Anticancer, antioxidant activities and molecular docking study of thiazolidine-4-one and thiadiazol derivatives

Abstract

Liver cancer accounts for a major portion of the global cancer burden. In many nations, the prevalence of this condition has risen in recent decades. New series of thiazolidinones and thiadiazolidine have been designed, synthesized, and evaluated for potential antioxidant and antihepatocarcinogenic activity. The antioxidant activity was evaluated using a DPPH assay. Furthermore, we examined the compounds against Hepg-2 cells using MTT assay, flow cytometry analysis through the cell cycle, reactive oxygen species, and apoptosis. The result showed that compound 6b has the highest antioxidant activity with IC₅₀ = 60.614 ± 0.739 µM. The anticancer activity showed that compounds 5 and 6b have significant toxicity against liver cancer cells Hepg2, IC₅₀ values (9.082 and 4.712) µM, respectively. Flow cytometry experiments revealed that compound 5 arrested Hepg-2 cells in the S process, while compound 6b arrested Hepg-2 cells in the G1. Compound 6b had a greater reduction in reactive oxygen species and late apoptosis than compound 5. Substantially, compound 5 had affinity energies of –7.6 and –8.5 for Akt and CDK4 proteins, respectively, but compound 6b had affinity energies of –7.8 and –10.1 for Akt1 and CDK4 proteins, respectively. Consequently, compound 6b had lower binding energies than compound 5. In this work, we used multiple bioinformatics methods to shed light on the prospective therapeutic use of these series as novel candidates to target immune cells in the tumor microenvironment of hepatocellular carcinomas such as CD8+ T cells, endothelial cells, and hematopoietic stem cells.

Communicated by Ramaswamy H. Sarma

Keywords:

• HepG-2
• thaiazolidinone
• AKT1
• CDK4
• apoptosis
• cell cycle
• bioinformatics immunomodulation

Disclosure statement

All authors declare that there are no conflicts of interest.

Acknowledgments

The authors are gratefully to Prof. Dr. Ali Alshawi to review discuss the flow cytometry experiments

Funding

The author(s) reported there is no funding associated with the work featured in this article.