scholarly journals CORRELATION BETWEEN THE EXPRESSION ACTIVITY OF ATYPICAL PROTEIN KINASE C ISOFORMS WITH METHYLATION OF THE MGMT GENE PROMOTER AND CO-DELETION OF 1P/19Q IN DIFFUSE GLIOMAS

2020 ◽  
pp. 40-44
Author(s):  
P.V. Nikitin ◽  
M.V. Ryzhova ◽  
S.A. Galstyan ◽  
E.A. Khokhlova
Keyword(s):  
Protein Kinase C ◽  
Protein Kinase ◽  
Gene Promoter ◽  
Atypical Protein Kinase C ◽  
Atypical Protein Kinase ◽  
Mgmt Gene ◽  
Kinase C ◽  
Diffuse Gliomas ◽  
Expression Activity ◽  
Protein Kinase C Isoforms

scholarly journals 663 Differential roles of atypical protein kinase C isoforms in wound healing

2017 ◽  
Vol 137 (10) ◽  
pp. S306
Author(s):  
S. