Potassium Benzoate Induced Cytotoxicity via Alteration of Gene Expression-Associated Apoptosis and Cell Cycle Genes in Tumor Cell Lines

Document Type : Original Article

Authors

1 Department of Genetics, Faculty of Agriculture, Ain Shams University, Cairo, Egypt.

2 Department of Medical Support, Al-Karak University College, Al-Balqa Applied University, Jordan.

3 Department of Agriculture Microbiology, Faculty of Agriculture, Ain Shams University, Cairo, Egypt.

4 Medical Genetic Center, Faculty of Medicine, Ain Shams University, Cairo, Egypt.

10.21608/eajbsc.2024.386696

Abstract

Certain food preservatives, including potassium benzoate, have been shown to possess carcinogenic properties. This study investigated the cytotoxic effects of potassium benzoate, a common food additive, on HepG2 liver cancer cells and THLE2 non-tumorigenic liver cells. Using the Neutral Red assay, we observed a concentration-dependent decrease in cell viability for both cell lines, with HepG2 cells showing higher sensitivity. The IC50 values were determined to be 72.50 µg/mL for HepG2 cells and 645.7 µg/mL for THLE2 cells, indicating potassium benzoate's potential cytotoxicity on both malignant and non-malignant cells. Flow cytometry analysis revealed that potassium benzoate treatment induced G2/M phase arrest in HepG2 cells, with a significant increase in the proportion of cells in the G2/M phase from 12% to 43%. Gene expression analysis using qRT-PCR demonstrated upregulation of p53, Bax, and p21, while Bcl-2, cyclin B1, and CDK1 were downregulated. These findings suggest that potassium benzoate has a high potential for cytotoxicity and genotoxicity when used as a food preservative. This study contributes to the growing body of evidence on the potential health impacts of food additives and underscores the need for further research into their long-term effects on human health.

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