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High Copper Complex Stability and Slow Reduction Kinetics as Key Parameters for Improved Activity, Paraptosis Induction, and Impact on Drug-Resistant Cells of Anticancer Thiosemicarbazones

  • Sonja Hager
  • , Veronika F. S. Pape
  • , Vivien Posa
  • , Bianca Montsch
  • , Lukas Uhlik
  • , Gergely Szakacs
  • , Szilard Toth
  • , Nikolett Jabronka
  • , Bernhard K. Keppler
  • , Christian R. Kowol
  • , Eva A. Enyedy (Corresponding author)
  • , Petra Heffeter (Corresponding author)

Publications: Contribution to journalArticlePeer Reviewed

Original languageEnglish
Pages (from-to)395-414
Number of pages20
JournalAntioxidants and Redox Signaling
Volume33
Issue number6
DOIs
Publication statusPublished - 9 Jun 2020

Funding

This work was supported by the National Research, Development and Innovation Office-NKFI through project FK 124240 and FIKP program TUDFO/47138-1/2019-ITM. Furthermore, this work was in part funded by the Austrian Science Fund (FWF) grant number P31923 (to C.R. Kowol and P. Heffeter) as well as by the bilateral program Scientific and Technological Cooperation of the OeAD. Part of the data was generated in course of the research exchange program Aktion ``Osterreich-Ungarn'' as well as in a short-term fellowship of the European Molecular Biology Organization (EMBO, grant ASTF335-2016) both to P. Heffeter. S. Hager is a recipient of a DOC Fellowship of the Austrian Academy of Sciences. The funding sources had no involvement in the collection, analysis, and interpretation of data as well as in the decision to submit the article for publication.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Austrian Fields of Science 2012

  • 302014 Endocrinology
  • 301904 Cancer research
  • 106002 Biochemistry
  • 106023 Molecular biology

Keywords

  • solution stability
  • thiosemicarbazones
  • copper complexes
  • protein disulfide isomerase
  • paraptosis
  • superoxide dismutase
  • BIOLOGICAL EVALUATION
  • IN-VITRO
  • PHASE-I
  • TRIAPINE
  • IRON
  • DI-2-PYRIDYLKETONE
  • IDENTIFICATION
  • METABOLISM
  • STRESS
  • DP44MT

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