Abstract
A role for ovarian and pituitary hormones in human breast cancer development has been suggested by observations such as the protective effects of a late age of menarche, an early age of menopause and first pregnancy and bilateral oopherectomy before the age 401,2. Similarly, completion of pregnancy and lactation or ovariectomy prior to carcinogen administration protects against mammary carcinogenesis in the rat3,4. Administration of a mammary carcinogen shortly before pregnancy enhances mammary tumor formation during the period of pregnancy and lactation compared to age-matched virgin controls5,6. Furthermore, treatment of rats with tamoxifen7,8 or 2-bromo-α-ergocryptine8, suppressers of estrogen and prolactin secretion respectively, at the time of, or shortly after carcinogen exposure, significantly inhibits tumorigenesis.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
Similar content being viewed by others
References
J.L. Kelsely, M.D. Gammon, and E.M. John, Reproductive factors and breast cancer. Epidemiol. Rev. 15:36 (1993).
J.R. Harris, M.E. Lippman, U. Veronesi, and W. Willett, Breast cancer. N. Eng. J. Med. 327:319 (1993).
I.H. Russo, and J. Russo, Mammary gland neoplasia in long-term rodent studies. Environ. Heallth. Prespect. 104:938 (1996).
C.W. Welsch, Host factors affecting the growth of carcinogen-induced rat mammary carcinomas: A review and tribute to Charles Brenton Huggins. Cancer Res. 45:3415 (1985).
G.M. McCormick, and R.C. Moon, Effect of pregnancy and lactation on growth of mammary tumors induced by 7,12-dimethylbenz(a)anthracine(DMBA). Br. J.Cancer. 19:160 (1965).
S. Sakamoto, Y. Imamura, S. Sassa, and R. Okamoto, DMBA-induced mammary tumor and hormone environment in the rat during pregnancy, postpartum, and long term lactation. Toxicol. Lett. 4:237 (1979).
M.M. Gottardis, and V.C. Jordan, Antitumor actions of ketoxifene and tamoxifen in the N-nitrosomethyl-urea-induced rat mammary carcinoma model. Cancer Res. 47:4020 (1987).
C.W. Welsch, M. Goodrich-Smith, C.K. Brown, D. Mackie, and D. Johnson, 2-Bromo-α-ergocryptin (CB-154) and tamoxifen (ICI 46,474) induced supression of the genesis of mammary carcinomas in female rats treated with 7,12-dimethylbenzanthracene (DMBA): a comparison. Oncol. 39:88 (1982).
R.A. Karmali, S. Welt, H.T. Thaler, and F. Lefevre, Prostaglandins in breast cancer: relationship to disease stage and hormone status. Br. J. Cancer. 48:689 (1983).
W.C. Tan, O.S. Privett, and M.E. Goldyne, Studies of prostaglandins in rat mammary tumors induced by 7,12-di-methylbenz(a)anthracene. Cancer Res. 34:3229 (1974).
C.A. Carter, R.J. Milholland, W. Shea, and M.M. Ip, Effect of the prostaglandin synthase inhibitor indomethacin on 7,12-dimethylbenz(a)anthracene-induced mammary tumorigenesis in rats fed different levels of fat Cancer Res. 43:3559 (1983).
G.M. Kollmorgen, M.M. King, S.D. Kosanke, and C. Do, Influence of dietary fat and indomethacin on the growth of transplantable mammary tumors in rats. Cancer Res. 43:4714 (1983).
H. Abou-Issa, and J.P. Minton, Loss of prostaglandin E receptors during progression of rat mammary tumors from hormonal dependence to autonomy. J. Natl. Cancer Inst. 76:101 (1986).
P.S. Rudland, A.C.T. Davies, and S.W. Tsao, Rat mammary preadipocytes in culture produce a trophic agent for mammary epithelia-prostaglandin E2. J. Cell Physiol. 120:364 (1984).
M.K. Foecking, W.E. Kibbey, H. Abou-Issa, R.H. Matthews, and J.P. Minton, Hormone dependence of 7,12-di-methylbenz[a]anthracene-induced mammary tumor growth: correlation with prostaglandin E2 content. J. Natl. Cancer Inst. 69:443 (1982).
