Skip to main content
Log in

Sex hormone-induced mammary carcinogenesis in female Noble rats: Expression of TGF-β1 and its receptors, TGF-α, and EGF-R in mammary carcinogenesis

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

Abstract

We have established a Noble rat model to explore the mechanisms of hormonal mammary carcinogenesis, in which the role of androgen in promoting mammary carcinogenesis was highlighted. We have also established that stromal–epithelial interactions may be responsible for the promotional effects of testosterone in mammary carcinogenesis. Based on these understandings, in the present study we examined the expression of transforming growth factor beta-1 (TGF-β1) and its receptors (TGF-β RI, TGF-β RII), transforming growth factor alpha (TGF-α), and epidermal growth factor receptor (EGF-R) in 'pre-malignant' mammary glands treated with different protocols of sex hormones, as well as in mammary cancers. We observed that TGF-β1 was strongly expressed in most mammary tumors, whereas TGF-β RI and TGF-β RII were negative in most mammary tumor cells. The results from comparative study of 'pre-malignant' glands further showed that when the animals were treated with testosterone, either alone or in combination with 17β-estradiol, the mammary gland epithelial cells expressed high levels of TGF-β1. This over-expression of TGF-β1 can be blocked by flutamide, indicating that testosterone may be responsible for the expression of TGF-β1 in mammary glands. TGF-β RI and TGF-β RII were also expressed strongly in testosterone-treated mammary epithelial cells and only weakly detectable in 17β-estradiol treated and control mammary epithelial cells. Furthermore, TGF-β RI and TGF-β RII were also expressed in stromal cells, both in mammary tumors and in hormone-treated mammary glands. These observations indicate that the mechanism of testosterone in mammary carcinogenesis may be through its regulation of expression of TGF-β1 and its receptors. On the other hand, TGF-α was also expressed in all 39 mammary cancers, while only 81% of the cancers were EGF-R positive. TGF-α was also strongly expressed in stromal cells in all three experimental groups, but only moderately expressed in epithelial cells when treated with a combination of testosterone and 17β-estradiol. By contrast, EGF-R was strongly expressed in epithelial cells in the three experimental groups but negative in stromal cells. Flutamide or tamoxifen was unable to block the expression of TGF-α induced by the combined sex hormone treatment. However, they were effective in blocking the expression of TGF-α when the animals were treated with testosterone or 17β-estradiol alone, respectively. These results suggest that both testosterone and 17β-estradiol may be required for the over-expression of TGF-α in the mammary carcinogenesis induced by sex hormones. To our knowledge, this is the first experimental study to explore the regulation of TGF-β1, TGF-α, and their receptors by testosterone and 17β-estradiol in mammary carcinogenesis.

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.

Similar content being viewed by others

References

  1. Parker SL, Tong T, Bolden S, Wingo PA: Cancer statistics 1997. CA Cancer J Clin 47: 5–27, 1997

    Article  PubMed  CAS  Google Scholar 

  2. Boyle, P. (1988) Epidemiology of breast cancer. Bailliere's Clin Oncol 2: 1.

    Google Scholar 

  3. Dickson RB, Lippman ME: Estrogenic regulation of growth and polypeptide growth factor secretion in human breast carcinoma. Endocr Rev 8: 29–43, 1987

    Article  PubMed  CAS  Google Scholar 

  4. Horwitz KB, McGuire WL: Nuclear mechanism of estrogen action. Effect of estradiol and anti-estrogens on estrogen receptors and nuclear receptor processing. J Biol Chem 253: 8185–8191, 1978

    PubMed  CAS  Google Scholar 

  5. Rochefort H, Garcia M: The estrogenic and antiestrogenic activites of androgens in female target tissues. Pharmacol Ther 23: 193–216, 1983

    Article  PubMed  CAS  Google Scholar 

  6. Kesey JL: Breast cancer epidemiology: Summary and future directions. Epidemiol Rev 15: 256–263, 1993

    Google Scholar 

  7. Berrino F, Muti P, Micheli A, Bolelli G, Krogh V, Sciajno R, Pisani P, Panico S, Secreto G: Serum sex hormone levels after menopause and subsequent breast cancer. J Natl Cancer Inst 88: 291–296, 1996

