Evaluation of the Anticancer and Biological Activities of Istaroxime via Ex Vivo Analyses, Molecular Docking and Conceptual Density Functional Theory Computations

dc.authorid0000-0001-8623-784Xtr
dc.contributor.authorCanturk, Pakize
dc.contributor.authorGok, Ege
dc.contributor.authorUnal, Naz
dc.contributor.authorGungor, Burcin
dc.contributor.authorKarakus, Gulderen
dc.contributor.authorKaya, Savas
dc.contributor.authorKatin, Konstantin P.
dc.date.accessioned2024-02-26T07:37:46Z
dc.date.available2024-02-26T07:37:46Z
dc.date.issued7 November 2023tr
dc.departmentEczacılık Fakültesitr
dc.description.abstractCancer is a disease that occurs as a result of abnormal or uncontrolled growth of cells due to DNA damage, among many other causes. Certain cancer treatments aim to increase the excess of DNA breaks to such an extent that they cannot escape from the general mechanism of cell checkpoints, leading to the apoptosis of mutant cells. In this study, one of the Sarco-endoplasmic reticulum Ca2+ATPase (SERCA2a) inhibitors, Istaroxime, was investigated. There has been very limited number of articles so far reporting Istaroxime’s anticancer activity; thus, we aimed to evaluate the anticancer effects of Istaroxime by cell proliferation assay and revealed the cytotoxic activity of the compound. We further determined the interaction of Istaroxime with topoisomerase enzymes through enzyme activity tests and detailed molecular modeling analysis. Istaroxime exhibited an antiproliferative effect on A549, MCF7, and PC3 cell lines and inhibited Topoisomerase I, suggesting that Istaroxime can act as a Topoisomerase I inhibitor under in vitro conditions. Molecular docking analysis supported the experimental observations. A chemical reactivity analysis of the Istaroxime molecule was made in the light of Density Functional Theory computations. For this aim, important chemical reactivity descriptors such as hardness, electronegativity, and electrophilicity were computed and discussed as detailed.tr
dc.description.sponsorshipTÜBİTAK-BİDEP2209Atr
dc.identifier.citationExport citation file: BibTeX | EndNote | RIS MDPI and ACS Style Gok, E.; Unal, N.; Gungor, B.; Karakus, G.; Kaya, S.; Canturk, P.; Katin, K.P. Evaluation of the Anticancer and Biological Activities of Istaroxime via Ex Vivo Analyses, Molecular Docking and Conceptual Density Functional Theory Computations. Molecules 2023, 28, 7458. https://doi.org/10.3390/molecules28227458 AMA Style Gok E, Unal N, Gungor B, Karakus G, Kaya S, Canturk P, Katin KP. Evaluation of the Anticancer and Biological Activities of Istaroxime via Ex Vivo Analyses, Molecular Docking and Conceptual Density Functional Theory Computations. Molecules. 2023; 28(22):7458. https://doi.org/10.3390/molecules28227458 Chicago/Turabian Style Gok, Ege, Naz Unal, Burcin Gungor, Gulderen Karakus, Savas Kaya, Pakize Canturk, and Konstantin P. Katin. 2023. "Evaluation of the Anticancer and Biological Activities of Istaroxime via Ex Vivo Analyses, Molecular Docking and Conceptual Density Functional Theory Computations" Molecules 28, no. 22: 7458. https://doi.org/10.3390/molecules28227458tr
dc.identifier.doi10.3390/molecules28227458en_US
dc.identifier.endpage7458tr
dc.identifier.issue22tr
dc.identifier.pmid38005181en_US
dc.identifier.scopus2-s2.0-85177742077en_US
dc.identifier.scopusqualityN/A
dc.identifier.startpage7458tr
dc.identifier.urihttps://www.mdpi.com/1420-3049/28/22/7458
dc.identifier.urihttps://hdl.handle.net/20.500.12418/14311
dc.identifier.volume28tr
dc.identifier.wosWOS:001113726800001en_US
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherMDPItr
dc.relation.ispartofMoleculesen_US
dc.relation.publicationcategoryUluslararası Editör Denetimli Dergide Makaletr
dc.relation.tubitakBİDEP2209A-1919B011701733
dc.rightsinfo:eu-repo/semantics/openAccesstr
dc.subjectIstaroxime; Topoisomerase enzymes; Anticancer drugs; Density Functional Theorytr
dc.titleEvaluation of the Anticancer and Biological Activities of Istaroxime via Ex Vivo Analyses, Molecular Docking and Conceptual Density Functional Theory Computationsen_US
dc.typeArticleen_US

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