1 Ocak 2019 Dergi makalesi Açık Erişim

Abdik, Ezgi Avsar; Kaleagasioglu, Ferda; Abdik, Hueseyin; Sahin, Fikrettin; Berger, Martin R.

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  <identifier identifierType="URL">https://aperta.ulakbim.gov.tr/record/72845</identifier>
  <creators>
    <creator>
      <creatorName>Abdik, Ezgi Avsar</creatorName>
      <givenName>Ezgi Avsar</givenName>
      <familyName>Abdik</familyName>
      <affiliation>Yeditepe Univ, Fac Engn, Dept Genet &amp; Bioengn, 26 August Campus,Kayisdagi St 326A, TR-34755 Istanbul, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Kaleagasioglu, Ferda</creatorName>
      <givenName>Ferda</givenName>
      <familyName>Kaleagasioglu</familyName>
    </creator>
    <creator>
      <creatorName>Abdik, Hueseyin</creatorName>
      <givenName>Hueseyin</givenName>
      <familyName>Abdik</familyName>
      <affiliation>Yeditepe Univ, Fac Engn, Dept Genet &amp; Bioengn, 26 August Campus,Kayisdagi St 326A, TR-34755 Istanbul, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Sahin, Fikrettin</creatorName>
      <givenName>Fikrettin</givenName>
      <familyName>Sahin</familyName>
      <affiliation>Yeditepe Univ, Fac Engn, Dept Genet &amp; Bioengn, 26 August Campus,Kayisdagi St 326A, TR-34755 Istanbul, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Berger, Martin R.</creatorName>
      <givenName>Martin R.</givenName>
      <familyName>Berger</familyName>
      <affiliation>German Canc Res Ctr, Toxicol &amp; Chemotherapy Unit, Heidelberg, Germany</affiliation>
    </creator>
  </creators>
  <titles>
    <title>Abt-737 And Erufosine Combination Against Castration-Resistant Prostate Cancer: A Promising But Cell-Type Specific Response Associated With The Modulation Of Anti-Apoptotic Signaling</title>
  </titles>
  <publisher>Aperta</publisher>
  <publicationYear>2019</publicationYear>
  <dates>
    <date dateType="Issued">2019-01-01</date>
  </dates>
  <resourceType resourceTypeGeneral="Text">Journal article</resourceType>
  <alternateIdentifiers>
    <alternateIdentifier alternateIdentifierType="url">https://aperta.ulakbim.gov.tr/record/72845</alternateIdentifier>
  </alternateIdentifiers>
  <relatedIdentifiers>
    <relatedIdentifier relatedIdentifierType="DOI" relationType="IsIdenticalTo">10.1097/CAD.0000000000000736</relatedIdentifier>
  </relatedIdentifiers>
  <rightsList>
    <rights rightsURI="http://www.opendefinition.org/licenses/cc-by">Creative Commons Attribution</rights>
    <rights rightsURI="info:eu-repo/semantics/openAccess">Open Access</rights>
  </rightsList>
  <descriptions>
    <description descriptionType="Abstract">A deeper understanding of the molecular basis of castration-resistant prostate cancer (CRPC) paved the way for the rational design and development of targeted therapies, which yielded promising preclinical results. However, translation of these potentially promising agents into clinics has usually failed, partly because of tumor heterogeneity. In this study, anticancer activities of the Bcl-2 inhibitor ABT-737 and the Akt-inhibitor erufosine (ErPC3) alone and in combination were compared between CRPC (PC-3 and DU-145) and healthy (PNT-1A) cell lines. The combination of ABT-737 and ErPC3 showed synergistic antiproliferative, antimigratory, and apoptotic effects in PC-3 cells. In DU-145 cells, ErPC3 showed a resistant profile, with half-maximal inhibitory concentration (IC50) values more than two-fold of PC-3, and combining ErPC3 with ABT-737 yielded no added benefit for all the incubation periods compared with ErPC3 alone. In PNT-1A cells, ABT-737 and ErPC3 alone and in combination reduced cell survival slightly and only at the highest concentrations. Apoptosis analysis showed that ABT-737 induced increased Akt expression and ErPC3 induced increased Mcl-1 expression in DU-145 cells. In conclusion, the ABT-737 and ErPC3 combination seems to be promising against CRPC, with a favorable safety profile in healthy cells. However, CRPC cell-type-specific resistance may be induced by enhancement of antiapoptotic signaling.</description>
  </descriptions>
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