    Article  PubMed  CAS  Google Scholar 

  8. Bernstein L, Ross RK: Endogenous hormones and breast cancer risk. Epidemiol Rev 15: 48–65, 1993

    PubMed  CAS  Google Scholar 

  9. Sereto G, Toniolo P, Berrino F: Serum and urinary androgens and risk of breast cancer in postmenopausal women. Cancer Res 51: 2572–2576, 1991

    Google Scholar 

  10. Veronesi U, Pizzocaro G: Breast cancer in women subsequent to cystic disease of the breast. Surg Gynec Obst 126: 529–532, 1968

    CAS  Google Scholar 

  11. Secreto G, Toniolo P, Berrino F, Recchione C, Pietro SD, Fariselli G, Decarli A: Increased androgen activity and breast cancer risk in premenopausal women. Cancer Res 44: 5902–5905, 1984

    PubMed  CAS  Google Scholar 

  12. Dorgan JF, Longcope C, Stephenson Jr HE, Falk RT, Miller R, Franz C, Kahle L, Campbell WS, Tangrea JA, Schatzkin A: Serum sex hormone levels are related to breast cancer risk in postmenopausal women. Environ Health Perspect 105(Suppl.): 583–585, 1997

    PubMed  Google Scholar 

  13. Ruizeveld de Winter JA, Trapman J, Vermey M, Mulder E, Zegers ND, van der Kwast TH: Androgen receptor expression in human tissues: An immunohistochemical study. J Histochem Cytochem 39: 927, 1991

    Article  PubMed  CAS  Google Scholar 

  14. Janssen PJ, Brinkmann AO, Boersma WJ, van der Kwast TH: Immunohistochemical detection of the androgen receptor with monoclonal antibody F39.4 in routinely processed, paraffin238 embedded human tissues after microwave pre-treatment. J Histochem Cytochem 42: 1169–1175, 1994

    Article  PubMed  CAS  Google Scholar 

  15. Kimura N, Mizokami A: Immunocytochemical localization of androgen receptor with polyclonal antibody in paraffinembedded human tissues. J Histochem Cytochem 42: 126, 1994

    CAS  Google Scholar 

  16. Wong YC, Xie B, Tsao GSW: Induction of breast cancer in Noble rats with a combination of estrogen and testosterone. In: Li JJ, Daling J, Li SA (eds) Hormonal Carcinogenesis (Vol 3), Springer-Verlag (in press), 1999

  17. Xie B, Tsao SW, Wong YC: Induction of high incidence of mammary tumor in female Noble Rats with a combination of 17b-oestradiol and testosterone. Carcinogenesis 20: 1069–1078, 1999

    Article  PubMed  CAS  Google Scholar 

  18. Liao DJ, Hou X, Pantazis C, Bai S, Li SA, Li JJ: Combined treatment of estrogen and androgen is more effective than estrogen alone in induction of mammary adenocarcinoma in the male Noble rat ('abstract'). Am Asso Cancer Res 39: 387, 1998

    Google Scholar 

  19. Liao DJ, Pantazis CG, Hou X, Li SA: Promotion of estrogeninduced mammary gland carcinogenesis by androgen in the male Noble rat: Probable mediation by steroid receptor. Carcinogenesis 19: 2173–2180, 1998

    Article  PubMed  CAS  Google Scholar 

  20. Wakefield LM, Smith DM, Masui T, Harris CC, Sporn MB: Distribution and modulation of the cellular receptor for transforming growth factor b. J Cell Biol 105: 965–975, 1987

    Article  PubMed  CAS  Google Scholar 

  21. Gregoire M, Lieubeau B: The role of fibroblasts in tumor behavior. Cancer Metast Rev 14: 339–350, 1995

    Article  CAS  Google Scholar 

  22. Manning AM, Williams AC, Game SM, Paraskeva C: Differential sensitivity of human colonic adenoma and conversion of andenoma cell line to a tumorigenic phenotype is accompanied by a reduced response to the inhibitory effects of TGFb. Oncogene 6: 1471–1476, 1991

