Effect of sialoadenectomy on medroxyprogesterone-acetate-induced mammary carcinogenesis in BALB/c mice. Correlation between histology and epidermal-growth-factor receptor content

Int J Cancer. 1994 Oct 15;59(2):196-203. doi: 10.1002/ijc.2910590210.

Abstract

To evaluate the possible involvement of the salivary glands in the modulation of medroxyprogesterone (MPA)-induced mammary tumorigenesis, 48 sialoadenectomized virgin BALB/c female mice and 47 controls were treated with 40mg MPA depot s.c. every 3 months for 1 year. Mammary tumors developed in 11 sialoadenectomized and in 34 control mice with similar latencies. In both groups, 75% of the tumors were ductal and progestin-dependent (PD) while the remainder were lobular and progestin-independent (PI). Epidermal growth factor (EGF) levels were measured in salivary glands (SG-EGF) and serum (S-EGF) in both groups. MPA induced a significant increase in SG-EGF and in S-EGF that became evident only after 1 month of MPA treatment. No increase in S-EGF was detected in MPA-treated sialoadenectomized mice, indicating that salivary glands are the major source of S-EGF. The presence of EGF receptors (EGF-R) was investigated in ductal PD and PI tumor lines and compared with 8 PI tumor lines of lobular origin. A significant difference in EGF-R content was found between lobular and ductal tumors. No increase in EGF-R was noted when ductal tumors became autonomous. EGF-R did not correlate with tumor growth rate and there was an inverse correlation between EGF-R and steroid receptors. When the effect of sialoadenectomy on tumor growth was tested in vivo in syngeneic transplants of 2 ductal PD, 1 ductal PI and 2 lobular PI mammary adenocarcinomas, it was not found to be significant when compared with the controls. It may be concluded that SG-EGF plays an important role in the induction of mammary adenocarcinomas by MPA, while it has no significant effect on the growth of established tumors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Division / physiology
  • Epidermal Growth Factor / blood
  • Epidermal Growth Factor / metabolism
  • Epidermal Growth Factor / physiology*
  • ErbB Receptors / analysis
  • ErbB Receptors / metabolism*
  • Female
  • Mammary Neoplasms, Experimental / chemically induced*
  • Mammary Neoplasms, Experimental / pathology*
  • Mammary Neoplasms, Experimental / ultrastructure
  • Medroxyprogesterone Acetate / toxicity*
  • Mice
  • Mice, Inbred BALB C
  • Neoplasms, Hormone-Dependent / chemically induced*
  • Neoplasms, Hormone-Dependent / pathology*
  • Neoplasms, Hormone-Dependent / ultrastructure
  • Salivary Glands / metabolism
  • Salivary Glands / physiology*
  • Salivary Glands / surgery

Substances

  • Epidermal Growth Factor
  • Medroxyprogesterone Acetate
  • ErbB Receptors