<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>Augsburger, Fiona</dc:creator>
  <dc:creator>Randi, Elisa B.</dc:creator>
  <dc:creator>Jendly, Mathieu</dc:creator>
  <dc:creator>Ascencao, Kelly</dc:creator>
  <dc:creator>Nahzli Dilek</dc:creator>
  <dc:creator>Szabo, Csaba</dc:creator>
  <dc:date>2020-03-13</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">3-mercaptopyruvate sulfurtransferase (3-MST) has emerged as one of the  significant sources of biologically active sulfur species in various mammalian  cells. The current study was designed to investigate the functional role of 3- MST’s catalytic activity in the murine colon cancer cell line CT26. The novel  pharmacological 3-MST inhibitor HMPSNE was used to assess cancer cell  proliferation, migration and bioenergetics in vitro. Methods included  measurements of cell viability (MTT and LDH assays), cell proliferation and in  vitro wound healing (IncuCyte) and cellular bioenergetics (Seahorse  extracellular flux analysis). 3-MST expression was detected by Western blotting;  H2S production was measured by the fluorescent dye AzMC. The results show  that CT26 cells express 3-MST protein and mRNA, as well as several enzymes  involved in H2S degradation (TST, ETHE1). Pharmacological inhibition of 3- MST concentration-dependently suppressed H2S production and, at 100 and  300 µM, attenuated CT26 proliferation and migration. HMPSNE exerted a bell- shaped effect on several cellular bioenergetic parameters related to oxidative  phosphorylation, while other bioenergetic parameters were either unaffected or  inhibited at the highest concentration of the inhibitor tested (300 µM). In contrast  to 3-MST, the expression of CBS (another H2S producing enzyme which has  been previously implicated in the regulation of various biological parameters in  other tumor cells) was not detectable in CT26 cells and pharmacological  inhibition of CBS exerted no significant effects on CT26 proliferation or  bioenergetics. In summary, 3-MST catalytic activity significantly contributes to  the regulation of cellular proliferation, migration and bioenergetics in CT26  murine colon cancer cells. The current studies identify 3-MST as the principal  source of biologically active H2S in this cell line</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/308680</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/308680/files/sza_rtm.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.3390/biom10030447</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Biomolecules. - 2020, vol. 10, no. 3, p. 447</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Role of 3-mercaptopyruvate sulfurtransferase in the regulation of proliferation, migration, and bioenergetics in murine colon cancer cells</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