    PubMed  CAS  Google Scholar 

  23. Brattain MG, Markowitz SD, Willson JKV: The type II transforming growth factor-b receptor as a tumor-suppressor gene. Current Opinion in Oncology 8: 49–53, 1996

    Article  PubMed  CAS  Google Scholar 

  24. Vincent F, Hagiwara K, Ke Y, Stoner GD, Demetrick DJ, Bennett WP: Mutation analysis of transforming growth factor b type II receptor in sporadic human cancers of the pancreas, liver, and breast. Biochem Biophy Res Commun 223: 561–564, 1996

    Article  CAS  Google Scholar 

  25. Jakowlew SB, Moody TW, Mariano JM: Transforming growth factor-beta receptors in human cancer cell lines: Analysis of transcript, protein and proliferation. Anticancer Res 17: 1849–1860, 1997

    PubMed  CAS  Google Scholar 

  26. Rudland PS, Fernig DG, Smith JA: Growth factors and their receptors in neoplastic mammary glands. Biomed Pharmacother 49: 389–399, 1995

    Article  PubMed  CAS  Google Scholar 

  27. Panico L, D'Antonio A, Salvatore G, Mezza E, Tortora G, De Laurentiis M, De Placido S, Giordano T, Meino M, Salomon DS, Gullick WJ, Pettinato G, Schnitt SJ, Bianco AR, Ciardiello F: Differential immunohistochemical detection of transforming growth factor ?, amphiregulin and cripto in human normal and malignant breast tissues. Int J Cancer 65: 51–56, 1996

    Article  PubMed  CAS  Google Scholar 

  28. Bates SE, Davidson N, Valverius EM, Freter C, Dickson RB, Tam J, Kudlow J, Lippman ME, Salomon DS: Expression of transforming growth factor a and its messenger ribonucleic acid in human breast cancer: its regulation by estrogen and its possible functional significance. Mol Endocrinol 2: 543–555, 1988

    Article  PubMed  CAS  Google Scholar 

  29. Auvinen PK, Lipponen PK, Kataja VV, Johansson RT, Syrjanen KJ: Prognostic significance of TGF-alpha expression in breast cancer. Acta Oncol 35: 995–998, 1996

    Article  PubMed  CAS  Google Scholar 

  30. Levenson AS, Tonetti DA, Jordan VC: The oestrogen-like effect of 4-hydroxytamoxifen on induction of transforming growth factor alpha mRNA in MDA-MB-231 breast cancer cells stably expressing the oestrogen receptor. Br J Cancer 77: 1812–1819, 1998

    Article  PubMed  CAS  Google Scholar 

  31. Klijin JG, Berns PM, Schmitz PI, Foekens JA: The clinical significance of epidermal growth factor receptor (EGF-R) in human breast cancer: A review on 5232 patients. Endocr Rev 13: 3–9, 1992

    Google Scholar 

  32. Sneder SM, Diaugustine RP: Hormonal and environmental factors affecting cell proliferation and neoplasia in the mammary gland. Prog Clin Biol Res 394: 211–253, 1996

    Google Scholar 

  33. Lee CSL, Koga M, Sutherland RL: Modulation of estrogenreceptor and epidermal growth factor receptor messenger-RNAs by phorbol ester in MCF-7 breast cancer cells. Biochem Biophys Res Commun 162: 415–426, 1989

    Article  PubMed  CAS  Google Scholar 

  34. Bucci B, D'Agnano I, Botti C, Mottolese M, Carico E, Zupi G, Vecchione A: EGF-R expression in ductal breast cancer: Proliferation and prognostic implications. Anticancer Res 17: 769–774, 1997

    PubMed  CAS  Google Scholar 

  35. Rosen PP: Rosen's breast pathology. Lippincott-Raven, New York, 1997

    Google Scholar 

  36. Roberts AB, Thompson NL, Heine U, Flanders C, Sporn MB: Transforming growth factor-b: Possible roles in carcinogenesis. Br J Cancer 57: 594–600, 1988

