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Nutritional–pharmacological combinations

A novel approach to reducing colon cancer incidence

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European Journal of Nutrition Aims and scope Submit manuscript

Summary

Background

Recent studies have suggested that n–9 fatty acids in olive oil prevent colon carcinogenesis while n–6 PUFA seems to activate this process.

Aims

To evaluate the effects of nutritional–pharmacological combinations made up of olive or soy oilbased diets and the drug sulindac, on colon cancer incidence in a chemically induced (1,2–dimethylhydrazine, DMH) rat cancer model.

Methods

Male rats were assigned to two different dietary regimes based on a standard murine defined diet (AIN–76A) containing either a low (4%) or high (15 %) concentration of olive or soy oil. Some groups also received sulindac in their food (80 mg/kg food) starting from the ninth week following the first DMH or vehicle administration.

Results

Oleic and linoleic acid reached higher levels in plasma and liver lipids when rats were fed high concentrations of olive or soy oil, respectively. Rats fed a low or high soy oil–based diet showed no significant difference in the number of aberrant crypt foci (ACF) in proximal or distal colon specimens. In contrast, rats fed a higher olive oil–based diet developed a significantly lower number of ACF than rats fed a low concentration of olive oil. Addition of sulindac reduced the number of ACF in rats fed the 4%, but not the 15%, soy oil diet. In contrast, the effect of sulindac was significant when combined with both the low and high concentrations of olive oil. High soy oilbased diet or DMH treatment upregulated colon expression of Bcl–2, but not that of cyclooxygenase–2 (COX–2). In contrast, olive oil dose–dependently downregulated the expression of both Bcl–2 and COX–2 in colonic mucosa and also abrogated the upregulation of Bcl–2 by DMH. Olive oil/sulindac combinations were effective in downregulating colonic mucosa Bcl–2 expression (with the 4% oil diet) and COX–2 expression (with the 15% oil diet). These effects were not observed in rats fed the soy oil/sulindac combinations. Caspase–3 activity in colonic mucosa was unaffected by soy oil or soy oil/sulindac combinations. The addition of olive oil, on the other hand, significantly enhanced colonic caspase–3 activity.

Conclusions

Diets containing high levels of olive oil exert a significant protective effect from tumor development that is additive with the inhibitory effect of sulindac. These inhibitory effects are mediated by regulating the expression and activity of key proteins involved in prostaglandin–biosynthesis and apoptosis–induction pathways. It may be concluded that appropriate dietary–pharmacological combination can improve anti–tumor efficacy over either dietary or pharmacological intervention alone.

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Abbreviations

ACF:

aberrant crypt foci

Cox–2:

cyclooxygenase–2

DMH:

1,2–1,2–dimethylhydrazine

NSAID:

non–steroidal anti–inflammatory drug

PUFA:

polyunsaturated fatty acid

References

  1. Grady WM, Markowitz SD (2002) Genetic and epigenetic alterations in colon cancer. Annu Rev Genomics Hum Genet 3:101–128

    CAS  PubMed  Google Scholar 

  2. Augenlicht LH, Heerdt BG, Mariadason JM, Yang W, Wilson AJ, Fragale A, Velcich A (2002) Environment-gene interactions in intestinal cancer. Eur J Cancer Prev 11:S12–S17

    PubMed  Google Scholar 

  3. Dommels YE,Alink GM, Linssen JP, van Ommen B (2002) Effects of n-6 and n-3 polyunsaturated fatty acids on gap junctional intercellular communication during spontaneous differentiation of the human colon adenocarcinoma cell line Caco-2. Nutr Cancer 42:125–130

    Article  CAS  PubMed  Google Scholar 

  4. Boudreau MD, Sohn KH, Rhee SH, Lee SW, Hunt JD, Hwang DH (2001) Suppression of tumor cell growth both in nude mice and in culture by n-3 polyunsaturated fatty acids: mediation through cyclooxygenase-independent pathways. Cancer Res 61:1386–1391

    CAS  PubMed  Google Scholar 

  5. Hong MY, Lupton JR, Morris JS, Wang N, Carroll RJ, Davidson LA, Elder RH, Chapkin RS (2000) Dietary fish oil reduces O6-methylguanine DNA adduct levels in rat colon in part by increasing apoptosis during tumor initiation. Cancer Epidemiol Biomarkers Prev 8:819–826

    Google Scholar 

  6. Gatof D, Ahnen D (2002) Primary prevention of colorectal cancer: diet and drugs. Gastroenterol Clin North Am 2:587–623

    Google Scholar 

  7. Slattery ML,Curtin K,Ma K,Edwards S, Schaffer D, Anderson K, Samowitz W (2002) Diet activity,and lifestyle associations with p53 mutations in colon tumors. Cancer Epidemiol Biomarkers Prev 6:541–548

