Affiliations 

  • 1 Department of Pharmacology, Jamia Hamdard, New Delhi, India
  • 2 Department of Biomedical Engineering, Indian Institute of Technology Ropar, Rupnagar, Punjab, India
  • 3 Department of Pharmacology and Toxicology, National Institute of Pharmaceutical Education and Research, Ahmedabad, Gujarat, India
  • 4 Biotechnology Institute, Ankara University, Ankara, Turkey
  • 5 School of Pharmacy, Monash University Malaysia, Jalan lagoon selatan, Petaling Jaya, Selangor, DE, Malaysia. nafees.Ahemad@monash.edu
  • 6 Department of Pharmacology and Toxicology, College of Pharmacy, University of Hail, Hail, Saudi Arabia. si.anwar@uoh.edu.sa
Mol Biol Rep, 2023 Sep;50(9):7667-7680.
PMID: 37418080 DOI: 10.1007/s11033-023-08568-1

Abstract

Antiepileptic drugs are versatile drugs with the potential to be used in functional drug formulations with drug repurposing approaches. In the present review, we investigated the anticancer properties of antiepileptic drugs and interlinked cancer and epileptic pathways. Our focus was primarily on those drugs that have entered clinical trials with positive results and those that provided good results in preclinical studies. Many contributing factors make cancer therapy fail, like drug resistance, tumor heterogeneity, and cost; exploring all alternatives for efficient treatment is important. It is crucial to find new drug targets to find out new antitumor molecules from the already clinically validated and approved drugs utilizing drug repurposing methods. The advancements in genomics, proteomics, and other computational approaches speed up drug repurposing. This review summarizes the potential of antiepileptic drugs in different cancers and tumor progression in the brain. Valproic acid, oxcarbazepine, lacosamide, lamotrigine, and levetiracetam are the drugs that showed potential beneficial outcomes against different cancers. Antiepileptic drugs might be a good option for adjuvant cancer therapy, but there is a need to investigate further their efficacy in cancer therapy clinical trials.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.