Investigation of Anticancer Properties of Monoterpene-Aminopyrimidine Hybrids on A2780 Ovarian Cancer Cells

The present study aimed to characterize the antiproliferative and antimetastatic properties of two recently synthesized monoterpene-aminopyrimidine hybrids (<b>1</b> and <b>2</b>) on A2780 ovary cancer cells. Both agents exerted a more pronounced cell growth inhibitory action...

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Main Authors: Viktória Nagy, Raji Mounir, Gábor J. Szebeni, Zsolt Szakonyi, Nikolett Gémes, Renáta Minorics, Péter Germán, István Zupkó
Format: Article
Language:English
Published: MDPI AG 2023-06-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/24/13/10581
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author Viktória Nagy
Raji Mounir
Gábor J. Szebeni
Zsolt Szakonyi
Nikolett Gémes
Renáta Minorics
Péter Germán
István Zupkó
author_facet Viktória Nagy
Raji Mounir
Gábor J. Szebeni
Zsolt Szakonyi
Nikolett Gémes
Renáta Minorics
Péter Germán
István Zupkó
author_sort Viktória Nagy
collection DOAJ
description The present study aimed to characterize the antiproliferative and antimetastatic properties of two recently synthesized monoterpene-aminopyrimidine hybrids (<b>1</b> and <b>2</b>) 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 <b>1</b> and <b>2</b> 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 <b>1</b> and <b>2</b> 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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spelling doaj.art-3543d74e3e7647bb811aea7228bb4dd02023-11-18T16:40:21ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672023-06-0124131058110.3390/ijms241310581Investigation of Anticancer Properties of Monoterpene-Aminopyrimidine Hybrids on A2780 Ovarian Cancer CellsViktória Nagy0Raji Mounir1Gábor J. Szebeni2Zsolt Szakonyi3Nikolett Gémes4Renáta Minorics5Péter Germán6István Zupkó7Institute of Pharmacodynamics and Biopharmacy, University of Szeged, H-6720 Szeged, HungaryInstitute of Pharmaceutical Chemistry, University of Szeged, H-6720 Szeged, HungaryLaboratory of Functional Genomics, Eötvös Loránd Research Network Biological Research Centre, Institute of Genetics, H-6726 Szeged, HungaryInstitute of Pharmaceutical Chemistry, University of Szeged, H-6720 Szeged, HungaryLaboratory of Functional Genomics, Eötvös Loránd Research Network Biological Research Centre, Institute of Genetics, H-6726 Szeged, HungaryInstitute of Pharmacodynamics and Biopharmacy, University of Szeged, H-6720 Szeged, HungaryInstitute of Pharmacodynamics and Biopharmacy, University of Szeged, H-6720 Szeged, HungaryInstitute of Pharmacodynamics and Biopharmacy, University of Szeged, H-6720 Szeged, HungaryThe present study aimed to characterize the antiproliferative and antimetastatic properties of two recently synthesized monoterpene-aminopyrimidine hybrids (<b>1</b> and <b>2</b>) 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 <b>1</b> and <b>2</b> 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 <b>1</b> and <b>2</b> 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.https://www.mdpi.com/1422-0067/24/13/10581monoterpeneaminoalcoholantiproliferativeG2/M arrestantimetastaticovarian cancer
spellingShingle Viktória Nagy
Raji Mounir
Gábor J. Szebeni
Zsolt Szakonyi
Nikolett Gémes
Renáta Minorics
Péter Germán
István Zupkó
Investigation of Anticancer Properties of Monoterpene-Aminopyrimidine Hybrids on A2780 Ovarian Cancer Cells
International Journal of Molecular Sciences
monoterpene
aminoalcohol
antiproliferative
G2/M arrest
antimetastatic
ovarian cancer
title Investigation of Anticancer Properties of Monoterpene-Aminopyrimidine Hybrids on A2780 Ovarian Cancer Cells
title_full Investigation of Anticancer Properties of Monoterpene-Aminopyrimidine Hybrids on A2780 Ovarian Cancer Cells
title_fullStr Investigation of Anticancer Properties of Monoterpene-Aminopyrimidine Hybrids on A2780 Ovarian Cancer Cells
title_full_unstemmed Investigation of Anticancer Properties of Monoterpene-Aminopyrimidine Hybrids on A2780 Ovarian Cancer Cells
title_short Investigation of Anticancer Properties of Monoterpene-Aminopyrimidine Hybrids on A2780 Ovarian Cancer Cells
title_sort investigation of anticancer properties of monoterpene aminopyrimidine hybrids on a2780 ovarian cancer cells
topic monoterpene
aminoalcohol
antiproliferative
G2/M arrest
antimetastatic
ovarian cancer
url https://www.mdpi.com/1422-0067/24/13/10581
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