Synergistic role of thymoquinone and 5-fluorouracil in U-251MG glioblastoma cell line

Author:

Mutlu Altundağ Ergül1ORCID,Jannuzzi Ayşe Tarbin2ORCID,Özbilenler Cahit3ORCID,Ustürk Selma3ORCID,Altınoğlu Gülcem4ORCID

Affiliation:

1. Department of Biochemistry, Faculty of Medicine , Eastern Mediterranean University , Gazimağusa , Türkiye

2. Department of Pharmaceutical Toxicology, Faculty of Pharmacy , Istanbul University , Istanbul , Türkiye

3. Department of Chemistry, Faculty of Arts and Sciences , Eastern Mediterranean University , Famagusta , North Cyprus , Türkiye

4. Department of Neuroscience, Faculty of Medicine , Eastern Mediterranean University , Famagusta , North Cyprus , Türkiye

Abstract

Abstract Objectives Glioblastoma is a fast-growing and aggressive brain tumor. Despite the current treatment methods, such as chemical and surgical operations, the prognosis is still poor. Therefore, combined therapeutic strategies are proposed to maximize therapeutic efficacy and reduce toxicity. Thymoquinone has been shown to have neuroprotective effects in addition to its anti-cancer effects on different types of cancer. 5-Fluorouracil, on the other hand, is a cytotoxic chemotherapy agent used to treat cancer. As a synergistic combinational approach, this study aimed to examine the antiproliferative effects and production of reactive oxygen species in a glioblastoma cell line. Methods We have tested thymoquinone and 5-fluorouracil alone and in their combination to observe cellular growth with MTT assay. The combinational effects of the agents were determined by the CompuSYN software program. Cell proliferation was assayed with crystal violet assay. Reactive oxygen species production was analyzed by 2′,7′-dichlorodihydrofluorescein diacetate in glioblastoma cells. Results Thymoquinone and 5-fluorouracil inhibited cell growth of glioblastoma cells with half maximal inhibitory concentrations (IC50) of 45.93 and 14.02 µM for 48 h, respectively. At synergistic combinational concentrations, the crystal violet assay demonstrated that there is a positive correlation between combination index values and cell proliferation. Also, an increment in the production of reactive oxygen species was observed upon combinational treatments. Conclusions Our results indicate that the combinational strategy of these two agents reduced cell viability and proliferation in glioblastoma cells and showed strong synergistic anticancer efficiency.

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry (medical),Clinical Biochemistry,Molecular Biology,Biochemistry

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