Albendazole as a promising molecule for tumor control

L S E P W Castro1, M R Kviecinski2, F Ourique1

  • 1Department of Biochemistry, Universidade Federal de Santa Catarina (UFSC), Florianópolis, SC, Brazil.

Redox Biology
|October 7, 2016
PubMed

Insights

Albendazole (ABZ) shows antitumor effects by causing DNA damage and oxidative stress. This drug inhibits cancer cell growth and prolongs survival, suggesting its potential for new cancer treatments.

Area of Science:

  • Pharmacology
  • Molecular Biology
  • Cancer Research

Background:

  • Albendazole (ABZ) is an antiparasitic drug.
  • Its potential antitumor effects warrant investigation.
  • Understanding its mechanism of action is crucial for drug development.

Purpose of the Study:

  • To evaluate the antitumor effects of albendazole (ABZ).
  • To investigate the relationship between ABZ, oxidative stress, and DNA damage.
  • To explore ABZ as a potential lead molecule for novel anticancer drugs.

Main Methods:

  • In vitro studies using MCF-7 cells to assess cytotoxicity, colony formation, and reactive oxygen species (ROS) generation.
  • In vivo studies using Ehrlich carcinoma model in animals.
  • Analysis of DNA damage markers, oxidative stress biomarkers, and apoptosis-related proteins.

Main Results:

  • ABZ induced oxidative cleavage of DNA and decreased MCF-7 cell viability.
  • ABZ treatment increased intracellular ROS levels and inhibited cancer cell colony formation.
  • In vivo, ABZ inhibited tumor growth and prolonged survival, associated with oxidative stress and DNA damage induction.
  • NAC, an antioxidant, reversed ABZ-induced cytotoxicity and ROS generation.
  • ABZ triggered apoptosis signaling pathways, evidenced by altered protein expression and histone modification.

Conclusions:

  • Albendazole exhibits significant antitumor activity through induction of oxidative stress and DNA fragmentation.
  • ABZ promotes cancer cell death via apoptosis.
  • The findings highlight ABZ as a promising candidate for the development of new anticancer therapeutics.

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