Abstract
Male C57BL/65 mice received a basal diet supplemented with 4% soya-bean oil, linseed oil or fish oil, in which the major polyunsaturated fatty acids were linoleic acid, alpha-linolenic acid and long chain omega-3 fatty acids, respectively. Groups of animals were injected into the right flank with EL4-lymphoma cells, others with thymoma cells. Tumour implantation caused a gradual decrease in food consumption with both types of tumour, while body weight increased, especially in the EL4-bearing animals receiving the soya-bean diet. The weight gain was due to body water accumulation and was accompanied by decreases in body fat and minor changes in carcass protein and ash contents. The dietary treatments did not produce significant differences in tumour incidence and mortality, but tumour size was decreased by diets supplying omega-3 fatty acids: in the EL4 mice tumour weight was markedly depressed by linseed oil, compared to soya-bean oil, whereas thymoma tumour weight was lowest in mice receiving fish oil and highest in the soya-bean oil group. Both types of tumour caused pronounced hypoglycaemia and hyperinsulinaemia in the hosts, and the effect was modulated by the diets in the EL4 but not in the thymoma animals: the plasma glucose level was especially low in the linseed oil group and relatively highest in the soya-bean oil treatment. The degree of hyperinsulinaemia depended on the diet only in the thymoma-bearing mice, with linseed and fish oils producing higher insulin levels than soya-bean oil. A slight hyperinsulinaemia was also observed in linseed and fish oil-fed control mice. Serum triglycerides were elevated in tumour-bearing animals, without consistent differences between dietary treatments. Although no clear pattern emerged concerning total cholesterol and LDL levels, HDL values were strongly affected by the type of oil: in the control animals linseed oil caused an increase in HDL-cholesterol compared to the other two oils. The thymoma-bearing mice responded to the linseed and fish oil diets with greatly elevated HDL-cholesterol levels. The results point to important differences in the responses of the two implanted tumours and hosts not only to the omega-6 and omega-3 fatty acids, but also to the type of dietary omega-3 fatty acids, namely alpha-linolenic acid and long chain fish oil polyunsaturated fatty acids.
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Selected References
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- Beck S. A., Tisdale M. J. Production of lipolytic and proteolytic factors by a murine tumor-producing cachexia in the host. Cancer Res. 1987 Nov 15;47(22):5919–5923. [PubMed] [Google Scholar]
- Bibby M. C., Double J. A., Ali S. A., Fearon K. C., Brennan R. A., Tisdale M. J. Characterization of a transplantable adenocarcinoma of the mouse colon producing cachexia in recipient animals. J Natl Cancer Inst. 1987 Mar;78(3):539–546. [PubMed] [Google Scholar]
- Braden L. M., Carroll K. K. Dietary polyunsaturated fat in relation to mammary carcinogenesis in rats. Lipids. 1986 Apr;21(4):285–288. doi: 10.1007/BF02536414. [DOI] [PubMed] [Google Scholar]
- Carroll K. K., Braden L. M. Dietary fat and mammary carcinogenesis. Nutr Cancer. 1984;6(4):254–259. doi: 10.1080/01635588509513831. [DOI] [PubMed] [Google Scholar]
- Carroll K. K., Hopkins G. J. Dietary polyunsaturated fat versus saturated fat in relation to mammary carcinogenesis. Lipids. 1979 Feb;14(2):155–158. doi: 10.1007/BF02533866. [DOI] [PubMed] [Google Scholar]
- Carter C. A., Milholland R. J., Shea W., Ip M. M. Effect of the prostaglandin synthetase inhibitor indomethacin on 7,12-dimethylbenz(a)anthracene-induced mammary tumorigenesis in rats fed different levels of fat. Cancer Res. 1983 Aug;43(8):3559–3562. [PubMed] [Google Scholar]
