Publication:
Green Synthesis, Characterization of Melatonin-Like Drug Bioconjugated COS Quantum Dots and Its Antiproliferative Effect on Different Cancer Cells

dc.authorscopusid57559330400
dc.authorscopusid6506121388
dc.authorscopusid6602395368
dc.contributor.authorBalpınar, Ö.
dc.contributor.authorNadaroǧlu, H.
dc.contributor.authorHacimüftüoǧlu, A.
dc.date.accessioned2025-12-11T00:32:10Z
dc.date.issued2023
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Balpınar] Özge, Hemp Research Institute, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Nadaroǧlu] Hayrünnisa, Department of Nanoscience and Nanoengineering, Atatürk Üniversitesi, Erzurum, Erzurum, Turkey; [Hacimüftüoǧlu] Ahmet, Department of Medical Pharmacology, Ataturk University, Faculty of Medicine, Erzurum, Turkeyen_US
dc.description.abstractBackground: Quantum dots are usually particles smaller than 100 nm and have a low toxic effect. This study aimed to bioconjugate the anticancer effective melatonin agonist to quantum dots and demonstrate its effects in two cancer lines. This is the first study that aims to examine the anticancer activity of ramelteon bioconjugation to quantum dots, providing a new perspective on the use of Melatonin and its derivatives in cancer. Methods and Results: For this purpose, first of all, cobalt sulfide (CoS) quantum dots were synthesized, bioconjugated and characterized with Punica granatum extract by green synthesis method. The effects of synthesized nanomaterials on neuroblastoma and prostate cancer cells were investigated. It was noted that nanomaterials reduced cell viability by 50% in neuroblastoma and prostate cancer lines at a dose of 50 µg/mL. Ramelteon bioconjugated nanomaterials reduced cancer cell viability by 1.4 times more than free melatonin. CoS quantum dots were determined to double the oxidative stress in the neuroblastoma cell line compared to the control, while no change was observed in prostate cancer. In the gene expression findings, it was observed that CoS nanoparticles caused an increase in the expression levels of apoptosis-related genes in the neuroblastoma cell line and induced key protein expression levels of pathways such as ROR-alpha in the prostate cancer cell line. Conclusion: As a result, it was observed that the viability of the neuroblastoma cell line decreased with apoptosis induced by oxidative stress, while this effect was observed in the DU-145 cell line via the ROR-alpha pathway. © 2023, The Author(s), under exclusive licence to Springer Nature B.V.en_US
dc.identifier.doi10.1007/s11033-023-08817-3
dc.identifier.endpage9151en_US
dc.identifier.issn0301-4851
dc.identifier.issn1573-4978
dc.identifier.issue11en_US
dc.identifier.pmid37768465
dc.identifier.scopus2-s2.0-85172882493
dc.identifier.scopusqualityQ3
dc.identifier.startpage9143en_US
dc.identifier.urihttps://doi.org/10.1007/s11033-023-08817-3
dc.identifier.urihttps://hdl.handle.net/20.500.12712/37145
dc.identifier.volume50en_US
dc.identifier.wosqualityQ3
dc.language.isoenen_US
dc.publisherSpringer Science and Business Media B.V.en_US
dc.relation.ispartofMolecular Biology Reportsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBioconjugationen_US
dc.subjectCanceren_US
dc.subjectMelatoninen_US
dc.subjectQuantum Doten_US
dc.titleGreen Synthesis, Characterization of Melatonin-Like Drug Bioconjugated COS Quantum Dots and Its Antiproliferative Effect on Different Cancer Cellsen_US
dc.typeArticleen_US
dspace.entity.typePublication

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