Skip to main content
Log in

Progesterone induction of mammary carcinomas in BALB/c female mice

Correlation between progestin dependence and morphology

  • Report
  • Published:
Breast Cancer Research and Treatment Aims and scope Submit manuscript

Summary

We have demonstrated that medroxyprogesterone acetate (MPA), when administered in high doses, induces mammary carcinomas in virgin female BALB/c mice. Since one of the possible explanations for this effect was its progestagenic effects, we decided to investigate whether progesterone (Pg) alone could also induce mammary adenocarcinomas in our model and if MPA at doses lower than those used to establish the model was also carcinogenic. A total of 136 mice were subdivided into 3 groups: Group 1, 44 mice were implanted s.c. with 40 mg Pg silastic pellets at the beginning of the experiment, and 6 months later with a 20 mg Pg pellet; Group 2, 45 mice were similarly treated with MPA pellets; Group 3, 47 mice were inoculated s.c. with 40 mg MPA every three months. At the end of 20 months, 9 animals had developed mammary tumors in Group 1, 18 in Group 2 and 34 in Group 3 (actuarial incidence = 28%, 58%, and 98%, respectively); tumor latency was similar in all groups: 46.2 ± 13.1, 51.3 ± 9.9, and 50.1 ± 2.1 weeks, respectively. Seven (Group 1), 14 (Group 2), and 25 (Group 3) tumors were transplanted into syngeneic mice to determine progestin dependence. All tumors, except one from Group 1, were histologically characterized. In Group 1 (Pg 60 mg), 4 tumors (67%) were infiltrating lobular carcinomas and 2 were ductal carcinomas (33%). In Group 2 (MPA 60 mg), 2 tumors (14%) were lobular and 12 were ductal adenocarcinomas (86%) (Group 1 vs Group 2: p < 0.05), whereas in Group 3 (MPA 160 mg), 8 were lobular carcinomas (32%) and 17 were ductal carcinomas (68%). In syngeneic passages all lobular tumors behaved as progestin independent (PI) and ductal tumors as progestin dependent (PD). All ductal tumors, except one, expressed estrogen receptors (ER) and progesterone receptors (PR), whereas receptor expression was variable in lobular carcinomas. It can be concluded that Pg induces mostly lobular, PI mammary tumors in BALB/c female mice. The fact that most MPA-induced tumors are ductal and PD suggests that the two hormones use different carcinogenic pathways.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

References

  1. Li J, Mueller G, Sekeley LI: Current perspectives and future trends in hormonal carcinogenesis. (Meeting report from the Division of Cancer Etiology, NCI, NIH.) Cancer Res 51: 3626–3629, 1991

    Google Scholar 

  2. Concannon P, Altszuler N, Hampshire J, Butler WR, Hansel W: Growth hormone, prolactin and cortisol in dogs developing mammary nodules and acromegaly-like appearance during treatment with medroxyprogesterone acetate. Endocrinology 106: 1173–1177, 1980

    Google Scholar 

  3. Nagasawa H, Aoki M, Sakagami N, Ishida M: Medroxyprogesterone acetate enhances spontaneous mammary tumorigenesis and uterine adenomyosis in mice. Breast Cancer Res Treat 12: 59–66, 1988

    Google Scholar 

  4. Russo IH, Gimotty P, Dupuis M, Russo J: Effect of medroxyprogesterone acetate on the response of the rat mammary gland to carcinogenesis. Br J Cancer 59: 210–216, 1989

    Google Scholar 

  5. Molinolo AA, Lanari C, Charreau EH, Sanjuan N, Dosne Pasqualini C: Mouse mammary tumors induced by medroxyprogesterone acetate: immunohistochemistry and hormonal receptors. J Natl Cancer Inst 79: 1341–1350, 1987

    Google Scholar 

  6. Pazos P, Lanari C, Meiss R, Charreau EH, Dosne Pasqualini C. Mammary carcinogenesis induced by N-methyl-N-nitrosourea (MNU) and medroxyprogesterone acetate (MPA) in BALB/c mice. Breast Cancer Res Treat 20: 133–138, 1992

    Google Scholar 

  7. Lanari C, Molinolo AA, Dosne Pasqualini C: Induction of mammary adenocarcinomas by medroxyprogesterone acetate in BALB/c female mice. Cancer Lett 33: 215–223, 1986

    Google Scholar 

  8. Lanari C, Kordon E, Molinolo AA, Dosne Pasqualini C, Charreau EH: Mammary adenocarcinomas induced by medroxyprogesterone acetate: hormone dependence and EGF receptors of BALB/cin vivo sublines. Int J Cancer 43: 845–850, 1989

    Google Scholar 

  9. Kiss R, Paridaens RJ, Heuson JC, Danguy AJ: Effect of progesterone on cell proliferation in the MXT mouse hormonesensitive mammary neoplasms. JNCI 77: 173–178, 1986

    Google Scholar 

  10. Nagasawa H, Yanai R, Nakajima Y, Mori J. Effects of progesterone on normal and preneoplastic development in mice in relation to prolactin and estrogen. Europ J Cancer 16: 1069–1077, 1980

    Google Scholar 

  11. Imagawa W, Tomooka Y, Hamamoto S, Nandi S: Stimulation of mammary epithelial cell growthin vitro. Interaction of epidermal growth factor and mammogenic hormones. Endocrinology 116: 1514–1524, 1985

    Google Scholar 

  12. Manni A, Badger B, Wright C, Ahmed SR, Demers LM: Effects of progestins on growth of experimental breast cancer in culture: Interaction with estradiol and prolactin and involvement of the polyamine pathway. Cancer Res 47: 3066–3071, 1987

