<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>Piguet, Anne-Christine</dc:creator>
  <dc:creator>Saar, Bettina</dc:creator>
  <dc:creator>Hlushchuk, Ruslan</dc:creator>
  <dc:creator>St-Pierre, Marie V.</dc:creator>
  <dc:creator>McSheehy, Paul M.</dc:creator>
  <dc:creator>Radojevic, Vesna</dc:creator>
  <dc:creator>Afthinos, Maresa</dc:creator>
  <dc:creator>Terracciano, Luigi</dc:creator>
  <dc:creator>Djonov, Valentin</dc:creator>
  <dc:creator>Dufour, Jean-François</dc:creator>
  <dc:date>2011-04-12</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Sorafenib targets the Raf/mitogen activated protein kinase, VEGF and PDGF  pathways and prolongs survival patients in advanced hepatocellular carcinoma  (HCC). Everolimus inhibits the mammalian target of rapamycin, a kinase overactive in  HCC. To investigate whether the antitumor effects of these agents are additive, we  compared a combined and sequential treatment regimen of everolimus and sorafenib  with monotherapy. After hepatic implantation of Morris Hepatoma cells, rats were  randomly allocated to everolimus (5mg/kg, 2x/week), sorafenib (7.5mg/kg/day),  combined everolimus and sorafenib, sequential sorafenib (2 weeks) then everolimus  (3 weeks), or control groups. Magnetic resonance imaging quantified tumor volumes.  Erk1/2, 4E-BP1 and their phosphorylated forms were quantified by immunoblotting.  Angiogenesis was assessed in vitro by aortic ring and tube formation assays, and in  vivo with Vegf-a mRNA and vascular casts. After 35 days, tumor volumes were  reduced by 60%, 85% and 55%, relative to controls, in everolimus, the combination  and sequential groups, respectively (p&lt;0.01). Survival was longest in the combination  group (p&lt;0.001). Phosphorylation of 4E-BP1 and Erk1/2 decreased after everolimus  and sorafenib, respectively. Angiogenesis decreased after all treatments (p&lt;0.05),  although sorafenib increased Vegf-a mRNA in liver tumors. Vessel sprouting was  abundant in control tumors, lower after sorafenib and absent after the combination.  Intussusceptive angiogenic transluminal pillars failed to coalesce after the  combination. Combined treatment with everolimus and sorafenib exerts a stronger  antitumoral effect on MH tumors than monotherapy. Everolimus retains antitumoral  properties when administered sequentially after sorafenib. This supports the clinical  use of everolimus in HCC, both in combination with sorafenib or after sorafenib.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/301885</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/301885/files/djo_eae.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1158/1535-7163.MCT-10-0666</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Molecular Cancer Therapeutics. - 2011, vol. 10, no. 6, p. 1007-1017</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Everolimus augments the effects of sorafenib in a syngeneic orthotopic model of hepatocellular carcinoma</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
