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<H1 class=3Dpage-header>Short Communication</H1>
<P id=3Dcite><I>Oncogene</I> (2006) <B>25,</B> 2801=962806.=20
doi:10.1038/sj.onc.1209302; published online 9 January 2006</P>
<H2 id=3Datl>CXCR4 expression mediates glioma cell invasiveness</H2>
<P id=3Daug>M&nbsp;Ehtesham<SUP><A title=3D"affiliated with 1"=20
href=3D"http://www.nature.com/onc/journal/v25/n19/abs/1209302a.html;jsess=
ionid=3DB449B61B46A38B8E8973BB1C88AD233E#aff1">1</A>,<A=20
title=3D"affiliated with 2"=20
href=3D"http://www.nature.com/onc/journal/v25/n19/abs/1209302a.html;jsess=
ionid=3DB449B61B46A38B8E8973BB1C88AD233E#aff2">2</A>,<A=20
title=3D"affiliated with 3"=20
href=3D"http://www.nature.com/onc/journal/v25/n19/abs/1209302a.html;jsess=
ionid=3DB449B61B46A38B8E8973BB1C88AD233E#aff3">3</A></SUP>,=20
J A&nbsp;Winston<SUP><A title=3D"affiliated with 1"=20
href=3D"http://www.nature.com/onc/journal/v25/n19/abs/1209302a.html;jsess=
ionid=3DB449B61B46A38B8E8973BB1C88AD233E#aff1">1</A></SUP>,=20
P&nbsp;Kabos<SUP><A title=3D"affiliated with 4"=20
href=3D"http://www.nature.com/onc/journal/v25/n19/abs/1209302a.html;jsess=
ionid=3DB449B61B46A38B8E8973BB1C88AD233E#aff4">4</A></SUP>=20
and R C&nbsp;Thompson<SUP><A title=3D"affiliated with 1"=20
href=3D"http://www.nature.com/onc/journal/v25/n19/abs/1209302a.html;jsess=
ionid=3DB449B61B46A38B8E8973BB1C88AD233E#aff1">1</A>,<A=20
title=3D"affiliated with 3"=20
href=3D"http://www.nature.com/onc/journal/v25/n19/abs/1209302a.html;jsess=
ionid=3DB449B61B46A38B8E8973BB1C88AD233E#aff3">3</A></SUP></P>
<DIV id=3Daffiliations-notes>
<OL>
  <LI id=3Daff1><SUP>1</SUP>Department of Neurological Surgery, =
Vanderbilt=20
  University Medical Center, Nashville, TN, USA
  <LI id=3Daff2><SUP>2</SUP>Department of Cancer Biology, Vanderbilt =
University=20
  Medical Center, Nashville, TN, USA
  <LI id=3Daff3><SUP>3</SUP>Vanderbilt Ingram Cancer Center, Vanderbilt =
University=20
  Medical Center, Nashville, TN, USA
  <LI id=3Daff4><SUP>4</SUP>Department of Medicine, University of =
Southern=20
  California, Los Angeles, CA, USA</LI></OL>
<P class=3Dcaff>Correspondence: Dr M Ehtesham, T-4224, Medical Center =
North,=20
Vanderbilt University Medical Center, Nashville, TN 37232-2380, USA. =
E-mail: <A=20
href=3D"mailto:moneeb.ehtesham@vanderbilt.edu">moneeb.ehtesham@vanderbilt=
.edu</A></P>
<P class=3Dprdates>Received 18&nbsp;December&nbsp;2004; Revised=20
27&nbsp;October&nbsp;2005; Accepted 4&nbsp;November&nbsp;2005; Published =
online=20
9&nbsp;January&nbsp;2006. </P></DIV>
<DIV id=3Dabs><A class=3Dbacktotop=20
href=3D"http://www.nature.com/onc/journal/v25/n19/abs/1209302a.html;jsess=
ionid=3DB449B61B46A38B8E8973BB1C88AD233E#top">Top<SPAN=20
class=3Dhidden> of page</SPAN></A>
<H3>Abstract</H3>
<P class=3Dlead>Glioblastoma multiforme is a highly invasive tumor =
bearing a=20
dismal prognosis. Experimental strategies that focus on the specific =
biological=20
cues governing the invasive capacity of these tumors may hold =
significant=20
therapeutic promise. In this context, we describe the <I>in vitro</I> =
and <I>in=20
vivo</I> association of the cell surface chemokine receptor, CXCR4, with =
the=20
development of an invasive phenotype in malignant glioblastoma. We =
demonstrate=20
that invasive populations of glioma cells overexpress CXCR4 at the =
message and=20
protein levels, and that this expression ranges from 25- to 89-fold =
higher than=20
that found in noninvasive tumor cells. Furthermore, neutralization of =
CXCR4=20
significantly impairs the <I>in vitro</I> invasive capacity of malignant =
glial=20
cells. In addition, glioma cells secrete CXCL12 and demonstrate robust =
invasive=20
capacity toward a CXCL12 gradient <I>in vitro</I>. These findings =
underscore the=20
importance of CXCR4 as a potential therapeutic target for the treatment =
of=20
invasive glioblastoma.</P>
<DIV class=3Dkeyw-abbr>
<H4 class=3Dkeywords>Keywords: </H4>
<P class=3Dkeywords>chemokine, CXCR4, invasion, glioma, brain=20
tumor</P></DIV></DIV>
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}
 HTML DIV.ad-vert {
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}
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}
DIV.natjobmore {
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P.nateventmore {
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DIV.natprodmore INPUT {
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}
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}
DIV.natprodmore INPUT {
=09
}
DIV.natprodmore INPUT {
=09
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BORDER-TOP: #000 1px solid; PADDING-LEFT: 10px; BACKGROUND: #eaeaea; =
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}
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BORDER-LEFT-WIDTH: 0px; BACKGROUND: none transparent scroll repeat 0% =
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}
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25px; FONT-SIZE: 70%; BACKGROUND: =
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BORDER-LEFT: black 1px solid; PADDING-TOP: 0px
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}
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BORDER-TOP: #000 1px solid; PADDING-LEFT: 10px; BACKGROUND: #eaeaea; =
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BORDER-BOTTOM: #000 1px solid
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