Among dietary factors, there is strong epidemiological, clinical and experimental data indicating a protective effect on n-3 polyunsaturated fatty acids (n-3 PUFAs; eicosapentaenoic acid, 20:5n- 3 and docosahexaenoic acid, 22:n-3) on colon cancer. We have recently demonstrated that dietary n-3 PUFAs confer protection against experimental carcinogenesis, i.e., a reduction in tumor incidence, in part by enhancing the deletion of cells through activation of apoptosis, which may reduce the accumulation of genetic errors. These data support our postulate that dietary n-3 PUFAs act as anticarcinogens by facilitating the apoptotic removal of carcinogen adducted cells. In order to further elucidate the mechanism(s) by which n-3 PUFAs-induce apoptosis. We will utilize the highly relevant rat model of colon carcinogenesis to determine whether n-3 PUFAs modulate DNA adduct formation, removal (DNA repair) and/or deletion (apoptosis) during the initial stages of malignant transformation. We have also recently show that n-3 PUFAs prevent the carcinogen-induced chronic down-regulation of colonic protein kinase C (PKC) delta (novel), zeta (atypical), and the selective up- regulation of PKC betaII (classical). This is significant because the maintenance of crypt PKC levels may sustain the homeostatic balance between cell proliferation and apoptosis. Therefore, we have hypothesized that n-3 PUFAs reduce colon cancer incidence in part by blocking the effects of carcinogen on colonic PKC isozyme-related signal transduction. To further determine the significance of n-3 PUFA-induced changes in colonic PKC expression, we will elucidate the role of specific PKC isozymes in colon tumor development by using a targeted pharmacological inhibitor in vivo in combination with overepression and antisense strategies in vitro. Elucidation of the mechanism(s) by which dietary n-3 PUFAs reduce colon cancer incidence will lead to the establishment of dietary guidelines designed to reduce colon cancer morbidity and mortality. This experimental approach is particularly relevant because despite advancement in the treatment of colon cancer, the 5 year mortality rate has not appreciable improved over the past 4 decades. Therefore, chemopreventive dietary strategies must be developed in order to decrease the risk of colon cancer.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
2R01CA059034-04A1
Application #
2697556
Study Section
Metabolic Pathology Study Section (MEP)
Program Officer
Seifried, Harold E
Project Start
1994-12-23
Project End
2003-04-30
Budget Start
1998-08-05
Budget End
1999-04-30
Support Year
4
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Texas A&M University
Department
Veterinary Sciences
Type
Schools of Earth Sciences/Natur
DUNS #
047006379
City
College Station
State
TX
Country
United States
Zip Code
77845
Monk, Jennifer M; Turk, Harmony F; Fan, Yang-Yi et al. (2014) Antagonizing arachidonic acid-derived eicosanoids reduces inflammatory Th17 and Th1 cell-mediated inflammation and colitis severity. Mediators Inflamm 2014:917149
Cho, Youngmi; Turner, Nancy D; Davidson, Laurie A et al. (2014) Colon cancer cell apoptosis is induced by combined exposure to the n-3 fatty acid docosahexaenoic acid and butyrate through promoter methylation. Exp Biol Med (Maywood) 239:302-10
Turk, Harmony F; Monk, Jennifer M; Fan, Yang-Yi et al. (2013) Inhibitory effects of omega-3 fatty acids on injury-induced epidermal growth factor receptor transactivation contribute to delayed wound healing. Am J Physiol Cell Physiol 304:C905-17
Turk, Harmony F; Chapkin, Robert S (2013) Membrane lipid raft organization is uniquely modified by n-3 polyunsaturated fatty acids. Prostaglandins Leukot Essent Fatty Acids 88:43-7
Monk, Jennifer M; Kim, Wooki; Callaway, Evelyn et al. (2012) Immunomodulatory action of dietary fish oil and targeted deletion of intestinal epithelial cell PPAR? in inflammation-induced colon carcinogenesis. Am J Physiol Gastrointest Liver Physiol 302:G153-67
Monk, Jennifer M; Hou, Tim Y; Turk, Harmony F et al. (2012) Dietary n-3 polyunsaturated fatty acids (PUFA) decrease obesity-associated Th17 cell-mediated inflammation during colitis. PLoS One 7:e49739
Monk, Jennifer M; Jia, Qian; Callaway, Evelyn et al. (2012) Th17 cell accumulation is decreased during chronic experimental colitis by (n-3) PUFA in Fat-1 mice. J Nutr 142:117-24
Cho, Youngmi; Turner, Nancy D; Davidson, Laurie A et al. (2012) A chemoprotective fish oil/pectin diet enhances apoptosis via Bcl-2 promoter methylation in rat azoxymethane-induced carcinomas. Exp Biol Med (Maywood) 237:1387-93
Hou, Tim Y; Monk, Jennifer M; Fan, Yang-Yi et al. (2012) n-3 polyunsaturated fatty acids suppress phosphatidylinositol 4,5-bisphosphate-dependent actin remodelling during CD4+ T-cell activation. Biochem J 443:27-37
Shah, Manasvi S; Davidson, Laurie A; Chapkin, Robert S (2012) Mechanistic insights into the role of microRNAs in cancer: influence of nutrient crosstalk. Front Genet 3:305

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