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Akt in the pathogenesis of COPD
In this review we consider the therapeutic potential of targeting Akt for the treatment of COPD. Akt is a serine/threonine protein kinase that functions as a signaling intermediate linked to multiple signaling programs involved in survival, inflammation, and growth. Akt is closely associated with ke...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2706607/ https://www.ncbi.nlm.nih.gov/pubmed/18046900 |
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author | Bozinovski, Steven Vlahos, Ross Hansen, Michelle Liu, Ken Anderson, Gary P |
author_facet | Bozinovski, Steven Vlahos, Ross Hansen, Michelle Liu, Ken Anderson, Gary P |
author_sort | Bozinovski, Steven |
collection | PubMed |
description | In this review we consider the therapeutic potential of targeting Akt for the treatment of COPD. Akt is a serine/threonine protein kinase that functions as a signaling intermediate linked to multiple signaling programs involved in survival, inflammation, and growth. Akt is closely associated with key membrane-bound receptors and represents a convergent integration point for multiple stimuli implicated in COPD pathogenesis. Persistent activation of Akt secondary to somatic mutations in regulatory oncogenes, such as PTEN, may explain why inflammation in COPD does not resolve when smoking is ceased. Akt is also implicated in the systemic manifestations of COPD such as skeletal muscle wasting and metabolic disturbances. Furthermore, targeting Akt may provide a useful means of limiting the severity and duration of disease exacerbations in COPD. As such, Akt represents a particularly attractive therapeutic target for the treatment of COPD. Interestingly, current knowledge suggests that both inhibitors and activators of Akt may be useful for treating different clinical subpopulations of COPD patients. |
format | Text |
id | pubmed-2706607 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-27066072009-07-27 Akt in the pathogenesis of COPD Bozinovski, Steven Vlahos, Ross Hansen, Michelle Liu, Ken Anderson, Gary P Int J Chron Obstruct Pulmon Dis Reviews In this review we consider the therapeutic potential of targeting Akt for the treatment of COPD. Akt is a serine/threonine protein kinase that functions as a signaling intermediate linked to multiple signaling programs involved in survival, inflammation, and growth. Akt is closely associated with key membrane-bound receptors and represents a convergent integration point for multiple stimuli implicated in COPD pathogenesis. Persistent activation of Akt secondary to somatic mutations in regulatory oncogenes, such as PTEN, may explain why inflammation in COPD does not resolve when smoking is ceased. Akt is also implicated in the systemic manifestations of COPD such as skeletal muscle wasting and metabolic disturbances. Furthermore, targeting Akt may provide a useful means of limiting the severity and duration of disease exacerbations in COPD. As such, Akt represents a particularly attractive therapeutic target for the treatment of COPD. Interestingly, current knowledge suggests that both inhibitors and activators of Akt may be useful for treating different clinical subpopulations of COPD patients. Dove Medical Press 2006-03 2006-03 /pmc/articles/PMC2706607/ /pubmed/18046900 Text en © 2006 Dove Medical Press Limited. All rights reserved |
spellingShingle | Reviews Bozinovski, Steven Vlahos, Ross Hansen, Michelle Liu, Ken Anderson, Gary P Akt in the pathogenesis of COPD |
title | Akt in the pathogenesis of COPD |
title_full | Akt in the pathogenesis of COPD |
title_fullStr | Akt in the pathogenesis of COPD |
title_full_unstemmed | Akt in the pathogenesis of COPD |
title_short | Akt in the pathogenesis of COPD |
title_sort | akt in the pathogenesis of copd |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2706607/ https://www.ncbi.nlm.nih.gov/pubmed/18046900 |
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