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The Therapeutic Potential for PI3K Inhibitors in Autoimmune Rheumatic Diseases

The class 1 PI3Ks are lipid kinases with key roles in cell surface receptor-triggered signal transduction pathways. Two isoforms of the catalytic subunits, p110γ and p110δ, are enriched in leucocytes in which they promote activation, cellular growth, proliferation, differentiation and survival throu...

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Detalles Bibliográficos
Autores principales: Banham-Hall, Edward, Clatworthy, Menna R, Okkenhaug, Klaus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Open 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3460535/
https://www.ncbi.nlm.nih.gov/pubmed/23028409
http://dx.doi.org/10.2174/1874312901206010245
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author Banham-Hall, Edward
Clatworthy, Menna R
Okkenhaug, Klaus
author_facet Banham-Hall, Edward
Clatworthy, Menna R
Okkenhaug, Klaus
author_sort Banham-Hall, Edward
collection PubMed
description The class 1 PI3Ks are lipid kinases with key roles in cell surface receptor-triggered signal transduction pathways. Two isoforms of the catalytic subunits, p110γ and p110δ, are enriched in leucocytes in which they promote activation, cellular growth, proliferation, differentiation and survival through the generation of the second messenger PIP3. Genetic inactivation or pharmaceutical inhibition of these PI3K isoforms in mice result in impaired immune responses and reduced susceptibility to autoimmune and inflammatory conditions. We review the PI3K signal transduction pathways and the effects of inhibition of p110γ and/or p110δ on innate and adaptive immunity. Focusing on rheumatoid arthritis and systemic lupus erythematosus we discuss the preclinical evidence and prospects for small molecule inhibitors of p110γ and/or p110δ in autoimmune disease.
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spelling pubmed-34605352012-10-01 The Therapeutic Potential for PI3K Inhibitors in Autoimmune Rheumatic Diseases Banham-Hall, Edward Clatworthy, Menna R Okkenhaug, Klaus Open Rheumatol J Article The class 1 PI3Ks are lipid kinases with key roles in cell surface receptor-triggered signal transduction pathways. Two isoforms of the catalytic subunits, p110γ and p110δ, are enriched in leucocytes in which they promote activation, cellular growth, proliferation, differentiation and survival through the generation of the second messenger PIP3. Genetic inactivation or pharmaceutical inhibition of these PI3K isoforms in mice result in impaired immune responses and reduced susceptibility to autoimmune and inflammatory conditions. We review the PI3K signal transduction pathways and the effects of inhibition of p110γ and/or p110δ on innate and adaptive immunity. Focusing on rheumatoid arthritis and systemic lupus erythematosus we discuss the preclinical evidence and prospects for small molecule inhibitors of p110γ and/or p110δ in autoimmune disease. Bentham Open 2012-09-07 /pmc/articles/PMC3460535/ /pubmed/23028409 http://dx.doi.org/10.2174/1874312901206010245 Text en © Banham-Hall et al.; Licensee Bentham Open. http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Article
Banham-Hall, Edward
Clatworthy, Menna R
Okkenhaug, Klaus
The Therapeutic Potential for PI3K Inhibitors in Autoimmune Rheumatic Diseases
title The Therapeutic Potential for PI3K Inhibitors in Autoimmune Rheumatic Diseases
title_full The Therapeutic Potential for PI3K Inhibitors in Autoimmune Rheumatic Diseases
title_fullStr The Therapeutic Potential for PI3K Inhibitors in Autoimmune Rheumatic Diseases
title_full_unstemmed The Therapeutic Potential for PI3K Inhibitors in Autoimmune Rheumatic Diseases
title_short The Therapeutic Potential for PI3K Inhibitors in Autoimmune Rheumatic Diseases
title_sort therapeutic potential for pi3k inhibitors in autoimmune rheumatic diseases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3460535/
https://www.ncbi.nlm.nih.gov/pubmed/23028409
http://dx.doi.org/10.2174/1874312901206010245
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