    Google Scholar 

  13. Kordon E, Lanari C, Meiss R, Elizalde P, Charreau EH, Dosne Pasqualini C: Hormone-dependence of a mouse mammary tumor line induced by medroxyprogesterone acetate. Breast Cancer Res Treat 17: 33–43, 1990

    Google Scholar 

  14. Kordon E, Lanari C, Molinolo AA, Elizalde P, Charreau EH, Dosne Pasqualini C: Estrogen inhibition of MPA-induced mouse mammary tumor transplants. Int J Cancer 49: 900–905, 1991

    Google Scholar 

  15. Calandra RS, Charreau EH, Giaroli MR, Baldi A, Calvo JC, Pujato D, Arrighi L: Receptores para esteroides y prolactina en carcinomas mamarios humanos. Medicina (Bs Aires) 40: 718–725, 1980

    Google Scholar 

  16. Korenman SG, Dukes BA: Specific estrogen binding by the cytoplasm of human breast carcinoma. J Clin Endocrinol Metab 30: 639–654, 1970

    Google Scholar 

  17. Kaplan EL, Meier P: Non-parametric estimation for incomplete observation. J Am Stat Assoc 53: 457–481, 1958

    Google Scholar 

  18. Peto R, Pike MC, Armitage P, Breslow NE, Cox DR, Howard SW: Design and analysis of randomized clinical trials requiring prolonged observations of each patient. II. Analysis and examples. Br J Cancer 35: 1–19, 1977

    Google Scholar 

  19. Nandi S: Endocrine control of mammary gland development and function in the C3HHe Crgl mouse. J Natl Cancer Inst 21: 1039–1063, 1958

    Google Scholar 

  20. Freeman CS, Topper YJ: Progesterone is not essential to the differentiative potential of mammary epithelium in the male mouse. Endocrinology 103: 186–192, 1978

    Google Scholar 

  21. Haslam SZ: Role of sex steroid hormones in normal mammary gland function. In: Neville MC, Daniel CW (eds) The Mammary Gland: Development, Regulation and Function. Plenum Press, New York, 1987, pp 499–533

    Google Scholar 

  22. Masters JRW, Drife JO, Scarisbreck JJ: Cyclic variation of DNA synthesis in human breast epithelium. J Natl Cancer Inst 58: 1263–1265, 1977

    Google Scholar 

  23. Meyer JS: Cell proliferation in normal human breast ducts, fibroadenomas and other ductal hyperplasias measured by nuclear labeling with tritiated thymidine. Human Pathol 8: 67–81, 1977

    Google Scholar 

  24. Horwitz KB, Freidenberg GR: Growth inhibition and increase of insulin receptors in an anti-estrogen resistant T47Dco human breast cancer cells by progestins: Implications for endocrine therapies. Cancer Res 45: 167–173, 1985

    Google Scholar 

  25. Vonderhaar BK: Prolactin. Transport, function, and receptors in mammary gland development and differentiation. In: Neville MC, Daniel CW (eds) The Mammary Gland: Development, Regulation and Function. Plenum Press, New York, 1987, pp 383–438

    Google Scholar 

  26. Rosen JM, O'Neal DL, Mc Hugh JE, Comstock JP: Progesterone-mediated inhibition of casein mRNA and polysomal casein synthesis in the rat mammary gland during pregnancy. Biochemistry 17: 290–297, 1978

    Google Scholar 

  27. Farber E, Cameron R: Sequential analysis of cancer development. Adv Cancer Res 31: 125–226, 1980

    Google Scholar 

  28. Cato ACB, Skroch P, Butkeraitis P, Ponta H: The multi-hormonal regulation of transcription at the mouse mammary tumour virus promoter. In: Bresciani F, King RJB, Lippman ME, Raynaud JP (eds) Hormones and Cancer. Raven Press, New York, 1988, pp 114–117

    Google Scholar 

  29. Medina D: Preneoplastic lesions in murine mammary cancer. Cancer Res 36: 2589–2595, 1976

    Google Scholar 

  30. Michalides R, van Ooyen A, Nusse R: Mouse mammary tumor virus expression and mammary tumor development. Curr Top Microbiol Immunol 106: 57–78, 1983

    Google Scholar 

  31. Pollow K, Grill HJ, Heubner A, Manz B, Kreienberg R, Schmidt-Gollwitzer M: Medroxyprogesterone acetate therapy in endometrial carcinoma: mechanism of action, pharmacokinetics and clinical investigations. In: Bresciani F, King RJB, Lippman ME, Raynaud JP (eds) Hormones and Cancer. Raven Press, New York, 1988, pp 436–444

    Google Scholar 

  32. Liehr GJ: Genotoxic effects of estrogens. Mut Res 238: 269–276, 1990

    Google Scholar 

  33. Bullock LP, Barthe TH, Mawzowicz I, North A, Bardin CW: The effect of progestin on submaxillary gland epidermal growth factor: Demonstration of androgenic, synandrogenic and anti-androgenic actions. Endocrinology 97: 189–195, 1975

    Google Scholar 

  34. Briggs MH, Briggs M: Glucocorticoid properties of progestogens. Steroids 22: 555–559, 1973

    Google Scholar 

  35. Mauvais-Jarvais P: Progesterone and progestins: a general overview. In: Wayne Bardin C, Milgrom E, Mauvais Jarvais P (eds) Progesterone and Progestins. Raven Press, New York, 1983, pp 1–16

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Kordon, E.C., Molinolo, A.A., Pasqualini, C.D. et al. Progesterone induction of mammary carcinomas in BALB/c female mice. Breast Cancer Res Tr 28, 29–39 (1993). https://doi.org/10.1007/BF00666353

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00666353

Key words

Navigation