<?xml version='1.0'?>
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<art>
   <ui>bcr335</ui>
   <ji>BCJ</ji>
   <fm>
      <dochead>Meeting abstract</dochead>
      <bibl>
         <title>
            <p>Estrogen receptor transcription and transactivation: Novel morphoregulatory functions for the adhesion receptor Ep-CAM in the mammary epithelium</p>
         </title>
         <aug>
            <au id="A1">
               <snm>Blazar</snm>
               <fnm>M</fnm>
               <insr iid="I1"/>
            </au>
            <au id="A2">
               <snm>Cirulli</snm>
               <fnm>V</fnm>
               <insr iid="I2"/>
            </au>
            <au id="A3">
               <snm>Prins</snm>
               <fnm>F</fnm>
               <insr iid="I1"/>
            </au>
            <au id="A4">
               <snm>Litvinov</snm>
               <fnm>SV</fnm>
               <insr iid="I1"/>
            </au>
         </aug>
         <insg>
            <ins id="I1">
               <p>Department of Pathology and Division of Laboratory Animals, Leiden University Medical Center, Leiden, The Netherlands</p>
            </ins>
            <ins id="I2">
               <p>The Whittier Institute for Diabetes, University of California San Diego, La Jolla, California, USA</p>
            </ins>
         </insg>
         <source>Breast Cancer Res</source>
         <supplement>
            <title>
               <p>23rd Congress of the International Association for Breast Cancer Research</p>
            </title>
            <note>Meeting abstracts</note>
         </supplement>
         <conference>
            <title>
               <p>23rd Congress of the International Association for Breast Cancer Research</p>
            </title>
            <location>D&#252;sseldorf, Germany</location>
            <date-range>13&#8211;16 June 2001</date-range>
         </conference>
         <issn>1465-5411</issn>
         <pubdate>2001</pubdate>
         <volume>3</volume>
         <issue>Suppl 1</issue>
         <fpage>A11</fpage>
         <xrefbib>
            <pubid idtype="doi">10.1186/bcr335</pubid>
         </xrefbib>
      </bibl>
      <history>
         <rec>
            <date>
               <day>10</day>
               <month>5</month>
               <year>2001</year>
            </date>
         </rec>
         <pub>
            <date>
               <day>29</day>
               <month>5</month>
               <year>2001</year>
            </date>
         </pub>
      </history>
      <cpyrt>
         <year>2001</year>
         <collab>BioMed Central Ltd</collab>
      </cpyrt>
   </fm>
   <meta>
      <classifications>
         <classification type="BMC" subtype="old_arx_id">bcr-3-s1-a11</classification>
         <classification type="BMC" subtype="review_series_title" id="bcr_Estrogen">Estrogen receptor transcription and transactivation</classification>
         <classification type="BMC" subtype="review_series_editor" id="bcr_Estrogen">Pierre Chambon</classification>
      </classifications>
   </meta>
   <bdy>
      <sec>
         <st>
            <p/>
         </st>
         <p>Ep-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.</p>
      </sec>
   </bdy>
</art>