X-H. Liu, and D.P. Rose, Differential expression and regulation of cyclooxygenase-1 and-2 in two human breast cancer cell lines. Cancer Res. 56:5125 (1996).
L.A. Cohen. (1986) Dietary fat and mammary cancer, in: Diet, Nutrition, and Cancer: A Critical Evaluation. B.S. Reddy and L.A. Cohen, eds., CRC Press, Inc, Boca Raton, FL (1986).
U. Mohr, and J.P. Lewkowski, The effect of diet on tumor development in animals. Expl. Pathol. S12:5 (1989).
C.P.J. Caygill, A. Chartert, and M.J. Hill, Fat, fish, fish oil, and cancer. Br. J. Cancer. 74:159 (1996).
M. Craig-Schmidt, M.T. White, P. Teer, J. Johnson, and H.W. Lane, Menhaden, coconut, and corn oils and mammary tumor incidence in BALB/c virgin female mice treated with DMBA. Nutr. Cancer. 20:99 (1993).
D.C. Cunningham, L.Y. Harrison, and T.D. Shultz, Proliferative responses of normal human mammary and MCF-7 breast cancer cells to linoleic acid, conjugated linoleic acid and eicosanoid synthesis 32. inhibitors in culture. Anticancer Res. 17:197 (1997).
D.F. Horrobin, The role of essential fatty acids and prostaglandins in breast cancer, in: Diet, Nutrition, and Cancer: A Critical Evaluation. B.S. Reddy, and L.A. Cohen, eds. CRC Press, Inc, Boca Raton, FL (1986).
A.F. Badawi, A. E1-Sohemy, L.L. Stephen, A.K. Ghoshal, and M.C. Archer, The effect of dietary n-3 and n-6 polyunsaturated fatty acids on the expression of cyclooxygenase 1 and 2 and levels of p21ras in rat mammary glands. Carcinogenesis. in press (1998
A.F. Badawi and M.C. Archer, Effect of hormonal status on the expression of the cyclooxygenase 1 and 2 genes and prostaglandin synthesis in rat mammary glands. Proc. Am. Assoc. Cancer Res. 39:590 (1998).
C.W. Welsch, Interaction of estrogen and prolactin in spontaneous mammary turnorigenesis in mouse. J. Toxicol. Environ. Health. 1:161 (1976).
C.W. Welsch, J.W. Jenkins, and J. Meites, Increased incidence of mammary tumors in the female rat grafted with multiple pituitaries. Cancer Res. 30:1024 (1970).
J.M. Connolly, and D.P. Rose, Effects of fatty acids on invasion through reconstituted basement membrane (‘Matrigel’) by human breast cancer cell line. Cancer Lett. 75:137 (1993).
T.E. Eling, and J.F. Curtis, Xenobiotic metabolism by prostaglandin Hsynthase. Pharmac. Ther. 53:261 (1992).
M. Tsuji, and R.N. DuBois, Alteration in cellular adhesion and apoptosis in epithelial cells overexpressing prostaglandin endoperoxide synthase 2. Cell. 83:493 (1995).
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1999 Springer Science+Business Media New York
About this chapter
Cite this chapter
Badawi, A.F., El-Sohemy, A., Stephen, L.L., Ghoshal, A.K., Archer, M.C. (1999). Modulation of the Expression of the Cyclooxygenase 1 and 2 Genes in Rat Mammary Glands: Role of Hormonal Status and Dietary Fat. In: Honn, K.V., Marnett, L.J., Nigam, S., Dennis, E.A. (eds) Eicosanoids and Other Bioactive Lipids in Cancer, Inflammation, and Radiation Injury, 4. Advances in Experimental Medicine and Biology, vol 469. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-4793-8_18
Download citation
DOI: https://doi.org/10.1007/978-1-4615-4793-8_18
Publisher Name: Springer, Boston, MA
Print ISBN: 978-1-4613-7171-7
Online ISBN: 978-1-4615-4793-8
eBook Packages: Springer Book Archive