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Treatment of echinococcosis: albendazole and mebendazole – what else?
Open accessAbstract
The search for novel therapeutic options to cure alveolar echinococcosis (AE), due to the metacestode of Echinococcus multilocularis, is ongoing, and these developments could also have a profound impact on the treatment of cystic echinococcosis (CE), caused by the closely related Echinococcus granulosus s.l. Several options are being explored. A viable strategy for the identification of novel chemotherapeutically valuable compounds includes whole-organism drug screening, employing large-scale in vitro metacestode cultures and, upon identification of promising compounds, verification of drug efficacy in small laboratory animals. Clearly, the current focus is targeted towards broad-spectrum anti-parasitic or anti-cancer drugs and compound classes that are already marketed, or that are in development for other applications. The availability of comprehensive Echinococcus genome information and gene expression data, as well as significant progress on the molecular level, has now opened the door for a more targeted drug discovery approach, which allows exploitation of defined pathways and enzymes that are essential for the parasite. In addition, current in vitro and in vivo models that are used to assess drug efficacy should be optimized and complemented by methods that give more detailed information on the host-parasite interactions that occur during drug treatments. The key to success is to identify, target and exploit those parasite molecules that orchestrate activities essential to parasite survival.
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“PAIR plus pre- or post-operative mebendazole therapy brought about greater clinical and parasitological efficacy compared with surgery alone [168,181,182]”
From Albendazole and Mebendazole as Anti-Parasitic and Anti-Cancer Agents: an Update (2021) · cites this paper as [168]
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Cited by
Sorted by citations
Albendazole and Mebendazole as Anti-Parasitic and Anti-Cancer Agents: an Update
Chai, J.-Y., Jung, B.-K., & Hong, S.-J. (2021) · The Korean Journal of Parasitology · doi:10.3347/kjp.2021.59.3.189 · Cited by 286
Metadata
- Authors
- Hemphill, A., Stadelmann, B., Rufener, R., Spiliotis, M., Boubaker, G., Müller, J., Müller, N., Gorgas, D., & Gottstein, B.
- Affiliations
- University of Bern (CH)
- Corresponding author
- Hemphill, Andrew
- Venue
- Parasite
- Publisher
- EDP Sciences
- Published
- 2014
- Volume
- 21
- Pages
- 70
- ISSN
- 1252-607X (ISSN-L)
- 1776-1042
- PMC
- PMC4271654
- OpenAlex
- W2126447740
- Cited by
- 173
- References
- 0
- Citations by year
- 2026: 6 · 2025: 11 · 2024: 18 · 2023: 13 · 2022: 19 · 2021: 27 · 2020: 17 · 2019: 21 · 2018: 16 · 2017: 11 · 2016: 11 · 2015: 3
- FWCI
- 1.18
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by
- Locations
- Parasite (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Springer Link (Chiba Institute of Technology) (submittedVersion, other-oa)
- BORIS (University Library Bern) (submittedVersion, cc-by)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- National Science Foundation
- University of Bern
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (31,003A_141039/1, 141039)
- Gottfried und Julia Bangerter-Rhyner-Stiftung
- Topics
- Life Sciences › Immunology and Microbiology › Parasitology › Parasitic infections in humans and animals
- Life Sciences › Immunology and Microbiology › Parasitology › Helminth infection and control
- Life Sciences › Immunology and Microbiology › Parasitology › Parasites and Host Interactions
- Keywords
- echinococcosis, alveolar echinococcosis, Echinococcus multilocularis, Echinococcus granulosus, albendazole, mebendazole, anthelmintic drug discovery, host-parasite interactions, targeted drug discovery, parasite genome
- MeSH terms
- Animals, Anthelmintics, Cell Division, Drug Evaluation, Preclinical, Echinococcosis, Echinococcosis, Hepatic, Forecasting, Guanidines, Host-Parasite Interactions, Humans, Imidazoles, Larva, Mebendazole, Nitro Compounds, Thiazoles, Thiophenes, Drug Design, Albendazole, Mefloquine, Helminth Proteins, Clarithromycin, Echinococcus multilocularis, Mice, Cytostatic Agents, Molecular Targeted Therapy
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