Imatinib Treatment Causes Substantial ...
Document type :
Article dans une revue scientifique
Permalink :
Title :
Imatinib Treatment Causes Substantial Transcriptional Changes in Adult Schistosoma mansoni In Vitro Exhibiting Pleiotropic Effects
Author(s) :
Buro, Christin [Auteur]
Justus-Liebig-Universität Gießen = Justus Liebig University [JLU]
Beckmann, Svenja [Auteur]
Justus-Liebig-Universität Gießen = Justus Liebig University [JLU]
Oliveira, Katia C. [Auteur]
Universidade de São Paulo = University of São Paulo [USP]
Dissous, Colette [Auteur]
Centre d’Infection et d’Immunité de Lille - INSERM U 1019 - UMR 9017 - UMR 8204 [CIIL]
Cailliau, Katia [Auteur]
Unité de Glycobiologie Structurale et Fonctionnelle - UMR 8576 [UGSF]
Marhöfer, Richard J. [Auteur]
Selzer, Paul M. [Auteur]
Verjovski-Almeida, Sergio [Auteur]
Universidade de São Paulo = University of São Paulo [USP]
Grevelding, Christoph G. [Auteur]
Justus-Liebig-Universität Gießen = Justus Liebig University [JLU]
Justus-Liebig-Universität Gießen = Justus Liebig University [JLU]
Beckmann, Svenja [Auteur]
Justus-Liebig-Universität Gießen = Justus Liebig University [JLU]
Oliveira, Katia C. [Auteur]
Universidade de São Paulo = University of São Paulo [USP]
Dissous, Colette [Auteur]

Centre d’Infection et d’Immunité de Lille - INSERM U 1019 - UMR 9017 - UMR 8204 [CIIL]
Cailliau, Katia [Auteur]

Unité de Glycobiologie Structurale et Fonctionnelle - UMR 8576 [UGSF]
Marhöfer, Richard J. [Auteur]
Selzer, Paul M. [Auteur]
Verjovski-Almeida, Sergio [Auteur]
Universidade de São Paulo = University of São Paulo [USP]
Grevelding, Christoph G. [Auteur]
Justus-Liebig-Universität Gießen = Justus Liebig University [JLU]
Journal title :
PLoS neglected tropical diseases
Volume number :
8
Pages :
e2923
Publication date :
2014-06-12
ISSN :
1935-2735
English keyword(s) :
Schistosoma
Microarrays
Schistosoma Mansoni
Muscle proteins
Eggs
Gene regulation
DNA transcription
Protein kinases
Microarrays
Schistosoma Mansoni
Muscle proteins
Eggs
Gene regulation
DNA transcription
Protein kinases
HAL domain(s) :
Chimie/Chimie théorique et/ou physique
English abstract : [en]
Background
Schistosome parasites cause schistosomiasis, one of the most important infectious diseases worldwide. For decades Praziquantel (PZQ) is the only drug widely used for controlling schistosomiasis. The absence of ...
Show more >Background Schistosome parasites cause schistosomiasis, one of the most important infectious diseases worldwide. For decades Praziquantel (PZQ) is the only drug widely used for controlling schistosomiasis. The absence of a vaccine and fear of PZQ resistance have motivated the search for alternatives. Studies on protein kinases (PKs) demonstrated their importance for diverse physiological processes in schistosomes. Among others two Abl tyrosine kinases, SmAbl1 and SmAbl2, were identified in Schistosoma mansoni and shown to be transcribed in the gonads and the gastrodermis. SmAbl1 activity was blocked by Imatinib, a known Abl-TK inhibitor used in human cancer therapy (Gleevec/Glivec). Imatinib exhibited dramatic effects on the morphology and physiology of adult schistosomes in vitro causing the death of the parasites. Methodology/Principal Findings Here we show modeling data supporting the targeting of SmAbl1/2 by Imatinib. A biochemical assay confirmed that SmAbl2 activity is also inhibited by Imatinib. Microarray analyses and qRT-PCR experiments were done to unravel transcriptional processes influenced by Imatinib in adult schistosomes in vitro demonstrating a wide influence on worm physiology. Surface-, muscle-, gut and gonad-associated processes were affected as evidenced by the differential transcription of e.g. the gynecophoral canal protein gene GCP, paramyosin, titin, hemoglobinase, and cathepsins. Furthermore, transcript levels of VAL-7 and egg formation-associated genes such as tyrosinase 1, p14, and fs800-like were affected as well as those of signaling genes including a ribosomal protein S6 kinase and a glutamate receptor. Finally, a comparative in silico analysis of the obtained microarray data sets and previous data analyzing the effect of a TGFβR1 inhibitor on transcription provided first evidence for an association of TGFβ and Abl kinase signaling. Among others GCP and egg formation-associated genes were identified as common targets. Conclusions/Significance The data affirm broad negative effects of Imatinib on worm physiology substantiating the role of PKs as interesting targets.Show less >
Show more >Background Schistosome parasites cause schistosomiasis, one of the most important infectious diseases worldwide. For decades Praziquantel (PZQ) is the only drug widely used for controlling schistosomiasis. The absence of a vaccine and fear of PZQ resistance have motivated the search for alternatives. Studies on protein kinases (PKs) demonstrated their importance for diverse physiological processes in schistosomes. Among others two Abl tyrosine kinases, SmAbl1 and SmAbl2, were identified in Schistosoma mansoni and shown to be transcribed in the gonads and the gastrodermis. SmAbl1 activity was blocked by Imatinib, a known Abl-TK inhibitor used in human cancer therapy (Gleevec/Glivec). Imatinib exhibited dramatic effects on the morphology and physiology of adult schistosomes in vitro causing the death of the parasites. Methodology/Principal Findings Here we show modeling data supporting the targeting of SmAbl1/2 by Imatinib. A biochemical assay confirmed that SmAbl2 activity is also inhibited by Imatinib. Microarray analyses and qRT-PCR experiments were done to unravel transcriptional processes influenced by Imatinib in adult schistosomes in vitro demonstrating a wide influence on worm physiology. Surface-, muscle-, gut and gonad-associated processes were affected as evidenced by the differential transcription of e.g. the gynecophoral canal protein gene GCP, paramyosin, titin, hemoglobinase, and cathepsins. Furthermore, transcript levels of VAL-7 and egg formation-associated genes such as tyrosinase 1, p14, and fs800-like were affected as well as those of signaling genes including a ribosomal protein S6 kinase and a glutamate receptor. Finally, a comparative in silico analysis of the obtained microarray data sets and previous data analyzing the effect of a TGFβR1 inhibitor on transcription provided first evidence for an association of TGFβ and Abl kinase signaling. Among others GCP and egg formation-associated genes were identified as common targets. Conclusions/Significance The data affirm broad negative effects of Imatinib on worm physiology substantiating the role of PKs as interesting targets.Show less >
Language :
Anglais
Audience :
Non spécifiée
Administrative institution(s) :
CNRS
Université de Lille
Université de Lille
Research team(s) :
Régulation des signaux de division
Submission date :
2020-02-12T15:44:32Z
2021-01-08T08:18:11Z
2021-06-04T12:34:10Z
2021-01-08T08:18:11Z
2021-06-04T12:34:10Z
Files
- pntd.0002923.pdf
- Version éditeur
- Open access
- Access the document