• [email protected]
  • +971 507 888 742
Submit Manuscript
SciAlert
  • Home
  • Journals
  • Information
    • For Authors
    • For Referees
    • For Librarian
    • For Societies
  • Contact
  1. International Journal of Cancer Research
  2. Vol 5 (1), 2009
  3. 25-35
  • Issues
    Online First Current Issue All Issues
  • Information About
    Aims and Scope Editorial Board Guide to Authors Article Processing Charges
    Submit a Manuscript

International Journal of Cancer Research

Year: 2009 | Volume: 5 | Issue: 1 | Page No.: 25-35
DOI: 10.3923/ijcr.2009.25.35

Facebook Twitter Reddit Linkedin E-mail
Google Scholar ASCI
Research Article

A Comparison of Rice Bran, Corn Oil and Soybean Oil Against Azoxymethane Induced Colon Cancer in a Fisher 344 Rat Model

V. Panala
Department of Food and Animal Sciences, Alabama A and M University, P.O. Box 1628, Normal, AL 35762, USA

M. Verghese
Department of Food and Animal Sciences, Alabama A and M University, P.O. Box 1628, Normal, AL 35762, USA

J. Boateng
Department of Food and Animal Sciences, Alabama A and M University, P.O. Box 1628, Normal, AL 35762, USA

R. Field
Department of Food and Animal Sciences, Alabama A and M University, P.O. Box 1628, Normal, AL 35762, USA

L. Shackelford
Department of Food and Animal Sciences, Alabama A and M University, P.O. Box 1628, Normal, AL 35762, USA

L.T. Walker
Department of Food and Animal Sciences, Alabama A and M University, P.O. Box 1628, Normal, AL 35762, USA

The objective of this study was to compare the inhibitory effects of Rice bran oil (RBO), Corn oil (CO) and Soybean oil (SBO) at 7% (normal fat level) and 14% (high fat level) on Azoxymethane (AOM) induced Aberrant Crypt Foci (ACF). The long term effect (End Point Tumor (EPT) study) of dietary fat from the above sources on colon cancer in Fisher 344 male rats was determined. In the ACF study 2 groups of F344 rats (4 weeks old) (n = 6) received AIN-93G Control (C) diet containing 7 and 14% Soybean oil (SBO). The remaining groups were assigned treatment diets consisting of 7 and 14% RBO and CO. The rats remained on their respective diets for 13 weeks. Rats in the EPT study were fed a control (AIN-93G) diet with 7% SBO, while the treatment groups were fed diets containing 7% RBO and CO, respectively. At 20 week of age rats in the EPT study were switched to AIN-93Maintenance (M) diets. All rats received 2 s/c injections of AOM at 7 and 8 week of age @ 16 mg kg-1 body weight in saline. At 17 and 45 week of age all rats were killed by CO2 asphyxiation. Total colonic ACF in the rats fed SBO, RBO and CO at 7 and 14% levels ranged from 101-189. In the EPT study, all the rats fed 7% SBO and CO developed tumors (100% tumor incidence) while tumor incidence in the groups fed RBO, was 54% while tumor size (mm) and tumor/Tumor Bearing Rat ratio (TBR) in the rats fed SBO, RBO and CO ranged from 1.3-6.86 and 1.83-5.86, respectively. Present results indicate that the type and constituents (such as n-3 PUFA, vitamin E, phytosterols) of dietary fat plays a significant role in the formation of AOM induced colonic ACF and tumors in Fisher 344 rats.
PDF Fulltext XML References Citation

How to cite this article

V. Panala, M. Verghese, J. Boateng, R. Field, L. Shackelford and L.T. Walker, 2009. A Comparison of Rice Bran, Corn Oil and Soybean Oil Against Azoxymethane Induced Colon Cancer in a Fisher 344 Rat Model. International Journal of Cancer Research, 5: 25-35.

