Phosphatidylinositol 3-kinase isoforms as targets in respiratory disease
Respiratory diseases such as chronic obstructive pulmonary disease [COPD], severe asthma, cystic fibrosis [CF] and idiopathic pulmonary fibrosis [IPF] are inadequately controlled by current therapies. The underlying molecular mechanisms and pathogenesis of these diseases remain unclear, making ident...
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Series: | Therapeutic Advances in Respiratory Disease |
Online Access: | https://doi.org/10.1177/1753465809352792 |
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doaj-f83da90d111b4809b5109aeab8c6ae082020-11-25T03:01:07ZengSAGE PublishingTherapeutic Advances in Respiratory Disease1753-46582010-02-01410.1177/1753465809352792Phosphatidylinositol 3-kinase isoforms as targets in respiratory diseaseJohn A. Marwick Kian Fan ChungIan M. AdcockRespiratory diseases such as chronic obstructive pulmonary disease [COPD], severe asthma, cystic fibrosis [CF] and idiopathic pulmonary fibrosis [IPF] are inadequately controlled by current therapies. The underlying molecular mechanisms and pathogenesis of these diseases remain unclear, making identification and validation of potential new therapeutic targets difficult. However, recent studies have identified the central signalling mediator PI3K as playing an integral role in the immune system including initiation and maintenance of inflammatory responses. Specifically, the relatively leukocyte-specific PI3Kγ and PI3Kδ isoforms are central to leukocyte function and can be targeted pharmacologically. Early to man studies using selective PI3K isoform inhibitors are required to determine whether they have a future in treating respiratory disease, particularly in controlling both innate and adaptive inflammatory responses as well as restoring glucocorticoid function and reducing tumorigenesis.https://doi.org/10.1177/1753465809352792 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
John A. Marwick Kian Fan Chung Ian M. Adcock |
spellingShingle |
John A. Marwick Kian Fan Chung Ian M. Adcock Phosphatidylinositol 3-kinase isoforms as targets in respiratory disease Therapeutic Advances in Respiratory Disease |
author_facet |
John A. Marwick Kian Fan Chung Ian M. Adcock |
author_sort |
John A. Marwick |
title |
Phosphatidylinositol 3-kinase isoforms as targets in respiratory disease |
title_short |
Phosphatidylinositol 3-kinase isoforms as targets in respiratory disease |
title_full |
Phosphatidylinositol 3-kinase isoforms as targets in respiratory disease |
title_fullStr |
Phosphatidylinositol 3-kinase isoforms as targets in respiratory disease |
title_full_unstemmed |
Phosphatidylinositol 3-kinase isoforms as targets in respiratory disease |
title_sort |
phosphatidylinositol 3-kinase isoforms as targets in respiratory disease |
publisher |
SAGE Publishing |
series |
Therapeutic Advances in Respiratory Disease |
issn |
1753-4658 |
publishDate |
2010-02-01 |
description |
Respiratory diseases such as chronic obstructive pulmonary disease [COPD], severe asthma, cystic fibrosis [CF] and idiopathic pulmonary fibrosis [IPF] are inadequately controlled by current therapies. The underlying molecular mechanisms and pathogenesis of these diseases remain unclear, making identification and validation of potential new therapeutic targets difficult. However, recent studies have identified the central signalling mediator PI3K as playing an integral role in the immune system including initiation and maintenance of inflammatory responses. Specifically, the relatively leukocyte-specific PI3Kγ and PI3Kδ isoforms are central to leukocyte function and can be targeted pharmacologically. Early to man studies using selective PI3K isoform inhibitors are required to determine whether they have a future in treating respiratory disease, particularly in controlling both innate and adaptive inflammatory responses as well as restoring glucocorticoid function and reducing tumorigenesis. |
url |
https://doi.org/10.1177/1753465809352792 |
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