    Article  PubMed  CAS  Google Scholar 

  37. Roberts AB, Sporn MB: Transforming growth factor b. Adv Cancer Res 51: 107–145, 1988

    Article  PubMed  CAS  Google Scholar 

  38. Zajchowoski D, Band V, Pauzid N, Iager A, Stampfer M, Sager R: Expression of growth factors and oncogenes in normal and tumor-derived human mammary epithelial cells. Cancer Res 48: 7041–7047, 1988

    Google Scholar 

  39. Valverius EM, Walker-Jones D, Bates SE, Stampfer MR, Mccormick F, Dickson RB, Lippman ME: Production of and responsiveness to transforming growth factor-beta in normal and oncogene-transformed human mammary epithelial cells. Cancer Res 49: 6269–6274, 1989

    PubMed  CAS  Google Scholar 

  40. Hong WK, Lippman ME, Itri LM, Karp DD, Leer JS, Byers RM, Schantz SP, Kramer AM, Lotan R, Peters LJ: Prevention of second primary tumors with isoretinoids in squamous cell carcinoma of the head and neck. N Engl J Med 323: 795–801, 1990

    Article  PubMed  CAS  Google Scholar 

  41. Airteaga CL, Dugger TC, Hurd SD: The multifunctional of transforming growth factor (TGF)-beta on mammary epithelial cell biology. Breast Cancer Res Treat 38: 49–56, 1996

    Article  Google Scholar 

  42. King RJ, Wang DY, Daly RJ, Darbre PD: Approaches to studying the role of growth factors in progression of breast tumors from the steroid sensitive to insensitive state. J Steroid Biochem, 34: 133–138, 1989

    Article  PubMed  CAS  Google Scholar 

  43. Daly RJ, King RJB, Darbre PD: Interaction of growth factors during the progression towards steroid independence in T-47-D human breast cancer cells. J Cell Biochem 43: 199–211, 1990

    Article  PubMed  CAS  Google Scholar 

  44. Welch DR, Fabra A, Nakajima M: Transforming growth factor beta stimulates mammary adenocarcinoma cell invasion and metastatic potential. Proc Natl Acad Sci USA 87: 7678–7682, 1990

    Article  PubMed  CAS  Google Scholar 

  45. Norgaard F, Hougaard S, Poulsen HS, Spang-Thomsen M: Transforming growth factor b and cancer. Cancer Treat Rev 21: 367–403, 1995

    Article  PubMed  CAS  Google Scholar 

  46. Azuma M, Yuki T, Tamatani T, Motegi K, Yoshida H, Sato M: Lake of expression of 44 transforming growth factor-b type II receptor associated with malignant progression in human salivary gland cell clones. Int J Cancer 66: 802–805, 1996

    Article  PubMed  CAS  Google Scholar 

  47. Myeroff LL, Parsons R, Kim SJ, Hedrick L, Cho KR, Orth K, Mathis M, Kinzler KW, Lutterbaugh J, Park K, Bang YJ, Lee HY, Park I-G, Lynch HT, Roberts AB, Vogelstein B, Markowitz SD: A transforming growth factor b receptor type II gene mutation common in colon and gastric but rare in endometrial cancers with microsatellite instablity. Cancer Res 55: 5545–5547, 1995

    PubMed  CAS  Google Scholar 

  48. Munoz-Antonia T, Li X, Reiss M, Jackson R, Antonia SA: Mutation in the transforming growth factor b type II receptor gene promoter associated with loss of gene expression. Cancer Res 56: 4831–4835, 1996

    PubMed  CAS  Google Scholar 

  49. Derynck R, Zhang Y: Intracellular signaling: the Mad way to do it. Curr Biol 6: 1226–1229, 1996

    Article  PubMed  CAS  Google Scholar 

  50. Macias-Silva M, Abdollah S, Hoodless PA, Pirone R, Attisano L, Wrana IL:MADR2 is a substrate of the TGF-b receptor and its phosphorylation is required for nuclear accumulation and signaling. Cell 87: 1215–1224, 1996

    Article  PubMed  CAS  Google Scholar 

  51. Chen Y, Lebrun JJ, Vale W: Regulation of transforming growth factor b and activin induced transcription by mammalian Mad protein. Proc Natl Acad Sci USA 93: 12992–12997, 1996