DOI: 10.3923/ijcr.2009.25.35

URL: https://scialert.net/abstract/?doi=ijcr.2009.25.35

Related Articles

Modifying Effects of Pistachio Nuts on Antioxidant Enzymes in Azoxymethane (AOM)-induced Formation of Aberrant Crypt Foci
Experimental Approach to Treatment of Colorectal Cancer by Herbs and Their Constituents: An Overview on in vivo and in vitro Protocols and Molecular Targets

Leave a Comment


Your email address will not be published. Required fields are marked *

Article Trend



Total views 4583

References


  1. Aggarwal, B.B. and S. Shishodia, 2006. Molecular targets of dietary agents for prevention and therapy of cancer. Biochem. Pharmacol., 71: 1397-1421.
    CrossRefPubMedDirect Link

  2. Alabaster, O., Z. Tang and N. Shivpurkar, 1996. Dietary fiber and the Chemo preventive modelation of colon carcinogeneis. Mutat. Res., 3350: 185-197.
    PubMed

  3. Awad, A.B. and C.S. Fink, 2000. Phytosterol as anticancer dietary component: Evidence and Mechanism of action. J. Nutr., 130: 2127-2130.
    PubMed

  4. Abdul-Hamid, A. and Y.S. Luan, 2000. Functional properties of dietary fibre prepared from defatted rice bran. J. Food Chem., 68: 15-19.
    CrossRefDirect Link

  5. Azzi, A., R. Gysin, P. Kempná, A. Munteanu and Y. Negis et al., 2004. Vitamin E mediates cell signaling and regulation of gene expression. Ann. N. Y. Acad. Sci., 1031: 86-95.
    PubMed

  6. Betti, M., A. Minelli, B. Canonico, P. Castaldo and S. Magi et al., 2006. Antiproliferative effects of tocopherols (vitamin E) on murine glioma C6 cells: Homologue-specific control of PKC/ERK and cyclin signaling. Free Radic. Biol. Med., 41: 464-472.
    PubMed

  7. Bird, R.P., 1987. Observation and quantification of aberrant crypts in the murine colon treated with a colon carcinogen: Preliminary findings. Cancer Lett., 37: 147-151.
    PubMed

  8. Bommareddy, A., B.L. Arasada, D.P. Mathees and C. Dwivedi, 2006. Chemopreventive effects of dietary flaxseed on colon tumor development. Nutr. Cancer, 54: 216-222.
    PubMed

  9. Carroll, K.K., 1992. Dietary fat and breast. Cancer, 27: 793-797.
    PubMed

  10. Corpet, D.E. and F. Pierre, 2003. Point: From animal models to prevention of colon cancer. Systematic review of chemoprevention in min mice and choice of the model system. Cancer Epidemiol. Biomarkers Prevent., 12: 391-400.
    PubMed

  11. Doll, R. and R. Peto, 1981. The causes of cancer: quantitative estimates of avoidable risks of cancer in the United States today. J. Natl. Cancer Inst., 66: 1191-1308.
    PubMed

  12. Dommels, Y.E., S. Heemskerk, H. van den Berg, G.M. Alink, P.J. van Bladeren and B. van Ommen, 2003. Effects of high fat fish oil and high fat corn oil diets on initiation of AOM-induced colonic aberrant crypt foci in male F344 rats. Food Chem. Toxicol., 41: 1739-1747.
    PubMed

  13. Dunn, S.E., R.A. Hardman, F.W. Kari and J.C. Barrett, 1997. Insulin-like growth factor 1 (IGF-1) alters drug sensitivity of HBL100 human breast cancer cells by inhibition of apoptosis induced by diverse anticancer drugs. Cancer Res., 57: 2687-2693.
    PubMed

  14. Dunn, S.E., F.W. Kari, J. French, J.R. Leininger, G. Travlos, R. Wilson and J.C. Barrett, 1997. Dietary restriction reduces insulin-like growth factor I. Levels, which modulates apoptosis, cell proliferation and tumor progression in p53-deficient mice. Cancer Res., 57: 4667-4672.
    PubMed

  15. Ghoneum, M. and S. Gollapudi, 2003. Modified arabinoxylan rice bran (MGN-3/Biobran) sensitizes human T cell leukemia cells to death receptor (CD95)-induced apoptosis. Cancer Lett., 201: 41-49.
    PubMed

  16. Guthrie, N., A. Gapor, A.F. Chambers and K.K. Carroll, 1997. Inhibition of proliferation of estrogen receptor-negative MDA-MB-435 and-positive MCF-7 human breast cancer cells by palm oil tocotrienols and tamoxifen, alone and in combination. J. Nutr., 127: 544S-548S.
    PubMed

  17. Habig, W.H., M.J. Pabst and W.B. Jakoby, 1974. Glutathione S-transferases: The first enzymatic step in mercapturic acid formation. J. Biol. Chem., 249: 7130-7139.
    CrossRefPubMedDirect Link

