Literature DB >> 22607149

The redox biology of schistosome parasites and applications for drug development.

Hsin-Hung Huang1, Coraline Rigouin, David L Williams.   

Abstract

Schistosomiasis caused by Schistosoma spp. is a serious public health concern, especially in sub-Saharan Africa. Praziquantel is the only drug currently administrated to treat this disease. However, praziquantel-resistant parasites have been identified in endemic areas and can be generated in the laboratory. Therefore, it is essential to find new therapeutics. Antioxidants are appealing drug targets. In order to survive in their hosts, schistosomes are challenged by reactive oxygen species from intrinsic and extrinsic sources. Schistosome antioxidant enzymes have been identified as essential proteins and novel drug targets and inhibition of the antioxidant response can lead to parasite death. Because the organization of the redox network in schistosomes is significantly different from that in humans, new drugs are being developed targeting schistosome antioxidants. In this paper the redox biology of schistosomes is discussed and their potential use as drug targets is reviewed. It is hoped that compounds targeting parasite antioxidant responses will become clinically relevant drugs in the near future.

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Year:  2012        PMID: 22607149      PMCID: PMC3638776     

Source DB:  PubMed          Journal:  Curr Pharm Des        ISSN: 1381-6128            Impact factor:   3.116


  222 in total

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Journal:  Mol Biol Cell       Date:  2003-12-29       Impact factor: 4.138

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  10 in total

Review 1.  Bioorganometallic Compounds as Novel Drug Targets against Schistosomiasis in Sub-Saharan Africa: An alternative to Praziquantel?

Authors:  Cuma Cumisa Ndamse; Priscilla Masamba; Abidemi Paul Kappo
Journal:  Adv Pharm Bull       Date:  2021-05-30

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Review 3.  Immunological and Biochemical Interplay between Cytokines, Oxidative Stress and Schistosomiasis.

Authors:  Priscilla Masamba; Abidemi Paul Kappo
Journal:  Int J Mol Sci       Date:  2021-07-05       Impact factor: 5.923

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Journal:  Front Immunol       Date:  2015-06-02       Impact factor: 7.561

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Journal:  Int J Parasitol Drugs Drug Resist       Date:  2014-08-07       Impact factor: 4.077

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Authors:  Christian Stutzer; Sabine A Richards; Mariette Ferreira; Samantha Baron; Christine Maritz-Olivier
Journal:  Front Cell Infect Microbiol       Date:  2018-03-13       Impact factor: 5.293

7.  Towards an understanding of the function of the phytochelatin synthase of Schistosoma mansoni.

Authors:  Coraline Rigouin; Elyse Nylin; Alexis A Cogswell; Dirk Schaumlöffel; Dirk Dobritzsch; David L Williams
Journal:  PLoS Negl Trop Dis       Date:  2013-01-31

8.  High-throughput screening against thioredoxin glutathione reductase identifies novel inhibitors with potential therapeutic value for schistosomiasis.

Authors:  Ting Li; Peter D Ziniel; Pan-Qing He; Valerie P Kommer; Gregory J Crowther; Min He; Qing Liu; Wesley C Van Voorhis; David L Williams; Ming-Wei Wang
Journal:  Infect Dis Poverty       Date:  2015-08-31       Impact factor: 4.520

9.  The diterpenoid 7-keto-sempervirol, derived from Lycium chinense, displays anthelmintic activity against both Schistosoma mansoni and Fasciola hepatica.

Authors:  Jennifer Edwards; Martha Brown; Emily Peak; Barbara Bartholomew; Robert J Nash; Karl F Hoffmann
Journal:  PLoS Negl Trop Dis       Date:  2015-03-13

10.  Computationally-guided drug repurposing enables the discovery of kinase targets and inhibitors as new schistosomicidal agents.

Authors:  Sandra Giuliani; Arthur C Silva; Joyce V V B Borba; Pablo I P Ramos; Ross A Paveley; Eugene N Muratov; Carolina Horta Andrade; Nicholas Furnham
Journal:  PLoS Comput Biol       Date:  2018-10-22       Impact factor: 4.475

  10 in total

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