    Google Scholar 

  8. Koornstra JJ, de Jong S, Hollema H, de Vries EG,Kleibeuker JH (2003) Changes in apoptosis during the development of colorectal cancer: a systematic review of the literature. Crit Rev Oncol Hematol 45:37–53

    Article  CAS  PubMed  Google Scholar 

  9. Avivi-Green C,Polak-Charcon S,Madar Z, Schwartz B (2002) Different molecular events account for butyrate-induced apoptosis in two human colon cancer cell lines. J Nutr 132:1812–1818

    CAS  PubMed  Google Scholar 

  10. Rao CV,Hirose Y, Indranie C, Reddy BS (2001) Modulation of experimental colon tumorigenesis by types and amounts of dietary fatty acids. Cancer Res 61:1927–1933

    CAS  PubMed  Google Scholar 

  11. Zock PL (2001) Dietary fats and cancer. Curr Opin Lipidol 12:5–10

    Article  CAS  PubMed  Google Scholar 

  12. Bartoli R, Fernandez-Banares F, Navarro E, Castella E, Mane J, Alvarez M, Pastor C, Cabre E, Gassull MA (2000) Effect of olive oil on early and late events of colon carcinogenesis in rats: modulation of arachidonic acid metabolism and local prostaglandin E2 synthesis. Gut 46:191–199

    Article  CAS  PubMed  Google Scholar 

  13. Hardman WE (2002) Omega-3 fatty acids to augment cancer therapy. J Nutr 132:3508S–3512S

    CAS  PubMed  Google Scholar 

  14. Song JH, Fujimoto K, Miyazawa T (2000) Polyunsaturated (n-3) fatty acids susceptible to peroxidation are increased in plasma and tissue lipids of rats fed docosahexaenoic acid-containing oils. J Nutr 130:3028–3033

    CAS  PubMed  Google Scholar 

  15. Mori TA, Puddey IB, Burke V, Croft KD, Dunstan DW, Rivera JH, Beilin LJ (2000) Effect of omega 3 fatty acids on oxidative stress in humans: GC-MS measurement of urinary F2-isoprostane excretion. Redox Rep 5:45–46

    CAS  PubMed  Google Scholar 

  16. Kratz M, von Eckardstein A, Fobker M, Buyken A, Posny N, Schulte H, Assmann G, Wahrburg U (2002) The impact of dietary fat composition on serum leptin concentrations in healthy nonobese men and women. J Clin Endocrinol Metab 87:5008–5014

    CAS  PubMed  Google Scholar 

  17. Kato T, Hancock RL, Mohammadpour H, McGregor B, Manalo P, Khaiboullina S, Hall MR, Pardini L, Pardini RS (2002) Influence of omega-3 fatty acids on the growth of human colon carcinoma in nude mice. Cancer Lett 187:169–177

    Article  CAS  PubMed  Google Scholar 

  18. Ntambi JM, Bene H (2001) Polyunsaturated fatty acid regulation of gene expression. J Mol Neurosci 16:273–278

    Article  CAS  PubMed  Google Scholar 

  19. Pai R, Soreghan B, Szabo IL, Pavelka M, Baatar D, Tarnawski AS (2002) Prostaglandin E2 transactivates EGF receptor: a novel mechanism for promoting colon cancer growth and gastrointestinal hypertrophy. Nat Med 3:289–293

    Article  Google Scholar 

  20. Tapiero H, Ba GN, Couvreur P, Tew KD (2002) Polyunsaturated fatty acids (PUFA) and eicosanoids in human health and pathologies. Biomed Pharmacother 56:215–222

    Article  CAS  PubMed  Google Scholar 

  21. Turini ME, DuBois RN (2002) Cyclooxygenase- 2: a therapeutic target. Annu Rev Med 53:35–57

    Article  CAS  PubMed  Google Scholar 

  22. Rice PL, Washington M, Schleman S, Beard KS, Driggers LJ, Ahnen DJ (2003) Sulindac sulfide inhibits epidermal growth factor-induced phosphorylation of extracellular-regulated kinase 1/2 and Bad in human colon cancer cells. Cancer Res 63:616–620

    CAS  PubMed  Google Scholar 

  23. Giardiello FM, Yang VW, Hylind LM, Krush AJ, Petersen GM, Trimbath JD, Piantadosi S, Garrett E, Geiman DE, Hubbard W, Offerhaus GJ, Hamilton SR (2002) Primary chemoprevention of familial adenomatous polyposis with sulindac. N Engl J Med 346:1054–1059

