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Related Concept Videos

Anthelminthic Agents01:15

Anthelminthic Agents

Anthelmintic drugs differ significantly from antiparasitic therapies targeting protozoa, primarily due to differences in parasite biology. Whereas most protozoal treatments act on proliferating cells, anthelmintics are typically directed against mature, nonproliferative helminths. The therapeutic approach considers the helminth's reliance on neuromuscular coordination, glucose metabolism, and microtubular integrity for survival, reproduction, and localization within the host. Most anthelmintics...
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Drugs that Destabilize Microtubules

Microtubules are dynamic structures and can be regulated by microtubule targeting agents (MTAs). Microtubule destabilizing drugs are a class of MTAs that destabilize and prevent microtubules' polymerization. Both natural and synthetic chemicals can be found under this class of drugs. Vincristine and vinblastine, two vinca alkaloids, and colchicine were among the first to be discovered. These drugs can affect cells in various ways, either by inducing a change in cell morphology, preventing...
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Drugs that Stabilize Microtubules

Microtubules are dynamic structures that undergo cycles of catastrophe and rescue. The microtubules play a central role in cell division by forming the spindle apparatus for segregating the chromosomes. This makes them ideal targets for regulating dividing cells in tumors and malignant cancer cells. Microtubule stabilizing drugs help stabilize the microtubule formation and promote its polymerization. Paclitaxel was the first microtubule stabilizing agent used as anticancer drug in chemotherapy...
Targeted Cancer Therapies02:57

Targeted Cancer Therapies

The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
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Combination Therapies and Personalized Medicine

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Mitogens and the Cell Cycle

Mitogens and their receptors play a crucial role in controlling the progression of the cell cycle. However, the loss of mitogenic control over cell division leads to tumor formation. Therefore, mitogens and mitogen receptors play an important role in cancer research. For instance, the epidermal growth factor (EGF) - a type of mitogen and its transmembrane receptor (EGFR), decides the fate of the cell's proliferation. When EGF binds to EGFR, a member of the ErbB family of tyrosine kinase...

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Potentiation of Anticancer Antibody Efficacy by Antineoplastic Drugs: Detection of Antibody-drug Synergism Using the Combination Index Equation
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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

Anticancer Research
|February 9, 2013
PubMed
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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.

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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.