<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>Estermann, Manuela</dc:creator>
  <dc:creator>Huang, Yen-Lin</dc:creator>
  <dc:creator>Septiadi, Dedy</dc:creator>
  <dc:creator>Ritz, Danilo</dc:creator>
  <dc:creator>Liang, Ching-Yeu</dc:creator>
  <dc:creator>Jacob, Francis</dc:creator>
  <dc:creator>Drasler, Barbara</dc:creator>
  <dc:creator>Petri-Fink, Alke</dc:creator>
  <dc:creator>Heinzelmann-Schwarz, Viola</dc:creator>
  <dc:creator>Rothen-Rutishauser, Barbara</dc:creator>
  <dc:date>2020-12-03</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">The presence of ascites in the peritoneal cavity leads to morphological and functional  changes of the peritoneal mesothelial cell layer. Cells loose cell-cell interactions,  rearrange their cytoskeleton, activate the production of fibronectin, and change their  cell surface morphology in a proinflammatory environment. Moreover, ovarian cancer  cell adhesion has been shown to be facilitated by these changes due to increased  integrin- and CD44-mediated binding sites. In this study, the biological responsiveness  of the human pleural mesothelial cell line MeT-5A to patient-derived and artificial  ascites was studied in vitro and adhesion of ovarian cancer cells, i.e. SKOV-3 cells,  investigated. Changes were mainly observed in cells exposed to artificial ascites  containing higher cytokine concentrations than patient-derived ascites. Interestingly,  reduced cell-cell interactions were already observed in untreated MeT-5A cells and  effects on tight junction protein expression and permeability upon exposure to ascites  were minor. Ascites induced upregulation of CDC42 effector protein 2 expression,  which affects stress fiber formation, however significant F-actin reorganization was not  observed. Moreover, fibronectin production remained unchanged. Analysis of  mesothelial cell surface characteristics showed upregulated expression of intercellular  adhesion molecule 1, slightly increased hyaluronic acid secretion and decreased  microvillus expression upon exposure to ascites. Nevertheless, the observed changes  were not sufficient to facilitate adhesion of SKOV-3 cells on MeT-5A cell layer. This  study revealed that MeT-5A cells show a reduced biological responsiveness to the  presence of ascites, in contrast to published studies on primary human peritoneal  mesothelial cells.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/309081</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/309081/files/fin_pda.pdf</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/309081/files/fin_pda_sm.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1371/journal.pone.0241500</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>PLOS ONE. - 2020, vol. 15, no. 12, p. e0241500</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Ascites</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Cytokines</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Ovarian cancer</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Cell adhesion</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Microvilli</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">Secretion</dc:subject>
  <dc:subject xmlns:ns7="xml" ns7:lang="en">Permeability</dc:subject>
  <dc:subject xmlns:ns8="xml" ns8:lang="en">Cytoskeleton</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns9="xml" ns9:lang="en">Patient-derived and artificial ascites have minor effects on MeT-5A mesothelial cells and do not facilitate ovarian cancer cell adhesion</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
