Unlocking Synergistic Potential: Agomelatine Enhances the Chemotherapeutic Effect of Paclitaxel in Breast Cancer Cell Through MT1 Melatonin Receptors and ER-alpha Axis
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
Tam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | Dincer, Busra | |
| dc.contributor.author | Yildiztekin, Gizem | |
| dc.contributor.author | Cinar, Irfan | |
| dc.date.accessioned | 2026-10-18T20:26:55.834760743Z | |
| dc.date.available | 2026-10-18T20:26:55.834760743Z | |
| dc.date.issued | 2023 | |
| dc.description.abstract | 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. | |
| dc.description.sponsorship | This 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.doi | 10.1002/cbdv.202301093 | |
| dc.identifier.eissn | 1612-1880 | |
| dc.identifier.issn | 1612-1872 | |
| dc.identifier.issue | 10 | |
| dc.identifier.pmid | 37690997 | |
| dc.identifier.scopus | 2-s2.0-85172655962 | |
| dc.identifier.startpage | e202301093 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/ebyu/11957 | |
| dc.identifier.volume | 20 | |
| dc.identifier.wos | WOS:001074652200001 | |
| dc.language.iso | en | |
| dc.publisher | John Wiley and Sons Inc | |
| dc.relation.ispartof | Chemistry and Biodiversity | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.subject | antitumor agents | |
| dc.subject | cancer | |
| dc.subject | gene expression | |
| dc.subject | medicinal chemistry | |
| dc.subject | Acetamides | |
| dc.subject | Antineoplastic Agents | |
| dc.subject | Antineoplastic Agents, Phytogenic | |
| dc.subject | Apoptosis | |
| dc.subject | Breast Neoplasms | |
| dc.subject | Cell Line, Tumor | |
| dc.subject | Cell Proliferation | |
| dc.subject | Cell Survival | |
| dc.subject | Dose-Response Relationship, Drug | |
| dc.subject | Drug Screening Assays, Antitumor | |
| dc.subject | Drug Synergism | |
| dc.subject | Estrogen Receptor alpha | |
| dc.subject | Female | |
| dc.subject | Humans | |
| dc.subject | MCF-7 Cells | |
| dc.subject | Melatonin | |
| dc.subject | Naphthalenes | |
| dc.subject | Paclitaxel | |
| dc.subject | Receptor, Melatonin, MT1 | |
| dc.subject | agomelatine | |
| dc.subject | melatonin 1 receptor | |
| dc.subject | acetamide derivative | |
| dc.subject | antineoplastic agent | |
| dc.subject | ESR1 protein, human | |
| dc.subject | naphthalene derivative | |
| dc.subject | Article | |
| dc.title | Unlocking Synergistic Potential: Agomelatine Enhances the Chemotherapeutic Effect of Paclitaxel in Breast Cancer Cell Through MT1 Melatonin Receptors and ER-alpha Axis | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| rdl.citation.scopus | 2 | |
| rdl.citation.wos | 1 | |
| rdl.department | Department of Pharmaceutical Toxicology, Faculty of Pharmacy, Erzincan Binali Yildirim University, Erzincan, 24100, Turkey. | |
| rdl.oa.status | open | |
| rdl.source.index | SCOPUS | |
| rdl.source.index | WOS | |
| rdl.source.index | PUBMED | |
| rdl.wos.index | Science Citation Index Expanded (SCI-EXPANDED) |
