Repurposing antiplasmodial leads for cancer: Exploring the antiproliferative effects of N-cinnamoyl-aminoacridines

Bioorg Med Chem Lett. 2024 Oct 1:111:129894. doi: 10.1016/j.bmcl.2024.129894. Epub 2024 Jul 21.

Abstract

Drug repurposing and rescuing have been widely explored as cost-effective approaches to expand the portfolio of chemotherapeutic agents. Based on the reported antitumor properties of both trans-cinnamic acids and quinacrine, an antimalarial aminoacridine, we explored the antiproliferative properties of two series of N-cinnamoyl-aminoacridines recently identified as multi-stage antiplasmodial leads. The compounds were evaluated in vitro against three cancer cell lines (MKN-28, Huh-7, and HepG2), and human primary dermal fibroblasts. One of the series displayed highly selective antiproliferative activity in the micromolar range against the three cancer cell lines tested, without any toxicity to non-carcinogenic cells.

Keywords: Antitumor; Cancer; Covalent bitherapy; Hybrid; Malaria; Mepacrine; Recycling; Selectivity.

MeSH terms

  • Aminoacridines / chemical synthesis
  • Aminoacridines / chemistry
  • Aminoacridines / pharmacology
  • Antimalarials* / chemical synthesis
  • Antimalarials* / chemistry
  • Antimalarials* / pharmacology
  • Antineoplastic Agents* / chemical synthesis
  • Antineoplastic Agents* / chemistry
  • Antineoplastic Agents* / pharmacology
  • Cell Line, Tumor
  • Cell Proliferation* / drug effects
  • Cinnamates / chemical synthesis
  • Cinnamates / chemistry
  • Cinnamates / pharmacology
  • Dose-Response Relationship, Drug
  • Drug Repositioning
  • Drug Screening Assays, Antitumor*
  • Humans
  • Molecular Structure
  • Structure-Activity Relationship

Substances

  • Antineoplastic Agents
  • Antimalarials
  • Aminoacridines
  • Cinnamates