Effect of altering dietary ω-6/ω-3 fatty acid ratios on prostate cancer membrane composition, cyclooxygenase-2, and prostaglandin E2

被引:133
作者
Kobayashi, Naoko
Barnard, R. James
Henning, Susanne M.
Elashoff, David
Reddy, Srinivasa T.
Cohen, Pinchas
Leung, Pak
Hong-Gonzalez, Jenny
Freedland, Stephen J.
Said, Jonathan
Gui, Dorina
Seeram, Navindra P.
Popoviciu, Laura M.
Bagga, Dilprit
Heber, David
Glaspy, John A.
Aronson, William J.
机构
[1] Univ Calif Los Angeles, Dept Urol, Ctr Hlth Sci 66 124, Sch Med, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Sch Med, Dept Biostat, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Sch Med, Div Clin Nutr, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, Sch Med, Dept Med, Div Hematol Oncol, Los Angeles, CA 90095 USA
[5] Univ Calif Los Angeles, Sch Med, Dept Pediat, Div Pediat Endocrinol, Los Angeles, CA 90095 USA
[6] Univ Calif Los Angeles, Sch Med, Dept Pathol, Los Angeles, CA 90095 USA
[7] Univ Calif Los Angeles, Dept Physiol Sci, Los Angeles, CA 90095 USA
[8] Vet Adm Greater Los Angeles Healthcare Syst, Dept Surg, Urol Sect, Los Angeles, CA USA
[9] Boston Univ, Sch Med, Boston, MA 02118 USA
[10] Duke Univ, Sch Med, Vet Adm Med Ctr, Dept Surg, Durham, NC USA
[11] Duke Univ, Sch Med, Urol Sect, Dept Surg, Durham, NC USA
[12] Univ Calif Los Angeles, Sch Med, Dept Cardiol, Los Angeles, CA 90095 USA
关键词
NONSTEROIDAL ANTIINFLAMMATORY DRUGS; MESSENGER-RNA; CELL-GROWTH; DOCOSAHEXAENOIC ACID; TUMOR-GROWTH; IN-VITRO; EXPRESSION; RISK; ANGIOGENESIS; INHIBITION;
D O I
10.1158/1078-0432.CCR-06-0459
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To determine whether altering the dietary content of omega-6 (n-6) ando)-3 (n-3) polyunsaturated fatty acids affects the growth of androgen-sensitive prostate cancer xenografts, tumor membrane fatty acid composition, and tumor cyclooxygenase-2 and prostaglandin E-2 (PGE(2)) levels. Experimental Design: Individually caged male severe combined immunodeficiency mice were fed isocaloric 20% kcal fat diets with the fat derived either primarily from n-6 fatty acids (n-6 group) or with the fat consisting of n-6 and n-3 fatty acids in a ratio of 1:1 (n-3 group), and injected s.c. with Los Angeles Prostate Cancer 4 (LAPC-4) cells. Tumor volumes and mouse weights were measured weekly, caloric intake was measured 3 days per week, and tumors and serum were harvested at 8 weeks postinjection. Results: Tumor growth rates, final tumor volumes, and serum prostate-specific antigen levels were reduced in the n-3 group relative to the n-6 group. The n-3 group tumors had decreased proliferation (Ki67 staining) and increased apoptosis (terminal nucleotidyl transferase-mediated nick end labeling staining). In vitro proliferation of LAPC-4 cells in medium containing n-3 group serum was reduced by 22% relative to LAPC-4 cells cultured in medium containing serum from the n-6 group. The n-6/n-3 fatty acid ratios in serum and tumor membranes were lower in the n-3 group relative to the n-6 group. In addition, n-3 group tumors had decreased cyclooxygenase-2 protein and mRNA levels, an 83% reduction in PGE(2) levels, and decreased vascular endothelial growth factor expression. Conclusion: These results provide a sound basis for clinical trials evaluating the effect of dietary n-3 fatty acids from fish oil on tumor PGE(2) and membrane fatty acid composition, and serum and tumor biomarkers of progression in men with prostate cancer.
引用
收藏
页码:4662 / 4670
页数:9
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