Publication:
Unlocking Synergistic Potential: Agomelatine Enhances the Chemotherapeutic Effect of Paclitaxel in Breast Cancer Cell through MT1 Melatonin Receptors and ER-Alpha Axis

dc.authorscopusid57193431132
dc.authorscopusid58623155900
dc.authorscopusid55355223200
dc.authorwosidCinar, Irfan/Hpi-1003-2023
dc.authorwosidDincer, Busra/Hof-4015-2023
dc.contributor.authorDincer, Busra
dc.contributor.authorYildiztekin, Gizem
dc.contributor.authorCinar, Irfan
dc.contributor.authorIDDincer, Busra/0000-0002-3365-7741
dc.date.accessioned2025-12-11T00:54:29Z
dc.date.issued2023
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Dincer, Busra] Ondokuz Mayis Univ, Dept Pharmacol, Fac Pharm, TR-55100 Samsun, Turkiye; [Yildiztekin, Gizem] Erzincan Binali Yildirim Univ, Dept Pharmaceut Toxicol, Fac Pharm, TR-24100 Erzincan, Turkiye; [Cinar, Irfan] Kastamonu Univ, Dept Pharmacol, Fac Med, TR-37150 Kastamonu, Turkiyeen_US
dc.descriptionDincer, Busra/0000-0002-3365-7741;en_US
dc.description.abstractThis study investigates the potential of agomelatine (AGO), a synthetic melatoninergic drug, in combination with paclitaxel (PTX) for the treatment of breast cancer. The effects of AGO, PTX and melatonin (MTN) on breast cancer cell viability were investigated, focusing on the role of MT1 receptors. Cell viability and gene expression were analyzed in MCF-7 and MDA-MB-231 breast cancer cell experiments. The results show that AGO has cytotoxic effects on breast cancer cells similar to MTN. Combining AGO and MTN with PTX showed synergistic effects in MCF-7 cells. The study also reveals differences in the molecular mechanisms of breast cancer between estrogen-positive MCF-7 cells and estrogen-negative MDA-MB-231 cells. Combination with AGO and PTX affects apoptosis-associated proteins in both cell types. The findings suggest that AGO, combined with PTX, may be a promising adjuvant therapy for breast cancer and highlight the importance of MTN receptors in its mechanism of action.en_US
dc.description.sponsorshipResearch Fund of the Erzincan Binali Yildirim University, Turkey [TSA-2020-681]en_US
dc.description.sponsorshipThis work was supported by the Research Fund of the Erzincan Binali Yildirim University, Turkey. Project Number: TSA-2020-681. The authors extend their gratitude to Assoc. Prof. Ali DINCER for proofreading and Prof. Dr. Sukru BEYDEMIR for kind help in silico study.en_US
dc.description.woscitationindexScience Citation Index Expanded
dc.identifier.doi10.1002/cbdv.202301093
dc.identifier.issn1612-1872
dc.identifier.issn1612-1880
dc.identifier.issue10en_US
dc.identifier.pmid37690997
dc.identifier.scopus2-s2.0-85172655962
dc.identifier.scopusqualityQ4
dc.identifier.urihttps://doi.org/10.1002/cbdv.202301093
dc.identifier.urihttps://hdl.handle.net/20.500.12712/40170
dc.identifier.volume20en_US
dc.identifier.wosWOS:001074652200001
dc.identifier.wosqualityQ3
dc.language.isoenen_US
dc.publisherWiley-VCH Verlag GmbHen_US
dc.relation.ispartofChemistry & Biodiversityen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAntitumor Agentsen_US
dc.subjectCanceren_US
dc.subjectGene Expressionen_US
dc.subjectMedicinal Chemistryen_US
dc.titleUnlocking Synergistic Potential: Agomelatine Enhances the Chemotherapeutic Effect of Paclitaxel in Breast Cancer Cell through MT1 Melatonin Receptors and ER-Alpha Axisen_US
dc.typeArticleen_US
dspace.entity.typePublication

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