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Oral Fenbendazole for Cancer Therapy in Humans and Animals.
Nguyen, Jolie; Nguyen, Thai Q; Han, B O; Hoang, Ba X.
Affiliation
  • Nguyen J; School of Pharmacy, University of Pittsburgh, Pittsburgh, PA, U.S.A.
  • Nguyen TQ; Life Science Department, University of Science and Technology of Hanoi, Hanoi, Vietnam.
  • Han BO; Nimni-Cordoba Tissue Engineering and Drug Discovery Lab, Department of Surgery, Keck School of Medicine of University of Southern California, Los Angeles, CA, U.S.A.
  • Hoang BX; Nimni-Cordoba Tissue Engineering and Drug Discovery Lab, Department of Surgery, Keck School of Medicine of University of Southern California, Los Angeles, CA, U.S.A. baxuanho@usc.edu.
Anticancer Res ; 44(9): 3725-3735, 2024 Sep.
Article in En | MEDLINE | ID: mdl-39197912
ABSTRACT
Fenbendazole is a benzimidazole anthelmintic agent commonly used to treat animal parasitic infections. In humans, other benzimidazoles, such as mebendazole and albendazole, are used as antiparasitic agents. Since fenbendazole is not currently approved by the FDA or EMA, its pharmacokinetics and safety in humans have yet to be well-documented in medical literature. Despite this, insights can be drawn from existing in vitro and in vivo animal studies on its pharmacokinetics. Given the low cost of fenbendazole, its high safety profile, accessibility, and unique anti-proliferative activities, fenbendazole would be the preferred benzimidazole compound to treat cancer. To ensure patient safety in the repurposing use of fenbendazole, it is crucial to perform clinical trials to assess its potential anticancer effects, optimal doses, therapeutic regimen, and tolerance profiles. This review focuses on the pharmacokinetics of orally administered fenbendazole and its promising anticancer biological activities, such as inhibiting glycolysis, down-regulating glucose uptake, inducing oxidative stress, and enhancing apoptosis in published experimental studies. Additionally, we evaluated the toxicity profile of fenbendazole and discussed possibilities for improving the bioavailability of the drug, enhancing its efficacy, and reducing potential toxicity.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Fenbendazole / Neoplasms Limits: Animals / Humans Language: En Journal: Anticancer Res Year: 2024 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Fenbendazole / Neoplasms Limits: Animals / Humans Language: En Journal: Anticancer Res Year: 2024 Type: Article Affiliation country: United States