Literature DB >> 9560242

A role for Pak protein kinases in Schwann cell transformation.

Y Tang1, S Marwaha, J L Rutkowski, G I Tennekoon, P C Phillips, J Field.   

Abstract

Neurofibromatosis type 1 (NF1), a common autosomal dominant disorder caused by loss of the NF1 gene, is characterized clinically by neurofibromas and more rarely by neurofibrosarcomas. Neurofibromin, the protein encoded by NF1, possesses an intrinsic GTPase accelerating activity for the Ras proto-oncogene. Through this activity, it is a negative regulator of Ras. The Pak protein kinase is a candidate for a downstream signaling protein that may mediate Ras signals because it is activated by Rac and Cdc42, two small G proteins required for Ras signaling. Here, we use Pak mutants to explore the role of Pak in Ras signaling in Schwann cells, the cells affected in NF1. Whereas an activated Pak mutant does not transform cells, dominant negative Pak mutants are potent inhibitors of Ras transformation of rat Schwann cells and of a neurofibrosarcoma cell line from an NF1 patient. Although activated Pak stimulated jun-N-terminal kinase, inhibition of Ras transformation by dominant negative Pak did not require inhibition of jun-N-terminal kinase. Instead, the Pak mutants appeared to inhibit transformation by preventing Ras activation of the ERK/mitogen-activated protein kinase cascade. These results have implications for our understanding of NF1 because a neurofibrosarcoma cell line derived from a patient with NF1 was reverted by stable expression of the Pak dominant negative mutants.

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Year:  1998        PMID: 9560242      PMCID: PMC20227          DOI: 10.1073/pnas.95.9.5139

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  37 in total

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Journal:  Cell       Date:  1995-01-27       Impact factor: 41.582

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  27 in total

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Review 2.  P21 activated kinases: structure, regulation, and functions.

Authors:  Chetan K Rane; Audrey Minden
Journal:  Small GTPases       Date:  2014-03-21

Review 3.  Cdc42 in oncogenic transformation, invasion, and tumorigenesis.

Authors:  Kristy Stengel; Yi Zheng
Journal:  Cell Signal       Date:  2011-04-16       Impact factor: 4.315

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Authors:  J Qu; M S Cammarano; Q Shi; K C Ha; P de Lanerolle; A Minden
Journal:  Mol Cell Biol       Date:  2001-05       Impact factor: 4.272

5.  Fragile x mental retardation 1 and filamin a interact genetically in Drosophila long-term memory.

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Journal:  Front Neural Circuits       Date:  2010-01-08       Impact factor: 3.492

6.  p21-Activated kinases are required for transformation in a cell-based model of neurofibromatosis type 2.

Authors:  Hoi Yee Chow; Dina Stepanova; Jennifer Koch; Jonathan Chernoff
Journal:  PLoS One       Date:  2010-11-02       Impact factor: 3.240

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Authors:  Silvia Licciulli; Jasna Maksimoska; Chun Zhou; Scott Troutman; Smitha Kota; Qin Liu; Sergio Duron; David Campbell; Jonathan Chernoff; Jeffrey Field; Ronen Marmorstein; Joseph L Kissil
Journal:  J Biol Chem       Date:  2013-08-19       Impact factor: 5.157

9.  Induction of apoptosis in neurofibromatosis type 1 malignant peripheral nerve sheath tumor cell lines by a combination of novel farnesyl transferase inhibitors and lovastatin.

Authors:  Jonathan W Wojtkowiak; Farid Fouad; Daniel T LaLonde; Miriam D Kleinman; Richard A Gibbs; John J Reiners; Richard F Borch; Raymond R Mattingly
Journal:  J Pharmacol Exp Ther       Date:  2008-03-26       Impact factor: 4.030

10.  p21-Activated kinase 1 is required for efficient tumor formation and progression in a Ras-mediated skin cancer model.

Authors:  Hoi Yee Chow; Adrian M Jubb; Jennifer N Koch; Zahara M Jaffer; Dina Stepanova; David A Campbell; Sergio G Duron; Marie O'Farrell; Kathy Q Cai; Andres J P Klein-Szanto; J Silvio Gutkind; Klaus P Hoeflich; Jonathan Chernoff
Journal:  Cancer Res       Date:  2012-09-14       Impact factor: 12.701

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