- Düzce Tıp Fakültesi Dergisi
- Volume:25 Issue:3
- Muscarinic Receptors as Targets for Metronomic Therapy in Ovarian Cancer
Muscarinic Receptors as Targets for Metronomic Therapy in Ovarian Cancer
Authors : Fatma Söylemez, Çağatay Han Türkseven
Pages : 225-230
Doi:10.18678/dtfd.1315416
View : 85 | Download : 137
Publication Date : 2023-12-30
Article Type : Research Paper
Abstract :Aim: In this study, the effects of muscarinic acetylcholine receptor (mAChR) agonist carbachol on the proliferation of cisplatin-resistant (A2780cis) and cisplatin-free (SKOV-3) ovarian cancer cell line were for the first time investigated to further evaluate the potential therapeutic effect of metronomic chemotherapy. Material and Methods: The inhibitory effect of carbachol on cell proliferation was detected using the xCELLigence Real-Time Cell Analyzer (RTCA) dual plate (DP) system. A preliminary study was conducted to determine the dose of carbachol 100 µM, cisplatin 1 µM, and two combination studies were carried out with 100 µM carbachol + cisplatin 1 µM and 100 µM carbachol + 10 µM atropine, over cancer cells without drugs was used as the control group. The cell proliferation curve was monitored for 96 hours. The cell index value of inhibition in cell proliferation was automatically measured every hour for each well using RTCA 1.2.1 software. Results: Co-administration of carbachol with cisplatin caused a decrease in cell number in both A2780cis and SKOV-3 cell lines in a time-dependent manner (p<0.001). Substantial cell death was observed in both cisplatin-resistant (A2780cis) and cisplatin-free (SKOV-3) cell lines within 24 hours after carbachol with cisplatin application and this continued at the 96th hour. Conclusion: The findings of this study confirm the notion that mAChRs can be considered as therapeutic targets for metronomic therapy in ovarian cancer, as well as the usefulness of a muscarinic agonist as a repositioning drug in the treatment of such tumors.Keywords : Yumurtalık kanseri, mAChR, Karbakol, SKOV 3, A2780CIS, Sisplatin