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...

Full description

Bibliographic Details
Main Authors: John A. Marwick, Kian Fan Chung, Ian M. Adcock
Format: Article
Language:English
Published: SAGE Publishing 2010-02-01
Series:Therapeutic Advances in Respiratory Disease
Online Access:https://doi.org/10.1177/1753465809352792
id doaj-f83da90d111b4809b5109aeab8c6ae08
record_format Article
spelling 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
work_keys_str_mv AT johnamarwick phosphatidylinositol3kinaseisoformsastargetsinrespiratorydisease
AT kianfanchung phosphatidylinositol3kinaseisoformsastargetsinrespiratorydisease
AT ianmadcock phosphatidylinositol3kinaseisoformsastargetsinrespiratorydisease
_version_ 1724694860851576832