Functional mammary gland development and oncogene-induced tumor formation are not affected by the absence of the retinoblastoma gene

G. W. Robinson, K. U. Wagner, L. Hennighausen

Research output: Contribution to journalArticle

30 Scopus citations

Abstract

Loss of cell cycle regulation in mammary epithelium results in impaired mammary gland development and neoplasia. We investigated the consequences of the absence of pRb in mammary epithelial cells during normal development and in mice that express an oncogene in the mammary epithelium. Since pRb-deficiency results in embryonic lethality, we transplanted pRb-null mammary anlagen into wild hosts, pRb-deficient mammary epithelia were capable of functional differentiation in term animals and they regenerated a differentiated gland even after multiple pregnancies. In serial transplantations no significant differences were found in outgrowth of pRb-deficient and wild type epithelia indicating that the absence of pRb does not lead to transformation. Likewise the effect of a TGFβ1 transgene was not altered in the absence of pRb. The susceptibility of mammary epithelium to form tumors was assessed in three different models. No differences in tumor incidence were found between wild type and Rb +/- WAP-int3, MMTV-PyMT transgenic and Brcal-/- epithelia. These results demonstrate that the absence of pRb does not affect normal mammary gland development and tumorigenesis in three different mouse models investigated and suggest that loss of more than one member of the pRb pathway is required to induce mammary tumors.

Original languageEnglish (US)
Pages (from-to)7115-7119
Number of pages5
JournalOncogene
Volume20
Issue number48
DOIs
StatePublished - Jan 1 2001

Keywords

  • Breast cancer
  • Mammary gland
  • Oncogenes
  • Pocket proteins
  • Tumor suppressor gene

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Cancer Research

Fingerprint Dive into the research topics of 'Functional mammary gland development and oncogene-induced tumor formation are not affected by the absence of the retinoblastoma gene'. Together they form a unique fingerprint.

  • Cite this