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Published on: January 19, 2019
Fenbendazole as a potential anticancer drug
Qiwen Duan1, Yanfeng Liu, Sara Rockwell
1Department of Therapeutic Radiology, Yale University School of Medicine, PO Box 208040, New Haven, CT 06520-8040, USA. sara.rockwell@yale.edu
Background/Aims:
To evaluate the anticancer activity of fenbendazole, a widely used antihelminth with mechanisms of action that overlap with those of the hypoxia-selective nitroheterocyclic cytotoxins/radiosensitizers and the taxanes.
Materials And Methods:
We used EMT6 mouse mammary tumor cells in cell culture and as solid tumors in mice to examine the cytotoxic and antitumor effects of fenbendazole as a single agent and in combination regimens.
Results:
Intensive treatments with fenbendazole were toxic to EMT6 cells in vitro; toxicity increased with incubation time and under conditions of severe hypoxia. Fenbendazole did not alter the dose-response curves for radiation or docetaxel; instead, the agents produced additive cytotoxicities. Febendazole in maximally-intensive regimens did not alter the growth of EMT6 tumors, or increase the antineoplastic effects of radiation.
Conclusion:
These studies provided no evidence that fenbendazole would have value in cancer therapy, but suggested that this general class of compounds merits further investigation.
Insights
Fenbendazole, an antihelminth drug, showed no significant anticancer effects alone or with radiation and docetaxel in mouse models. Further investigation into this drug class is suggested for potential cancer therapy applications.
Area of Science:
- Pharmacology
- Oncology
- Drug Discovery
Background:
- Fenbendazole is a broad-spectrum antihelminth.
- Its mechanism of action shares similarities with hypoxia-selective cytotoxins and taxanes.
Purpose of the Study:
- To evaluate the anticancer activity of fenbendazole.
- To assess its efficacy as a single agent and in combination therapies.
Main Methods:
- In vitro studies using EMT6 mouse mammary tumor cells.
- In vivo studies using solid EMT6 tumors in mice.
- Combination treatments with radiation and docetaxel were investigated.
Main Results:
- Fenbendazole exhibited in vitro toxicity to EMT6 cells, enhanced by incubation time and severe hypoxia.
- No synergistic effects were observed when combined with radiation or docetaxel; additive toxicities were noted.
- Fenbendazole did not inhibit tumor growth or potentiate radiation's antineoplastic effects in vivo.
Conclusions:
- Current evidence does not support fenbendazole's use in cancer therapy.
- The broader class of compounds warrants further investigation for potential anticancer applications.
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