  18. Hughes, J.S., C. Ganthavorn and S. Wilson-Sanders, 1997. Dry beans inhibit azoxymethane-induced colon carcinogenesis in F344 rats. J. Nutr., 127: 2328-2333.
    PubMed

  19. Jacobs, D.R. Jr. and L.M. Steffen, 2003. Nutrients, foods and dietary patterns as exposures in research: A framework for food synergy. Am. J. Clin. Nutr., 78: 508S-513S.
    PubMed

  20. Jones, J.I. and D.R. Clemmons, 1995. Insulin-like growth factors and their binding proteins: Biological actions. Endocrinol. Rev., 16: 3-34.
    PubMed

  21. Juan, P., M. Esther, J. Maria, F.G. Juan, C.T. Laura and B. Juan, 2006. Preparation of rice bran enzymatic extract with potential uses as functional food. Food Chem., 98: 742-748.
    CrossRef

  22. Khandwala, H.M., I.E. McCutcheon, A. Flyvbjerg and K.E. Friend, 2000. The effects of insulin-like growth factors on tumorigenesis and neoplastic growth. Endocr. Rev., 21: 215-244.
    PubMed

  23. Khatiwada, J., M. Verghese, L.T. Walker, L. Shackelford, C.B. Chawan and R. Sunkara, 2006. Combination of green tea, phytic acid, and inositol reduced the incidence of azoxymethane-induced colon tumors in Fisher 344 male rats. LWT Food Sci. Technol., 39: 1080-1086.
    CrossRefDirect Link

  24. Koushik, A., D.J. Hunter, D. Spiegelman, W.L. Beeson and P.A. Van-Den-Brandt et al., 2007. Fruits, vegetables and colon cancer risk in a pooled analysis of 14 cohort studies. J. Natl. Cancer Inst., 99: 1471-1483.
    CrossRefPubMedDirect Link

  25. Lorraine, L.N. and N.N. Suh, 2003. Role on non-digetable carbhohydrates in colon cancer protection. J. Nutr. Food Sci., 33: 28-33.
    CrossRef

  26. McIntosh, G.H. and R.K. Le-Leu, 2001. The influence of dietary proteins on colon cancer risk. Nutr. Res., 21: 1053-1066.
    PubMed

  27. Narisawa, T., M. Takahashi, H. Kotanagi, H. Kusaka and Y. Yamazaki et al., 1991. Inhibitory effect of dietary perilla oil rich in the n-3 polyunsaturated fatty acid alpha-linolenic acid on colon carcinogenesis in rats. Jap. J. Cancer Res., 82: 1089-1096.
    PubMed

  28. Nesaretnam, K., R. Stephen, R. Dils and P. Darbre, 1998. Tocotrienols inhibit the growth of human breast cancer cells irrespective of estrogen receptor status. Lipids, 35: 461-469.
    PubMed

  29. Nesaretnam, K., A. Radhakrishnan, K.R. Selvaduray, K. Reimann and J. Pailoor et al., 2002. Effect of palm oil carotene on breast cancer tumorigenicity in nude mice. Lipids, 37: 557-560.
    PubMed

  30. O'Leary, K.A., S. De-Pascual-Tereasa, P.W. Needs, Y.P. Bao, N.M. O'Brien and G. Williamson, 2004. Effect of flavonoids and vitamin E on cyclooxygenase-2 (COX-2) transcription. Mutat. Res., 551: 245-254.
    CrossRefPubMed

  31. Park, Y., D.J. Hunter, D. Spiegelman, L. Bergkvist and F. Berrino et al., 2005. Dietary fiber intake and risk of colorectal cancer: A pooled analysis of prospective cohort studies. J. Am. Med. Assoc., 294: 2849-2857.
    PubMed

  32. Philip, G.R, H.N. Forrest and C.F. George Jr., 1993. AIN-93 purified diets for laboratory rodents: Final report of the American Institute of Nutrition ad hoc Writing Committee on the Reformulation of the AIN-76A Rodent Diet. J. Nutr., 123: 1939-1951.
    CrossRefPubMedDirect Link

  33. Reeves, P.G., K.L. Rossow and J. Lindlauf, 1993. Development and testing of the AIN-93 purified diets for rodents: Results on growth, kidney calcification and bone mineralization in rats and mice. J. Nutr., 123: 1923-1931.
    PubMedDirect Link

