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   <ui>gb-spotlight-20010911-01</ui>
   <ji>GBJ</ji>
   <fm>
      <dochead>Research news</dochead>
      <bibl>
         <title>
            <p>Metastatic medulloblastoma</p>
         </title>
         <aug>
            <au id="A1">
               <snm>Weitzman</snm>
               <mi>B</mi>
               <fnm>Jonathan</fnm>
               <email>jonathanweitzman@hotmail.com</email>
            </au>
         </aug>
         <source>Genome Biology</source>
         <issn>1465-6906</issn>
         <pubdate>2001</pubdate>
         <volume>2</volume>
         <fpage>spotlight-20010911-01</fpage>
         <xrefbib>
            <pubid idtype="doi">10.1186/gb-spotlight-20010911-01</pubid>
         </xrefbib>
      </bibl>
      <history>
         <pub>
            <date>
               <day>11</day>
               <month>09</month>
               <year>2001</year>
            </date>
         </pub>
      </history>
      <cpyrt>
         <year>2001</year>
         <collab>BioMed Central Ltd</collab>
      </cpyrt>
      <shortabs>
         <p>Expression profiling identifies a set of genes associated with metastatic medulloblastomas.</p>
      </shortabs>
   </fm>
   <meta>
      <classifications>
         <classification type="STATUS">Archive</classification>
      </classifications>
   </meta>
   <bdy>
      <sec>
         <st>
            <p/>
         </st>
         <p><abbr bid="B1">Medulloblastoma</abbr> is the most common malignant brain cancer in children. In the Advanced Online Publication of <abbr bid="B2"><it>Nature Genetics</it></abbr>, Tobey MacDonald and colleagues from the <abbr bid="B3">Children's National Medical Center</abbr>, Washington, DC, report the use of oligonucleotide expression profiling (Affymetrix G110 cancer arrays) to define a set of genes that are prognostic for medulloblastoma metastasis (DOI:10.1038/ng731). They analysed 23 primary medulloblastomas that were either metastatic (M+) or non-metastatic (M0) and identified 85 genes that served for class prediction (59 genes were upregulated in metastatic tumours and 26 were decreased). This gene set could assign blinded tumour samples with high accuracy, and the set includes genes for the platelet-derived growth factor receptor alpha (PDGFRA) and components of the Ras/MAP kinase signalling pathway. MacDonald <it>et al.</it> provide additional functional evidence that PDGF and MAP kinase signalling events are important for medulloblastoma cell migration <it>in vitro</it> and propose that specific inhibitors of these signalling pathways may have therapeutic benefits.</p>
      </sec>
   </bdy>
   <bm>
      <refgrp>
         <bibl id="B1">
            <note>Medulloblastoma.</note>
            <xrefbib>
               <pubid idtype="pmpid">10676748</pubid>
            </xrefbib>
         </bibl>
         <bibl id="B2">
            <url>http://genetics.nature.com</url>
            <note>
               <it>Nature Genetics </it>
            </note>
         </bibl>
         <bibl id="B3">
            <url>http://www.cnmcresearch.org/</url>
            <note>Children's Research Institute</note>
         </bibl>
      </refgrp>
   </bm>
</art>