- Cohen N. D., Hilf R. Influence of insulin on estrogen-induced responses in the r3230ac mammary carcinoma. Cancer Res. 1975 Mar;35(3):560–567. [PubMed] [Google Scholar]
- Cohen N. D., Hilf R. Influence of insulin on growth and metabolism of 7,12-dimethylbenz(alpha)anthracene-induced mammary tumors. Cancer Res. 1974 Dec;34(12):3245–3252. [PubMed] [Google Scholar]
- Culp B. R., Titus B. G., Lands W. E. Inhibition of prostaglandin biosynthesis by eicosapentaenoic acid. Prostaglandins Med. 1979 Nov;3(5):269–278. doi: 10.1016/0161-4630(79)90068-5. [DOI] [PubMed] [Google Scholar]
- Feldman J. M., Hilf R. A role of estrogens and insulin binding in the dietary lipid alteration of R3230AC mammary carcinoma growth in rats. Cancer Res. 1985 May;45(5):1964–1972. [PubMed] [Google Scholar]
- Fossati P., Prencipe L. Serum triglycerides determined colorimetrically with an enzyme that produces hydrogen peroxide. Clin Chem. 1982 Oct;28(10):2077–2080. [PubMed] [Google Scholar]
- Goodnight S. H., Jr, Harris W. S., Connor W. E., Illingworth D. R. Polyunsaturated fatty acids, hyperlipidemia, and thrombosis. Arteriosclerosis. 1982 Mar-Apr;2(2):87–113. doi: 10.1161/01.atv.2.2.87. [DOI] [PubMed] [Google Scholar]
- Haran-Ghera N., Ben-Yaakov M., Peled A. Immunologic characteristics in relation to high and low leukemogenic activity of radiation leukemia virus variants. I. Cellular analysis of immunosuppression. J Immunol. 1977 Feb;118(2):600–606. [PubMed] [Google Scholar]
- Hartog J. M., Lamers J. M., Montfoort A., Becker A. E., Klompe M., Morse H., ten Cate F. J., van der Werf L., Hülsmann W. C., Hugenholtz P. G. Comparison of mackerel-oil and lard-fat enriched diets on plasma lipids, cardiac membrane phospholipids, cardiovascular performance, and morphology in young pigs. Am J Clin Nutr. 1987 Aug;46(2):258–266. doi: 10.1093/ajcn/46.2.258. [DOI] [PubMed] [Google Scholar]
- Hillyard L. A., Abraham S. Effect of dietary polyunsaturated fatty acids on growth of mammary adenocarcinomas in mice and rats. Cancer Res. 1979 Nov;39(11):4430–4437. [PubMed] [Google Scholar]
- Hopkins G. J., Kennedy T. G., Carroll K. K. Polyunsaturated fatty acids as promoters of mammary carcinogenesis induced in Sprague-Dawley rats by 7,12-dimethylbenz[a]anthracene. J Natl Cancer Inst. 1981 Mar;66(3):517–522. [PubMed] [Google Scholar]
- Hori T., Moriuchi A., Okuyama H., Sobajima T., Tamiya-Koizumi K., Kojima K. Effect of dietary essential fatty acids on pulmonary metastasis of ascites tumor cells in rats. Chem Pharm Bull (Tokyo) 1987 Sep;35(9):3925–3927. doi: 10.1248/cpb.35.3925. [DOI] [PubMed] [Google Scholar]
- Hubbard N. E., Erickson K. L. Enhancement of metastasis from a transplantable mouse mammary tumor by dietary linoleic acid. Cancer Res. 1987 Dec 1;47(23):6171–6175. [PubMed] [Google Scholar]
- Jurkowski J. J., Cave W. T., Jr Dietary effects of menhaden oil on the growth and membrane lipid composition of rat mammary tumors. J Natl Cancer Inst. 1985 May;74(5):1145–1150. [PubMed] [Google Scholar]
- Karmali R. A., Marsh J., Fuchs C. Effect of omega-3 fatty acids on growth of a rat mammary tumor. J Natl Cancer Inst. 1984 Aug;73(2):457–461. doi: 10.1093/jnci/73.2.457. [DOI] [PubMed] [Google Scholar]
- Lardinois C. K., Starich G. H., Mazzaferri E. L., DeLett A. Polyunsaturated fatty acids augment insulin secretion. J Am Coll Nutr. 1987 Dec;6(6):507–515. doi: 10.1080/07315724.1987.10720210. [DOI] [PubMed] [Google Scholar]
- Lardinois C. K. The role of omega 3 fatty acids on insulin secretion and insulin sensitivity. Med Hypotheses. 1987 Nov;24(3):243–248. doi: 10.1016/0306-9877(87)90071-5. [DOI] [PubMed] [Google Scholar]
