Source:http://linkedlifedata.com/resource/pubmed/id/16278681
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
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pubmed:dateCreated |
2006-3-2
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pubmed:abstractText |
p21-activated protein kinase 1 (Pak1) plays an important role in several cellular processes, including cytoskeleton reorganization, promotion of the cell survival, and the estrogen receptor (ER) signaling. Pak1 expression and activity is deregulated in a number of cancers. Pak1 is activated by a variety of physiological signals; however, less is known about the negative regulators of Pak1. Here, we report a negative regulator of Pak1. By performing a yeast two-hybrid screen of a mammary gland library, we identified cysteine-rich inhibitor of Pak1 (CRIPak) as a novel Pak1-interacting protein. We found that CRIPak is an intronless gene that localized to chromosome 4p16.3. It contains 13 zinc-finger domains and has three trypsin inhibitor-like, cysteine-rich domains and is widely expressed in a number of human cells and tissues. We further found that CRIPak interacted with Pak1 through the N-terminal regulatory domain and inhibited Pak1 kinase in both in vitro and in vivo assays. CRIPak inhibited Pak1-mediated LIM kinase activation and enhancement of ER transactivation. Conversely, selective inhibition of the endogenous CRIPak resulted in an increased Pak1 activity, and consequently, increased cytoskeleton remodeling and Pak1-mediated ER transactivation activity. The hormonal stimulation of cells enhanced CRIPak expression and promoted its colocalization with ER in the nuclear compartment. Our findings suggest that CRIPak is a novel negative regulator of the Pak1 and has a role in the modulation of Pak1-mediated ER transactivation in breast cancer cells.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/PAK1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Protein-Serine-Threonine Kinases,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Estrogen,
http://linkedlifedata.com/resource/pubmed/chemical/p21-Activated Kinases
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0950-9232
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
2
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pubmed:volume |
25
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1311-9
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:16278681-Amino Acid Sequence,
pubmed-meshheading:16278681-Animals,
pubmed-meshheading:16278681-Breast Neoplasms,
pubmed-meshheading:16278681-COS Cells,
pubmed-meshheading:16278681-Carrier Proteins,
pubmed-meshheading:16278681-Cercopithecus aethiops,
pubmed-meshheading:16278681-Chromosomes, Human, Pair 4,
pubmed-meshheading:16278681-Cytoskeleton,
pubmed-meshheading:16278681-Female,
pubmed-meshheading:16278681-Humans,
pubmed-meshheading:16278681-Molecular Sequence Data,
pubmed-meshheading:16278681-Protein-Serine-Threonine Kinases,
pubmed-meshheading:16278681-Receptors, Estrogen,
pubmed-meshheading:16278681-Signal Transduction,
pubmed-meshheading:16278681-Two-Hybrid System Techniques,
pubmed-meshheading:16278681-p21-Activated Kinases
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pubmed:year |
2006
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pubmed:articleTitle |
CRIPak, a novel endogenous Pak1 inhibitor.
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pubmed:affiliation |
Department of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
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pubmed:publicationType |
Journal Article,
Research Support, N.I.H., Extramural
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