Oral Fenbendazole for Cancer Therapy in Humans and Animals

被引:0
作者
Nguyen, Jolie [1 ]
Nguyen, Thai q. [2 ]
Han, Bo [3 ]
Hoang, Ba x. [3 ]
机构
[1] Univ Pittsburgh, Sch Pharm, Pittsburgh, PA USA
[2] Univ Sci & Technol Hanoi, Life Sci Dept, Hanoi, Vietnam
[3] Univ Southern Calif, Keck Sch Med, Nimni Cordoba Tissue Engn & Drug Discovery Lab, Dept Surg, 1333 San Pablo St,BMT 302, Los Angeles, CA 90007 USA
关键词
Fenbendazole; fenbendazole pharmacokinetics; cancer treatment; repurposed drugs; glycolysis inhibitors; review; CELL LUNG-CANCER; METABOLIC REQUIREMENTS; ORGANIC-SOLVENTS; ALBENDAZOLE; MICROTUBULE; DISPOSITION; POTENT; MICE;
D O I
10.21873/anticanres.17197
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:3725 / 3735
页数:11
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