- Lopes-Virella M. F., Stone P., Ellis S., Colwell J. A. Cholesterol determination in high-density lipoproteins separated by three different methods. Clin Chem. 1977 May;23(5):882–884. [PubMed] [Google Scholar]
- McMichael A. J., Jensen O. M., Parkin D. M., Zaridze D. G. Dietary and endogenous cholesterol and human cancer. Epidemiol Rev. 1984;6:192–216. doi: 10.1093/oxfordjournals.epirev.a036271. [DOI] [PubMed] [Google Scholar]
- Moley J. F., Morrison S. D., Gorschboth C. M., Norton J. A. Body composition changes in rats with experimental cancer cachexia: improvement with exogenous insulin. Cancer Res. 1988 May 15;48(10):2784–2787. [PubMed] [Google Scholar]
- Mountjoy K. G., Finlay G. J., Holdaway I. M. Abnormal insulin-receptor down regulation and dissociation of down regulation from insulin biological action in cultured human tumor cells. Cancer Res. 1987 Dec 15;47(24 Pt 1):6500–6504. [PubMed] [Google Scholar]
- Mountjoy K. G., Holdaway I. M., Finlay G. J. Insulin receptor regulation in cultured human tumor cells. Cancer Res. 1983 Oct;43(10):4537–4542. [PubMed] [Google Scholar]
- Nathanson L., Hall T. C. A spectrum of tumors that produce paraneoplastic syndromes. Lung tumors: how they produce their syndromes. Ann N Y Acad Sci. 1974;230:367–377. doi: 10.1111/j.1749-6632.1974.tb14471.x. [DOI] [PubMed] [Google Scholar]
- O'Connor T. P., Roebuck B. D., Peterson F., Campbell T. C. Effect of dietary intake of fish oil and fish protein on the development of L-azaserine-induced preneoplastic lesions in the rat pancreas. J Natl Cancer Inst. 1985 Nov;75(5):959–962. doi: 10.1093/jnci/75.5.959. [DOI] [PubMed] [Google Scholar]
- Pavelić K., Slijepcević M. Growth of a thymoma in diabetic mice treated with insulin. Eur J Cancer. 1978 Jun;14(6):675–679. doi: 10.1016/0014-2964(78)90303-1. [DOI] [PubMed] [Google Scholar]
- Pennock C. A., Murphy D., Sellers J., Longdon K. J. A comparison of autoanalyser methods for the estimation of glucose in blood. Clin Chim Acta. 1973 Oct 12;48(2):193–201. doi: 10.1016/0009-8981(73)90365-3. [DOI] [PubMed] [Google Scholar]
- Reddy B. S., Maruyama H. Effect of dietary fish oil on azoxymethane-induced colon carcinogenesis in male F344 rats. Cancer Res. 1986 Jul;46(7):3367–3370. [PubMed] [Google Scholar]
- Reddy B. S., Sugie S. Effect of different levels of omega-3 and omega-6 fatty acids on azoxymethane-induced colon carcinogenesis in F344 rats. Cancer Res. 1988 Dec 1;48(23):6642–6647. [PubMed] [Google Scholar]
- Roebuck B. D., Yager J. D., Jr, Longnecker D. S., Wilpone S. A. Promotion by unsaturated fat of azaserine-induced pancreatic carcinogenesis in the rat. Cancer Res. 1981 Oct;41(10):3961–3966. [PubMed] [Google Scholar]
- SALTER J. M., DE MEYER R., BEST C. H. Effect of insulin and glucagon on tumour growth. Br Med J. 1958 Jul 5;2(5087):5–7. doi: 10.1136/bmj.2.5087.5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Siedel J., Hägele E. O., Ziegenhorn J., Wahlefeld A. W. Reagent for the enzymatic determination of serum total cholesterol with improved lipolytic efficiency. Clin Chem. 1983 Jun;29(6):1075–1080. [PubMed] [Google Scholar]
- Yam D., Zilberstein A., Fink A., Nir I. Insulin-tumour interrelationship in EL4 lymphoma or thymoma-bearing mice. I. Alloxan-diabetic or non-diabetic mice. Br J Cancer. 1990 May;61(5):689–694. doi: 10.1038/bjc.1990.156. [DOI] [PMC free article] [PubMed] [Google Scholar]
- de Waard F. Breast cancer incidence and nutritional status with particular reference to body weight and height. Cancer Res. 1975 Nov;35(11 Pt 2):3351–3356. [PubMed] [Google Scholar]