    Article  PubMed  CAS  Google Scholar 

  52. Lagna G, Hata A, Hemmati-Brivanlou A, Massague J: Partnership between DPC4 and SMAD proteins in TGF-b signaling pathways. Nature 383: 832–836, 1996

    Article  PubMed  CAS  Google Scholar 

  53. DeWinter JP, Roelen BA, ten Dijke P, van der Burg B, van den Eijnden-van Raaij AJ: DPC4 (SMAD4) mediates transforming growth factor-b1 (TGF-b1) induced growth inhibition and transcriptional response in breast tumor cells. Oncogene 14: 1891–1899, 1997

    Article  CAS  Google Scholar 

  54. Chen X, Weisberg E, Fridmacher V, Watanabe M, Naco G, Whitman M: Smad4 and FAST-1 in the assembly of activinresponsive factor. Nature 389: 85–89, 1997

    Article  PubMed  CAS  Google Scholar 

  55. Garrigue-Antar L, Munzo-Antonia T, Antonia SJ, Gesmonde J, Vellucci VF, Reiss M: Missense mutations of the transforming growth factor b type II receptor in human head and neck squamous carcinoma cells. Cancer Res 55: 3982–3987, 1995

    PubMed  CAS  Google Scholar 

  56. Takenoshita S, Tani M, Nagashima M, Hagiwara K, Bennett WP, Yokota J, Harris CC: Mutation analysis of coding sequences of the entire transforming growth factor b type II receptor gene in sporadic human colon cancer using genomic DNA and intron primers. Oncogene 14: 1255–1258, 1997

    Article  PubMed  CAS  Google Scholar 

  57. Langdon SP, Miller WR: Introduction to the cell and molecular biology of cancer. In: Langdon SF, Miller WR, Berchuck A (eds) Biology of female cancers. CRC press New York, 1997, pp 3–28

    Google Scholar 

  58. DiGiovanni J: Multistage carcinogenesis in mouse skin. Pharmac Ther 54: 63–128, 1992

    Article  CAS  Google Scholar 

  59. Wakefield LM, Letterio JJ, Geiser AG, Flander KC, O'shaugnessy J, Roberts AB, Sporn MB: Transforming growth factor-bs in mammary tumorigenesis: Promoters or antipromoters? In: McClain RM, Slaga TJ, LeBoeuf R, Pitot H (eds) Growth factors and tumor promotion. Wiley-Liss Press, New York, 1995, pp 133–148

    Google Scholar 

  60. Artagaveytia N, Le-Penven S, Falette N, Lucero R, Garofalo EG, Saez S: Epidermal growth factor and transforming growth factor alpha mRNA expression in human breast cancer biopsies; analysis in relation to estradiol, progesterone and EGF receptor content. J Steroid Biochem Mol Biol 60: 221–228, 1997

    Article  PubMed  CAS  Google Scholar 

  61. Schroeder W, Biesterfeld S, Zillessen S, Rath W: Epidermal growth factor receptor-immunohistochemical detection and clinical significance for treatment of primary breast cancer. Anticancer Res 17: 2799–2802, 1997

    PubMed  CAS  Google Scholar 

  62. Lee CS, deFazio A, Ormandy CJ, Sutherland RL: Inverse regulation of oestrogen receptor and epidermal growth factor receptor gene expression in MCF-7 breast cancer cells treated with phorbol ester. J Steroid Biochem Mol Biol 58: 267–275, 1996

    Article  PubMed  CAS  Google Scholar 

  63. Xie B, Tsao SW, Wong YC: Sex hormone-induced mammary carcinogenesis in female Noble rats: the rate of androgens. Carcinogenesis 20: 1597–1606, 1999

    Article  PubMed  CAS  Google Scholar 

Download references

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Xie, B., Tsao, S. & Wong, Y. Sex hormone-induced mammary carcinogenesis in female Noble rats: Expression of TGF-β1 and its receptors, TGF-α, and EGF-R in mammary carcinogenesis. Breast Cancer Res Treat 58, 227–239 (1999). https://doi.org/10.1023/A:1006349532643

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1006349532643

Navigation