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

ArticleAçık Erişim

Özet

This 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. © 2023 Wiley-VHCA AG, Zurich, Switzerland.

Anahtar Kelimeler

RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/11957Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1002/cbdv.202301093Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorDincer, Busra
dc.contributor.authorYildiztekin, Gizem
dc.contributor.authorCinar, Irfan
dc.date.accessioned2026-10-18T20:26:55.834760743Z
dc.date.available2026-10-18T20:26:55.834760743Z
dc.date.issued2023
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. © 2023 Wiley-VHCA AG, Zurich, Switzerland.
dc.description.sponsorshipThis work was supported by the Research Fund of the Erzincan Binali Yıldırım University, Turkey. Project Number: TSA‐2020‐681. The authors extend their gratitude to Assoc. Prof. Ali DINCER for proofreading and Prof. Dr. Şükrü BEYDEMIR for kind help in silico study.
dc.identifier.doi10.1002/cbdv.202301093
dc.identifier.eissn1612-1880
dc.identifier.issn1612-1872
dc.identifier.issue10
dc.identifier.pmid37690997
dc.identifier.scopus2-s2.0-85172655962
dc.identifier.startpagee202301093
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/11957
dc.identifier.volume20
dc.identifier.wosWOS:001074652200001
dc.language.isoen
dc.publisherJohn Wiley and Sons Inc
dc.relation.ispartofChemistry and Biodiversity
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectantitumor agents
dc.subjectcancer
dc.subjectgene expression
dc.subjectmedicinal chemistry
dc.subjectAcetamides
dc.subjectAntineoplastic Agents
dc.subjectAntineoplastic Agents, Phytogenic
dc.subjectApoptosis
dc.subjectBreast Neoplasms
dc.subjectCell Line, Tumor
dc.subjectCell Proliferation
dc.subjectCell Survival
dc.subjectDose-Response Relationship, Drug
dc.subjectDrug Screening Assays, Antitumor
dc.subjectDrug Synergism
dc.subjectEstrogen Receptor alpha
dc.subjectFemale
dc.subjectHumans
dc.subjectMCF-7 Cells
dc.subjectMelatonin
dc.subjectNaphthalenes
dc.subjectPaclitaxel
dc.subjectReceptor, Melatonin, MT1
dc.subjectagomelatine
dc.subjectmelatonin 1 receptor
dc.subjectacetamide derivative
dc.subjectantineoplastic agent
dc.subjectESR1 protein, human
dc.subjectnaphthalene derivative
dc.subjectArticle
dc.titleUnlocking Synergistic Potential: Agomelatine Enhances the Chemotherapeutic Effect of Paclitaxel in Breast Cancer Cell Through MT1 Melatonin Receptors and ER-alpha Axis
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus2
rdl.citation.wos1
rdl.departmentDepartment of Pharmaceutical Toxicology, Faculty of Pharmacy, Erzincan Binali Yildirim University, Erzincan, 24100, Turkey.
rdl.oa.statusopen
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)