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Preclinical Activity of Eltrombopag (SB-497115), an Oral, Nonpeptide Thrombopoietin Receptor Agonist

Eltrombopag is a first-in-class, orally bioavailable, small-molecule, nonpeptide agonist of the thrombopoietin receptor (TpoR), which is being developed as a treatment for thrombocytopenia of various etiologies. In vitro studies have demonstrated that the activity of eltrombopag is dependent on expr...

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Autores principales: Erickson-Miller, Connie L, Delorme, Evelyne, Tian, Shin-Shay, Hopson, Christopher B, Landis, Amy J, Valoret, Elizabeth I, Sellers, Teresa S, Rosen, Jon, Miller, Stephen G, Luengo, Juan I, Duffy, Kevin J, Jenkins, Julian M
Formato: Texto
Lenguaje:English
Publicado: Wiley Subscription Services, Inc., A Wiley Company 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2729672/
https://www.ncbi.nlm.nih.gov/pubmed/19038790
http://dx.doi.org/10.1634/stemcells.2008-0366
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author Erickson-Miller, Connie L
Delorme, Evelyne
Tian, Shin-Shay
Hopson, Christopher B
Landis, Amy J
Valoret, Elizabeth I
Sellers, Teresa S
Rosen, Jon
Miller, Stephen G
Luengo, Juan I
Duffy, Kevin J
Jenkins, Julian M
author_facet Erickson-Miller, Connie L
Delorme, Evelyne
Tian, Shin-Shay
Hopson, Christopher B
Landis, Amy J
Valoret, Elizabeth I
Sellers, Teresa S
Rosen, Jon
Miller, Stephen G
Luengo, Juan I
Duffy, Kevin J
Jenkins, Julian M
author_sort Erickson-Miller, Connie L
collection PubMed
description Eltrombopag is a first-in-class, orally bioavailable, small-molecule, nonpeptide agonist of the thrombopoietin receptor (TpoR), which is being developed as a treatment for thrombocytopenia of various etiologies. In vitro studies have demonstrated that the activity of eltrombopag is dependent on expression of TpoR, which activates the signaling transducers and activators of transcription (STAT) and mitogen-activated protein kinase signal transduction pathways. The objective of this preclinical study is to determine if eltrombopag interacts selectively with the TpoR to facilitate megakaryocyte differentiation in platelets. Functional thrombopoietic activity was demonstrated by the proliferation and differentiation of primary human CD34(+) bone marrow cells into CD41(+) megakaryocytes. Measurements in platelets in several species indicated that eltrombopag specifically activates only the human and chimpanzee STAT pathways. The in vivo activity of eltrombopag was demonstrated by an increase of up to 100% in platelet numbers when administered orally (10 mg/kg per day for 5 days) to chimpanzees. In conclusion, eltrombopag interacts selectively with the TpoR without competing with Tpo, leading to the increased proliferation and differentiation of human bone marrow progenitor cells into megakaryocytes and increased platelet production. These results suggest that eltrombopag and Tpo may be able to act additively to increase platelet production.
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spelling pubmed-27296722009-08-27 Preclinical Activity of Eltrombopag (SB-497115), an Oral, Nonpeptide Thrombopoietin Receptor Agonist Erickson-Miller, Connie L Delorme, Evelyne Tian, Shin-Shay Hopson, Christopher B Landis, Amy J Valoret, Elizabeth I Sellers, Teresa S Rosen, Jon Miller, Stephen G Luengo, Juan I Duffy, Kevin J Jenkins, Julian M Stem Cells Original Article Eltrombopag is a first-in-class, orally bioavailable, small-molecule, nonpeptide agonist of the thrombopoietin receptor (TpoR), which is being developed as a treatment for thrombocytopenia of various etiologies. In vitro studies have demonstrated that the activity of eltrombopag is dependent on expression of TpoR, which activates the signaling transducers and activators of transcription (STAT) and mitogen-activated protein kinase signal transduction pathways. The objective of this preclinical study is to determine if eltrombopag interacts selectively with the TpoR to facilitate megakaryocyte differentiation in platelets. Functional thrombopoietic activity was demonstrated by the proliferation and differentiation of primary human CD34(+) bone marrow cells into CD41(+) megakaryocytes. Measurements in platelets in several species indicated that eltrombopag specifically activates only the human and chimpanzee STAT pathways. The in vivo activity of eltrombopag was demonstrated by an increase of up to 100% in platelet numbers when administered orally (10 mg/kg per day for 5 days) to chimpanzees. In conclusion, eltrombopag interacts selectively with the TpoR without competing with Tpo, leading to the increased proliferation and differentiation of human bone marrow progenitor cells into megakaryocytes and increased platelet production. These results suggest that eltrombopag and Tpo may be able to act additively to increase platelet production. Wiley Subscription Services, Inc., A Wiley Company 2009-02 /pmc/articles/PMC2729672/ /pubmed/19038790 http://dx.doi.org/10.1634/stemcells.2008-0366 Text en Copyright © 2009 AlphaMed Press http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Original Article
Erickson-Miller, Connie L
Delorme, Evelyne
Tian, Shin-Shay
Hopson, Christopher B
Landis, Amy J
Valoret, Elizabeth I
Sellers, Teresa S
Rosen, Jon
Miller, Stephen G
Luengo, Juan I
Duffy, Kevin J
Jenkins, Julian M
Preclinical Activity of Eltrombopag (SB-497115), an Oral, Nonpeptide Thrombopoietin Receptor Agonist
title Preclinical Activity of Eltrombopag (SB-497115), an Oral, Nonpeptide Thrombopoietin Receptor Agonist
title_full Preclinical Activity of Eltrombopag (SB-497115), an Oral, Nonpeptide Thrombopoietin Receptor Agonist
title_fullStr Preclinical Activity of Eltrombopag (SB-497115), an Oral, Nonpeptide Thrombopoietin Receptor Agonist
title_full_unstemmed Preclinical Activity of Eltrombopag (SB-497115), an Oral, Nonpeptide Thrombopoietin Receptor Agonist
title_short Preclinical Activity of Eltrombopag (SB-497115), an Oral, Nonpeptide Thrombopoietin Receptor Agonist
title_sort preclinical activity of eltrombopag (sb-497115), an oral, nonpeptide thrombopoietin receptor agonist
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2729672/
https://www.ncbi.nlm.nih.gov/pubmed/19038790
http://dx.doi.org/10.1634/stemcells.2008-0366
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