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Investigation of Anticancer Properties of Monoterpene-Aminopyrimidine Hybrids on A2780 Ovarian Cancer Cells.
Nagy, Viktória; Mounir, Raji; Szebeni, Gábor J; Szakonyi, Zsolt; Gémes, Nikolett; Minorics, Renáta; Germán, Péter; Zupkó, István.
Afiliação
  • Nagy V; Institute of Pharmacodynamics and Biopharmacy, University of Szeged, H-6720 Szeged, Hungary.
  • Mounir R; Institute of Pharmaceutical Chemistry, University of Szeged, H-6720 Szeged, Hungary.
  • Szebeni GJ; Laboratory of Functional Genomics, Eötvös Loránd Research Network Biological Research Centre, Institute of Genetics, H-6726 Szeged, Hungary.
  • Szakonyi Z; Institute of Pharmaceutical Chemistry, University of Szeged, H-6720 Szeged, Hungary.
  • Gémes N; Interdisciplinary Centre of Natural Products, University of Szeged, H-6720 Szeged, Hungary.
  • Minorics R; Laboratory of Functional Genomics, Eötvös Loránd Research Network Biological Research Centre, Institute of Genetics, H-6726 Szeged, Hungary.
  • Germán P; Institute of Pharmacodynamics and Biopharmacy, University of Szeged, H-6720 Szeged, Hungary.
  • Zupkó I; Institute of Pharmacodynamics and Biopharmacy, University of Szeged, H-6720 Szeged, Hungary.
Int J Mol Sci ; 24(13)2023 Jun 24.
Article em En | MEDLINE | ID: mdl-37445759
ABSTRACT
The present study aimed to characterize the antiproliferative and antimetastatic properties of two recently synthesized monoterpene-aminopyrimidine hybrids (1 and 2) on A2780 ovary cancer cells. Both agents exerted a more pronounced cell growth inhibitory action than the reference agent cisplatin, as determined by the MTT assay. Tumor selectivity was assessed using non-cancerous fibroblast cells. Hybrids 1 and 2 induced changes in cell morphology and membrane integrity in A2780 cells, as evidenced by Hoechst 33258-propidium iodide fluorescent staining. Cell cycle analysis by flow cytometry revealed substantial changes in the distribution of A2780 ovarian cancer cells, with an increased rate in the subG1 and G2/M phases, at the expense of the G1 cell population. Moreover, the tested molecules accelerated tubulin polymerization in a cell-free in vitro system. The antimetastatic properties of both tested compounds were investigated by wound healing and Boyden chamber assays after 24 and 48 h of incubation. Treatment with 1 and 2 resulted in time- and concentration-dependent inhibition of migration and invasion of A2780 cancer cells. These results support that the tested agents may be worth of further investigation as promising anticancer drug candidates.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Antineoplásicos Limite: Female / Humans Idioma: En Revista: Int J Mol Sci Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Hungria

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Antineoplásicos Limite: Female / Humans Idioma: En Revista: Int J Mol Sci Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Hungria