<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Brennecke, Patrick</dc:creator>
  <dc:creator>Arlt, Matthias J. E.</dc:creator>
  <dc:creator>Muff, Roman</dc:creator>
  <dc:creator>Campanile, Carmen</dc:creator>
  <dc:creator>Gvozdenovic, Ana</dc:creator>
  <dc:creator>Husmann, Knut</dc:creator>
  <dc:creator>Holzwarth, Nathalie</dc:creator>
  <dc:creator>Cameroni, Elisabetta</dc:creator>
  <dc:creator>Ehrensperger, Felix</dc:creator>
  <dc:creator>Thelen, Marcus</dc:creator>
  <dc:creator>Born, Walter</dc:creator>
  <dc:creator>Fuchs, Bruno</dc:creator>
  <dc:date>2013-09-10</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">More effective treatment of metastasizing osteosarcoma with a current mean 5-year survival  rate of less than 20% requires more detailed knowledge on mechanisms and key regulatory  molecules of the complex metastatic process. CXCR4, the receptor of the chemokine CXCL12,  has been reported to promote tumor progression and metastasis in osteosarcoma. CXCR7 is a  recently deorphanized CXCL12-scavenging receptor with so far not well-defined functions in  tumor biology. The present study focused on a potential malignancy enhancing function of  CXCR7 in interaction with CXCR4 in osteosarcoma, which was investigated in an intratibial  osteosarcoma model in SCID mice, making use of the human 143B osteosarcoma cell line that  spontaneously metastasizes to the lung and expresses endogenous CXCR4. 143B  osteosarcoma cells stably expressing LacZ (143B-LacZ cells) were retrovirally transduced with  a gene encoding HA-tagged CXCR7 (143B-LacZ-X7-HA cells). 143B-LacZ-X7-HA cells  coexpressing CXCR7 and CXCR4 exhibited CXCL12 scavenging and enhanced adhesion to  IL-1β-activated HUVEC cells compared to 143B-LacZ cells expressing CXCR4 alone. SCID  mice intratibially injected with 143B-LacZ-X7-HA cells had significantly (p&lt;0.05) smaller primary  tumors, but significantly (p&lt;0.05) higher numbers of lung metastases than mice injected with  143B-LacZ cells. Unexpectedly, 143B-LacZ-X7-HA cells, unlike 143B-LacZ cells, also  metastasized with high incidence to the auriculum cordis. In conclusion, expression of the  CXCL12 scavenging receptor CXCR7 in the CXCR4-expressing human 143B osteosarcoma  cell line enhances its metastatic activity in intratibial primary tumors in SCID mice that  predominantly metastasize to the lung and thereby closely mimic the human disease. These  findings point to CXCR7 as a target, complementary to previously proposed CXCR4, for more  effective metastasis-suppressive treatment in osteosarcoma.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://susi.usi.ch/global/documents/318911</dc:identifier>
  <dc:identifier>https://localhost:5000/ark:/12658/srd1318911</dc:identifier>
  <dc:identifier>https://susi.usi.ch/documents/318911/files/brennecke_pone_2013.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1371/journal.pone.0074045</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/ark/12658/srd1318911</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>CC BY</dc:rights>
  <dc:source>Plos one. - 2013, vol. 8, no. 9, p. e74045</dc:source>
  <dc:subject>info:eu-repo/classification/udc/61</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Expression of the chemokine receptor CXCR7 in CXCR4-expressing human 143B osteosarcoma cells enhances lung metastasis of intratibial xenografts in SCID mice</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
