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PAK Signaling in Oncogenesis
The p21-activated kinase (PAK) family of serine/threonine kinases plays a pivotal role in physiological processes including motility, survival, mitosis, transcription and translation. PAKs are evolutionally conserved and widely expressed in a variety of tissues and are often over expressed in multip...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2731678/ https://www.ncbi.nlm.nih.gov/pubmed/19465939 http://dx.doi.org/10.1038/onc.2009.119 |
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author | Molli, Poonam R. Li, Da-Qiang Brion, Murray Rayala, Suresh K. Kumar, Rakesh |
author_facet | Molli, Poonam R. Li, Da-Qiang Brion, Murray Rayala, Suresh K. Kumar, Rakesh |
author_sort | Molli, Poonam R. |
collection | PubMed |
description | The p21-activated kinase (PAK) family of serine/threonine kinases plays a pivotal role in physiological processes including motility, survival, mitosis, transcription and translation. PAKs are evolutionally conserved and widely expressed in a variety of tissues and are often over expressed in multiple cancer types. Depending on structural and functional similarities, the six members of PAK family are divided into two groups with three members in each group. Group I PAKs are activated by extracellular signals through GTPase-dependent and independent mechanisms. In contrast, group II PAKs are constitutively active. Over the years, accumulating data from tissue culture models and human tumors has increased our understanding about the biology of PAK family members. In this review, we have summarized the complex regulation of PAK and its downstream diverse myriads of effectors which in-turn are responsible for the biologic effects of PAK family of kinases in cancer cells. |
format | Text |
id | pubmed-2731678 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
record_format | MEDLINE/PubMed |
spelling | pubmed-27316782010-01-16 PAK Signaling in Oncogenesis Molli, Poonam R. Li, Da-Qiang Brion, Murray Rayala, Suresh K. Kumar, Rakesh Oncogene Article The p21-activated kinase (PAK) family of serine/threonine kinases plays a pivotal role in physiological processes including motility, survival, mitosis, transcription and translation. PAKs are evolutionally conserved and widely expressed in a variety of tissues and are often over expressed in multiple cancer types. Depending on structural and functional similarities, the six members of PAK family are divided into two groups with three members in each group. Group I PAKs are activated by extracellular signals through GTPase-dependent and independent mechanisms. In contrast, group II PAKs are constitutively active. Over the years, accumulating data from tissue culture models and human tumors has increased our understanding about the biology of PAK family members. In this review, we have summarized the complex regulation of PAK and its downstream diverse myriads of effectors which in-turn are responsible for the biologic effects of PAK family of kinases in cancer cells. 2009-05-25 2009-07-16 /pmc/articles/PMC2731678/ /pubmed/19465939 http://dx.doi.org/10.1038/onc.2009.119 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Molli, Poonam R. Li, Da-Qiang Brion, Murray Rayala, Suresh K. Kumar, Rakesh PAK Signaling in Oncogenesis |
title | PAK Signaling in Oncogenesis |
title_full | PAK Signaling in Oncogenesis |
title_fullStr | PAK Signaling in Oncogenesis |
title_full_unstemmed | PAK Signaling in Oncogenesis |
title_short | PAK Signaling in Oncogenesis |
title_sort | pak signaling in oncogenesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2731678/ https://www.ncbi.nlm.nih.gov/pubmed/19465939 http://dx.doi.org/10.1038/onc.2009.119 |
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