    Article  CAS  PubMed  Google Scholar 

  24. Schwartz B, Avivi C, Lamprecht SA (1991) Isolation and characterization of normal and neoplastic colonic epithelial cell populations. Gastroenterology 100:692–702

    CAS  PubMed  Google Scholar 

  25. Friedman A, Sklan D (1995) Effect of dietary fatty acids on antibody production and fatty acid composition of lymphoid organs in broiler chicks. Poult Sci 74:1463–1469

    CAS  PubMed  Google Scholar 

  26. Avivi-Green C, Polak-Charcon S, Madar Z, Schwartz B (2000) Dietary regulation and localization of apoptosis cascade proteins in the colonic crypt. J Cell Biochem 77:18–29

    CAS  PubMed  Google Scholar 

  27. Avivi-Green C, Polak-Charcon S, Madar Z, Schwartz B (2002) Different molecular events account for butyrate-induced apoptosis in two human colon cancer cell lines. J Nutr 132:1812–1818

    CAS  PubMed  Google Scholar 

  28. Avivi-Green C, Polak-Charcon S, Madar Z, Schwartz B (2000) Apoptosis cascade proteins are regulated in vivo by high intracolonic butyrate concentration: correlation with colon cancer inhibition. Oncol Res 12:83–95

    CAS  PubMed  Google Scholar 

  29. Avivi-Green C, Madar Z, Schwartz B (2000) Pectin-enriched diet affects distribution and expression of apoptosiscascade proteins in colonic crypts of dimethylhydrazine- treated rats. Int J Mol Med 6:689–698

    CAS  PubMed  Google Scholar 

  30. Slattery ML, Curtin K, Anderson K, Ma KN, Edwards S, Leppert M, Potter J, Schaffer D, Samowitz WS (2000) Associations between dietary intake and Ki-ras mutations in colon tumors: a population-based study. Cancer Res 60:6935–6941

    CAS  PubMed  Google Scholar 

  31. Franceschi S (1999) Nutrients and food groups and large bowel cancer in Europe. Eur J Cancer Prev 8:S49–S52

    PubMed  Google Scholar 

  32. Guthrie N, Carroll KK (1999) Specific versus non-specific effects of dietary fat on carcinogenesis. Prog Lipid Res 38:261–271

    Article  CAS  PubMed  Google Scholar 

  33. Potter JD (1996) Nutrition and colorectal cancer. Cancer Causes Control 1:127–146

    Google Scholar 

  34. Bartsch H, Nair J, Owen RW (1999) Dietary polyunsaturated fatty acids and cancers of the breast and colorectum: emerging evidence for their role as risk modifiers. Carcinogenesis 20: 2209–2218

    Article  CAS  PubMed  Google Scholar 

  35. Kossoy G, Yarden G, Ben-Hur H, Kossoy N, Stark A, Madar Z, Zusman I (2001) Comparative effects of dimethylbenz( a)anthacene and a 15 % olive-oil diet on cellular components and expression of apoptosis-related proteins in the spleen and mammary gland tumors of rats. Oncol Rep 8:435–439

    CAS  PubMed  Google Scholar 

  36. Bernstein H, Holubec H, Warneke JA, Garewal H, Earnest DL, Payne CM, Roe DJ, Cui H, Jacobson EL, Bernstein C (2002) Patchy field defects of apoptosis resistance and dedifferentiation in flat mucosa of colon resections from colon cancer patients. Ann Surg Oncol 9:505–517

    Article  PubMed  Google Scholar 

  37. Chan AO, Broaddus RR, Houlihan PS, Issa JP, Hamilton SR, Rashid A (2002) CpG island methylation in aberrant crypt foci of the colorectum. Am J Pathol 160:1823–1830

    CAS  PubMed  Google Scholar 

  38. Owen RW, Mier W, Giacosa A, Hull WE, Spiegelhalder B, Bartsch H (2000) Phenolic compounds and squalene in olive oils: the concentration and antioxidant potential of total phenols, simple phenols, secoiridoids, lignans and squalene. Food Chem Toxicol 38:647–659

    Article  CAS  PubMed  Google Scholar 

  39. Budiyanto A, Ahmed NU,Wu A, Bito T, Nikaido O, Osawa T, Ueda M, Ichihashi M (2000) Protective effect of topically applied olive oil against photocarcinogenesis following UVB exposure of mice. Carcinogenesis 21:2085–2090

    Article  CAS  PubMed  Google Scholar 

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Correspondence to B. Schwartz Ph. D..

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Schwartz, B., Birk, Y., Raz, A. et al. Nutritional–pharmacological combinations. Eur J Nutr 43, 221–229 (2004). https://doi.org/10.1007/s00394-004-0462-6

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  • DOI: https://doi.org/10.1007/s00394-004-0462-6

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