In vitro cytotoxic and molecular effects of metoprolol, alone or combined with cisplatin, on colon cancer cells

Authors

  • Teeb Ali Al-Saady
  • Ooroba M. S. Ibrahim
  • Hany Akeel Al-Hussaniy

DOI:

https://doi.org/10.60988/p.v37i2S.164

Keywords:

metoprolol; cisplatin; colon cancer cells; cell viability; cytotoxicity

Abstract

Colorectal cancer ranks among the most prevalent malignancies worldwide, with surgical interventions frequently associated with substantial postoperative mortality and complications. Contemporary therapies often target molecular pathways such as the epidermal growth factor receptor and vascular endothelial growth factor. Recently, antihypertensive agents have been investigated for their potential anticancer properties, though results remain inconclusive. This study has assessed the cytotoxic effects of metoprolol, both as a monotherapy and in combination with cisplatin, on the SW480 colon cancer cell line using the MTT assay. Cisplatin achieved the highest cytotoxic activity at a concentration of 62.5 µg/mL, while metoprolol alone exhibited maximal cell-killing effects at 1,000 µg/mL. Notably, the combination of metoprolol (1,000 µg/mL) with cisplatin (15.6 µg/mL) demonstrated the most pronounced cytotoxic effect, thereby indicating potential synergistic activity. The findings suggest the potential of repurposing metoprolol as an adjunctive agent in combination chemotherapy, in order to enhance therapeutic outcomes in colorectal cancer treatment.

Author Biographies

Teeb Ali Al-Saady

Department of Pharmacology, College of Pharmacy, University of Hilla, Hillah, Iraq

Ooroba M. S. Ibrahim

Department of Physiology, Biochemistry, and Pharmacology, College of Veterinary Medicine, University of Baghdad, Baghdad, Iraq

Hany Akeel Al-Hussaniy

Department of Pharmacology, College of Pharmacy, Al-Nisour University, Baghdad, Iraq

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Published

10-10-2025

How to Cite

[1]
Al-Saady, T.A. et al. 2025. In vitro cytotoxic and molecular effects of metoprolol, alone or combined with cisplatin, on colon cancer cells. Pharmakeftiki . 37, 2S (Oct. 2025). DOI:https://doi.org/10.60988/p.v37i2S.164.