Number of the records: 1  

Ferrocenes as new anticancer drug candidates: Determination of the mechanism of action

  1. 1.
    0519357 - ÚFCH JH 2021 RIV NL eng J - Journal Article
    Skoupilová, H. - Bartošík, M. - Sommerová, L. - Pinkas, Jiří - Vaculovič, T. - Kanický, V. - Karban, Jindřich - Hrstka, R.
    Ferrocenes as new anticancer drug candidates: Determination of the mechanism of action.
    European Journal of Pharmacology. Roč. 867, JAN 2020 (2020), č. článku 172825. ISSN 0014-2999. E-ISSN 1879-0712
    R&D Projects: GA ČR(CZ) GA17-05838S
    Institutional support: RVO:61388955 ; RVO:67985858
    Keywords : transferrin * iron * ferroquine * cisplatin * Ferrocene * Ovarian cancer * Cellular uptake * Transferrin * Transferrin receptor * Reactive oxygen species
    OECD category: Physical chemistry; Organic chemistry (UCHP-M)
    Impact factor: 4.432, year: 2020
    Method of publishing: Limited access

    Chemotherapy plays an essential role in the management of cancer worldwide. However, it is a non-specific treatment limited by major drawbacks, thus identification and testing of new promising molecular structures representing potential drug candidates are urgently needed. In this work, ferrocene complexes as potential antitumor drugs that display cytotoxicity in low micromolar concentrations against ovarian cancer cells A2780 and SK-OV-3 were investigated to identify their mode of action. Their mechanism of cellular accumulation was studied using differential pulse voltammetry and inductively coupled plasma mass spectrometry. Their mode of cell death induction was determined by changes in the mitochondrial membrane potential, production of reactive oxygen species and by Annexin V staining.
    Permanent Link: http://hdl.handle.net/11104/0304348

     
    FileDownloadSizeCommentaryVersionAccess
    Eur_J_Pharm_2020_Skoupilova_et_al.pdf2858 KBPublisher’s postprintrequire
    0519357.pdf1858.1 KBPublisher’s postprintrequire
     
Number of the records: 1  

  This site uses cookies to make them easier to browse. Learn more about how we use cookies.