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2-Pyrazoline-5-One Derivative Suppresses Cell Proliferation and Induces Apoptosis With Upregulation of Bax in Breast
Sevgi Kocyigit Sevinc1, Ş Güniz Küçükgüzel2, Sevim Rollas3
1Faculty of Medicine, Biophysics Department, Kütahya Health Sciences University, Kütahya, Turkey.
Abstract:
The most common cancer in women worldwide is still breast cancer. Among its subtypes, luminal A and triple-negative breast cancers present significant therapeutic challenges due to intrinsic drug resistance and absence of effective targeted treatments. The pharmacological potential of heterocyclic compounds has garnered more attention in recent years, and structures like pyrazolines, hydrazones, and triazoles are important in the development of new drugs. Compounds incorporating these scaffolds have been shown in numerous studies to have strong anticancer action. In this regard, pyrazoline derivatives have become a viable field of study for focused treatment approaches. This study focused on evaluating the cytotoxic potential of the 2-pyrazoline-5-one derivative compound against luminal-A (MCF-7) and triple-negative (MDA-MB-231) breast cancer cell lines. The CCK-8 test was used to assess the impact on cell viability. Additionally, Annexin V/PI staining was used to identify the apoptotic effects, and fluorescence microscopy was used for analysis. The wound healing experiment was used to measure the capacity of cells to migrate, and migration process was monitored following scratch formation. The colony formation assay was used to assess the potential for cell proliferation, and clonal growth capacities were compared. Bax protein levels in compound-treated cancer cells were quantified by ELISA to investigate the apoptotic mechanism. IC50 values in MCF-7 and MDA-MB-231 cell lines were used to evaluate the cytotoxic effects of the 2-pyrazoline-5-one derivative. The compound exhibited strong cytotoxic activity and reduced cell viability in both cell lines in a concentration-dependent manner, with IC50 values of 13 µM in MCF-7 cells and 16 µM in MDA-MB-231 cell. Furthermore, the compound effectively induced apoptosis and significantly suppressed colony formation and cell migration in both cell lines. Additionally, it showed a concentration-dependent rise in Bax protein levels, suggesting a pro-apoptotic action. These results confirm that the 2-pyrazoline-5-one derivative has strong antiproliferative and pro-apoptotic activity through Bax activation, providing a possible pathway for the creation of targeted treatments for breast cancer.
Insights
A novel 2-pyrazoline-5-one derivative shows potent anticancer effects against challenging breast cancer subtypes. This compound effectively reduced cell viability, induced apoptosis, and inhibited migration and proliferation in luminal A and triple-negative breast cancer cells.
Area of Science:
- Medicinal Chemistry
- Oncology
- Pharmacology
Background:
- Breast cancer, particularly luminal A and triple-negative subtypes, poses significant therapeutic challenges due to drug resistance and lack of targeted treatments.
- Heterocyclic compounds, including pyrazolines, hydrazones, and triazoles, are increasingly recognized for their potent anticancer properties.
- Pyrazoline derivatives represent a promising area for developing novel breast cancer therapies.
Purpose of the Study:
- To evaluate the cytotoxic potential of a specific 2-pyrazoline-5-one derivative against luminal A (MCF-7) and triple-negative (MDA-MB-231) breast cancer cell lines.
- To investigate the compound's effects on cell viability, apoptosis, migration, and proliferation.
- To explore the underlying apoptotic mechanism, specifically focusing on Bax protein levels.
Main Methods:
- Cytotoxicity was assessed using the CCK-8 assay to determine IC50 values.
- Apoptosis was analyzed via Annexin V/PI staining and fluorescence microscopy.
- Cell migration and proliferation were evaluated using wound healing and colony formation assays, respectively. Bax protein levels were quantified by ELISA.
Main Results:
- The 2-pyrazoline-5-one derivative demonstrated significant cytotoxic activity against both MCF-7 (IC50 = 13 µM) and MDA-MB-231 (IC50 = 16 µM) cell lines in a dose-dependent manner.
- The compound effectively induced apoptosis, suppressed cell migration, and inhibited colony formation in both tested breast cancer cell lines.
- A concentration-dependent increase in Bax protein levels was observed, indicating a pro-apoptotic mechanism.
Conclusions:
- The 2-pyrazoline-5-one derivative exhibits strong antiproliferative and pro-apoptotic activity against luminal A and triple-negative breast cancer cells.
- The observed pro-apoptotic effect is mediated, at least in part, by the activation of Bax.
- This compound represents a potential candidate for the development of targeted therapies for challenging breast cancer subtypes.
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