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<art>
   <ui>bcr409</ui>
   <ji>BCJ</ji>
   <fm>
      <dochead>Meeting abstract</dochead>
      <bibl>
         <title>
            <p>Mutation detection in familial and sporadic breast cancers by denaturing high-performance liquid chromatography (DHPLC)</p>
         </title>
         <aug>
            <au id="A1">
               <snm>Betz</snm>
               <fnm>B</fnm>
               <insr iid="I1"/>
            </au>
            <au id="A2">
               <snm>Larbig</snm>
               <fnm>D</fnm>
               <insr iid="I1"/>
            </au>
            <au id="A3">
               <snm>Goecke</snm>
               <fnm>TO</fnm>
               <insr iid="I1"/>
            </au>
            <au id="A4">
               <snm>Nestle-Kr&#228;mling</snm>
               <fnm>C</fnm>
               <insr iid="I1"/>
            </au>
            <au id="A5">
               <snm>Bender</snm>
               <fnm>HG</fnm>
               <insr iid="I1"/>
            </au>
            <au id="A6">
               <snm>Niederacher</snm>
               <fnm>D</fnm>
               <insr iid="I1"/>
            </au>
         </aug>
         <insg>
            <ins id="I1">
               <p>Department of Obstetrics &amp; Gynecology, Heinrich-Heine-University, D&#252;sseldorf, Germany</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>A9</fpage>
         <xrefbib>
            <pubid idtype="doi">10.1186/bcr409</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-a9</classification>
      </classifications>
   </meta>
   <bdy>
      <sec>
         <st>
            <p>Objective</p>
         </st>
         <p>Denaturing high-performance liquid chromatography (DHPLC) is a recently developed method for detection of mutation that is gaining importance as a screening method for analyzing familial breast cancers, as well as heterogeneous tumor material.</p>
      </sec>
      <sec>
         <st>
            <p>Method</p>
         </st>
         <p>DHPLC was established for mutation detection in <it>BRCA1/2</it> diagnostic, using more than 200 different positive controls. Up until now, 64 DNA samples from patients with familial background for breast cancer (BC) were analyzed by DHPLC for <it>BRCA1/2</it> mutations. An additional 136 sporadic BC were examined for p53 mutations, analyzing exons 5-8 by DHPLC. Positive results were confirmed by direct DNA sequencing.</p>
      </sec>
      <sec>
         <st>
            <p>Results</p>
         </st>
         <p>The analysis of 64 DNA samples from patients with familial background for BC revealed several mutations and unclassified variants (UVs). Twenty-three different p53 mutations could be detected in 138 sporadic BC. Dilution of mutant DNA by wild-type DNA revealed the high sensitivity of this method: 5% mutant DNA is sufficient to achieve a positive DHPLC result. However, confirming a positive DHPLC result by DNA sequencing is difficult in heterogeneous tumor material.</p>
      </sec>
      <sec>
         <st>
            <p>Conclusion</p>
         </st>
         <p>DHPLC is a reliable, high-throughput technique for detection of mutation in familial breast cancers, as well as in heterogeneous tumor material.</p>
      </sec>
   </bdy>
</art>