  34. Se-Young, O., H.L. Ji, K.J. Dong, C.H. Seung and J.K. Hyo, 2005. Relationship of nutrients and food to colorectal cancer risk in Koreans. Nutr. Res., 25: 805-819.
    CrossRef

  35. Singh, J., R. Hamid and B.S. Reddy, 1997. Dietary fat and colon cancer modulation of cyclooxygenase-2 by types and amount of dietary fat during the postinitiation stage of colon carcinogenesis. Cancer Res., 57: 3465-3470.
    PubMed

  36. Shackelford, L.A., D.R. Rao, C.B. Chawan and S.R. Pulusani, 1983. Effect of feeding fermented milk on the incidence of chemically induced colon tumors in rats. Nutr. Cancer, 5: 159-164.
    PubMed

  37. Takahashi, M., M. Fukutake, T. Isoi, K. Fukuda and H. Sato et al., 1997. Suppression of azoxymethane-induced rat colon carcinoma development by a fish oil component, docosahexaenoic acid (DHA). Carcinogenesis, 18: 1337-1342.
    PubMed

  38. Traber, M.G., 2005. Vitamin E regulation. Curr. Opin. Gastroenterol., 22: 223-227.
    PubMed

  39. Van-Beelen, V.A., J.M. Aarts, A. Reus, H. Mooibroek and L. Sijtsma et al., 2006. Differential induction of electrophile-responsive element-regulated genes by n-3 and n-6 polyunsaturated fatty acids. FEBS Lett., 580: 4587-4590.
    PubMed

  40. Verghese, M., D.R. Rao, C.B. Chawan and L. Shackelford, 2002. Dietary inulin suppresses azoxymethane-induced preneoplastic aberrant crypt foci in mature fisher 344 rats. J. Nutr., 132: 2804-2808.
    PubMed

  41. Verghese, M., D.R. Rao, C.B. Chawan, L.L. Williams and L. Shackelford, 2002. Dietary inulin suppresses azoxymethane-induced aberrant crypt foci and colon tumors at the promotion stage in young fisher 344 rats. J. Nutr., 132: 2809-2813.
    PubMedDirect Link

  42. Williams, D., M. Verghese, L.T. Walker, J. Boateng, L. Shackelford and C.B. Chawan, 2007. Flax seed oil and flax seed meal reduce the formation of Aberrant Crypt Foci (ACF) in azoxymethane-induced colon cancer in Fisher 344 male rats. Food Chem. Toxicol., 45: 153-159.
    PubMedDirect Link

  43. Zhang, W., W.H. Thornton and R.S. MacDonald, 1998. Insulin-like growth factor-I and II receptor expression in rat colon mucosa are affected by dietary lipid intake. J. Nutr., 128: 158-165.
    PubMed

  44. Zoran, D.L., N.D. Turner, S.S. Taddeo, R.S. Chapkin and J.R. Lupton, 1997. Wheat bran diet reduces tumor incidence in a rat model of colon cancer independent of effects on distal luminal butyrate concentrations. J. Nutr., 127: 2217-2225.
    PubMed

  45. Boateng, J., M. Verghese, C.B. Chawan, L. Shackelford, L.T. Walker, J. Khatiwada and D.S. Williams, 2006. Red palm oil suppresses the formation of azoxymethane (AOM) induced aberrant crypt foci (ACF) in fisher 344 male rats. Food Chem. Toxicol., 44: 1667-1673.
    CrossRefPubMedDirect Link

Keywords


  • dietary fat
  • Fisher rat model
  • corn oil
  • rice bran oil
  • azoxymethane
  • Colon cancer

Useful Links

  • Journals
  • For Authors
  • For Referees
  • For Librarian
  • For Socities

Contact Us

Office Number 1128,
Tamani Arts Building,
Business Bay,
Deira, Dubai, UAE

Phone: +971 507 888 742
Email: [email protected]

About Science Alert

Science Alert is a technology platform and service provider for scholarly publishers, helping them to publish and distribute their content online. We provide a range of services, including hosting, design, and digital marketing, as well as analytics and other tools to help publishers understand their audience and optimize their content. Science Alert works with a wide variety of publishers, including academic societies, universities, and commercial publishers.

Follow Us
© Copyright Science Alert. All Rights Reserved