
<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/">
  <dc:type>info:eu-repo/semantics/conferenceProceedings</dc:type>
  <dc:subject xml:lang="eng">Keywords : fibrosarcoma, hamsters, repurposed drugs, NF-kB, ROS.</dc:subject>
  <dc:description xml:lang="eng">Abstract:
 Transcription factor NF-kB acts as an important target in oncology, as most of the molecules formed by transcription of genes trigger cancers. Also, ROS (Reactive Oxygen Species) activity is interconnected with NF-kB and cancer development. To identify NF-kB inhibition and/or ROS stimulation as antitumor mechanisms, we have screened combinations of currently approved non-oncological repurposed drugs that can inhibit hamster fibrosarcoma growth by rescuing cancer development with NF-kB stimulation and/or ROS inhibition.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:format>759473 bytes</dc:format>
  <dc:language>eng</dc:language>
  <dc:identifier>https://phaidrabg.bg.ac.rs/o:31329</dc:identifier>
  <dc:identifier>cobiss:126492937</dc:identifier>
  <dc:title xml:lang="eng">Aniticancer mechanisms of repurposed drugs in oncology on hamster model</dc:title>
  <dc:rights>All rights reserved</dc:rights>
  <dc:date>2023</dc:date>
  <dc:creator id="https://orcid.org/0000-0001-7895-9009">Popović, Kosta J.</dc:creator>
  <dc:creator id="https://orcid.org/0000-0001-7880-0874">Popović, Dušica J.</dc:creator>
  <dc:creator id="https://orcid.org/0000-0002-7739-5202">Miljković, Dejan</dc:creator>
  <dc:creator id="https://orcid.org/0000-0002-0760-9180">Lalošević, Dušan</dc:creator>
  <dc:creator id="https://orcid.org/0000-0003-0457-3087 https://plus.cobiss.net/cobiss/sr/sr/conor/2237799">Dolićanin, Zana</dc:creator>
  <dc:creator id="https://orcid.org/0000-0001-7531-5099">Čapo, Ivan</dc:creator>
  <dc:creator id="https://orcid.org/0000-0002-6790-8668">Popović, Jovan K.</dc:creator>
  <dc:source>JCMST 2023 - The 2nd PSU-UNS Joint Conference on Medical Science and Technology, 11-13 October 2023(2)</dc:source>
</oai_dc:dc>
