|
| This article is part of a series on Estrogen receptor transcription and transactivation, edited by Pierre Chambon.This article is part of the supplement: 23rd Congress of the International Association for Breast Cancer ResearchMeeting abstractEstrogen receptor transcription and transactivation: Novel morphoregulatory functions for the adhesion receptor Ep-CAM in the mammary epithelium1Department of Pathology and Division of Laboratory Animals, Leiden University Medical Center, Leiden, The Netherlands 2The Whittier Institute for Diabetes, University of California San Diego, La Jolla, California, USA from 23rd Congress of the International Association for Breast Cancer Research Breast Cancer Res 2001, 3(Suppl 1):A11doi:10.1186/bcr335
© 2001 BioMed Central Ltd Meeting abstractEp-CAM, an epithelial cell-cell adhesion receptor, is often over-expressed in association with proliferation and remodeling in epithelial tissues. Development of the mouse mammary gland during pregnancy is associated with a progressive upregulation of Ep-CAM expression, eventually reaching very high levels at day 16 of pregnancy. This phenomenon is paralleled by a concomitant branching of the mammary ductal tree and a sustained epithelial cell proliferation. Using a MMTV-LTR/Ep-CAM transgenic mouse model, we demonstrate that forced expression of Ep-CAM in the mammary epithelium leads to an induction of budding and secondary branching of the glandular tree in virgin females. Interestingly, a complete cycle of gestation in the Ep-CAM transgenic mice results in extreme ductal hyperplasia/ductectasia and lobular hypoplasia, in combination with partially decreased differentiation of both ductal and alveolar (lobular) epithelial cells. Surprisingly, mammary gland involution is affected because of a decreased frequency of apoptotic figures and increased rate of cell proliferation. These results support novel morphoregulatory functions for the adhesion receptor Ep-CAM in epithelial tissue development and homeostasis. Have something to say? Post a comment on this article! |



on Google Scholar




