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<art>
   <ui>bcr1557</ui>
   <ji>BCJ</ji>
   <fm>
      <dochead>Poster Presentation</dochead>
      <bibl>
         <title>
            <p>Phenotypic characterization of mouse mammary epithelial stem and progenitor cells</p>
         </title>
         <aug>
            <au id="A1">
               <snm>Stingl</snm>
               <fnm>J</fnm>
               <insr iid="I1"/>
               <insr iid="I2"/>
            </au>
            <au id="A2">
               <snm>Eaves</snm>
               <fnm>CJ</fnm>
               <insr iid="I2"/>
            </au>
            <au id="A3">
               <snm>Watson</snm>
               <fnm>CJ</fnm>
               <insr iid="I1"/>
            </au>
         </aug>
         <insg>
            <ins id="I1">
               <p>Department of Pathology, University of Cambridge, Cambridge, UK</p>
            </ins>
            <ins id="I2">
               <p>Terry Fox Laboratory, British Columbia Cancer Research Centre, Vancouver, Canada</p>
            </ins>
         </insg>
         <source>Breast Cancer Research</source>
         <supplement>
            <title>
               <p>Breast cancer research: the past and the future</p>
            </title>
            <note>Meeting abstracts</note>
         </supplement>
         <conference>
            <title>
               <p>Breast cancer research: the past and the future</p>
            </title>
            <location>London, UK</location>
            <date-range>1 November 2006</date-range>
            <url>http://www.breastcancercampaign.org</url>
         </conference>
         <issn>1465-5411</issn>
         <pubdate>2006</pubdate>
         <volume>8</volume>
         <issue>Suppl 2</issue>
         <fpage>P2</fpage>
         <xrefbib>
            <pubid idtype="doi">10.1186/bcr1557</pubid>
         </xrefbib>
      </bibl>
      <history>
         <pub>
            <date>
               <day>01</day>
               <month>11</month>
               <year>2006</year>
            </date>
         </pub>
      </history>
      <cpyrt>
         <year>2006</year>
         <collab>BioMed Central Ltd</collab>
      </cpyrt>
   </fm>
   <bdy>
      <sec>
         <st>
            <p/>
         </st>
         <p>Elucidation of the genes controlling the proliferation and differentiation of mouse mammary epithelial stem (MaSC) and progenitor (Ma-CFC) cells is paramount to understanding the processes that regulate mammary gland development and breast cancer progression. We have previously described a strategy in which MaSC and Ma-CFC can be purified to 5% and 15%, respectively, on the basis of lack of expression of the hematopoietic and endothelial markers CD45, Ter119 and CD31 and on the differential expression of CD24 and CD49f <abbrgrp><abbr bid="B1">1</abbr></abbrgrp>, with the MaSC having a CD24<sup>med</sup>CD49f<sup>high </sup>phenotype and the Ma-CFC having a CD24<sup>high</sup>CD49f<sup>low </sup>phenotype. Currently, a definitive analysis of the gene expression profiles of MaSC and Ma-CFC is not possible due to the presence of large numbers of contaminating cells in these enriched subpopulations. However, a preliminary microarray analysis of these subpopulations has identified potential new cell surface markers that can be exploited to further purify MaSC and Ma-CFC. We have initiated a screening program using the markers identified in the microarray analysis as well as markers used to identify other adult tissue stem cells to further purify and characterize MaSC and Ma-CFCs. Results of this screen will be presented.</p>
      </sec>
   </bdy>
   <bm>
      <ack>
         <sec>
            <st>
               <p>Acknowledgements</p>
            </st>
            <p>This work is supported by Breast Cancer Campaign.</p>
         </sec>
      </ack>
      <refgrp>
         <bibl id="B1">
            <title>
               <p>Purification and unique properties of mammary epithelial stem cells</p>
            </title>
            <aug>
               <au>
                  <snm>Stingl</snm>
                  <fnm>J</fnm>
               </au>
               <au>
                  <snm>Eirew</snm>
                  <fnm>P</fnm>
               </au>
               <au>
                  <snm>Ricketson</snm>
                  <fnm>I</fnm>
               </au>
               <au>
                  <snm>Shackletin</snm>
                  <fnm>M</fnm>
               </au>
               <au>
                  <snm>Vaillant</snm>
                  <fnm>F</fnm>
               </au>
               <au>
                  <snm>Choi</snm>
                  <fnm>D</fnm>
               </au>
               <au>
                  <snm>Li</snm>
                  <fnm>HI</fnm>
               </au>
               <au>
                  <snm>Eaves</snm>
                  <fnm>CJ</fnm>
               </au>
            </aug>
            <source>Nature</source>
            <pubdate>2006</pubdate>
            <volume>439</volume>
            <fpage>993</fpage>
            <lpage>997</lpage>
            <xrefbib>
               <pubid idtype="pmpid" link="fulltext">16395311</pubid>
            </xrefbib>
         </bibl>
      </refgrp>
   </bm>
</art>
