
Peroxisome proliferator-activated receptor activators inhibit thrombin-induced endothelin-1 production in human vascular endothelial cells by inhibiting the activator protein-1 signaling pathway [J].
Delerive, P ;
Martin-Nizard, F ;
Chinetti, G ;
Trottein, F ;
Fruchart, JC ;
Najib, J ;
Duriez, P ;
Staels, B .
CIRCULATION RESEARCH, 1999, 85 (05) :394-402
[6]
The nuclear eicosanoid receptor, PPARγ, is aberrantly expressed in colonic cancers [J].
DuBois, RN ;
Gupta, R ;
Brockman, J ;
Reddy, BS ;
Krakow, SL ;
Lazar, MA .
CARCINOGENESIS, 1998, 19 (01) :49-53
[7]
15-DEOXY-DELTA(12,14)-PROSTAGLANDIN J(2) IS A LIGAND FOR THE ADIPOCYTE DETERMINATION FACTOR PPAR-GAMMA [J].
FORMAN, BM ;
TONTONOZ, P ;
CHEN, J ;
BRUN, RP ;
SPIEGELMAN, BM ;
EVANS, RM .
CELL, 1995, 83 (05) :803-812
[8]
Inhibition of arachidonate 5-lipoxygenase triggers massive apoptosis in human prostate cancer cells [J].
Ghosh, J ;
Myers, CE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (22) :13182-13187
[9]
Ghosh J, 1998, NUTRITION, V14, P48
[10]
Arachidonic acid stimulates prostate cancer cell growth: Critical role of 5-lipoxygenase [J].
Ghosh, J ;
Myers, CE .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 235 (02) :418-423