<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>Wörthmüller, Janine</dc:creator>
  <dc:creator>Salicio, Valérie</dc:creator>
  <dc:creator>Oberson, Anne</dc:creator>
  <dc:creator>Blum, Walter</dc:creator>
  <dc:creator>Schwaller, Beat</dc:creator>
  <dc:date>2019</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Malignant mesothelioma (MM) is an aggressive asbestos-linked neoplasm,  characterized by dysregulation of signaling pathways. Due to intrinsic or acquired  chemoresistance, MM treatment options remain limited. Calretinin is a Ca2+-binding  protein expressed during MM tumorigenesis that activates the FAK signaling pathway,  promoting invasion and epithelial-to-mesenchymal transition. Constitutive calretinin  downregulation decreases MM cells’ growth and survival, and impairs tumor formation  in vivo. In order to evaluate early molecular events occurring during calretinin  downregulation, we generated a tightly controlled IPTG-inducible expression system  to modulate calretinin levels in vitro. Calretinin downregulation significantly reduced  viability and proliferation of MM cells, attenuated FAK signaling and reduced the  invasive phenotype of surviving cells. Importantly, surviving cells showed a higher  resistance to cisplatin due to increased Wnt signaling. This resistance was abrogated  by the Wnt signaling pathway inhibitor 3289-8625. In various MM cell lines and  regardless of calretinin expression levels, blocking of FAK signaling activated the Wnt  signaling pathway and vice versa. Thus, blocking both pathways had the strongest  impact on MM cell proliferation and survival. Chemoresistance mechanisms in MM  cells have resulted in a failure of single-agent therapies. Targeting of multiple  components of key signaling pathways, including Wnt signaling, might be the future  method-of-choice to treat MM.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/308346</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/308346/files/sch_mce.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.3390/ijms20215391</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>International Journal of Molecular Sciences. - 2019, vol. 20, no. 21, p. 5391</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Modulation of calretinin expression in human mesothelioma cells reveals the implication of the fak and wnt signaling pathways in conferring chemoresistance towards cisplatin</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
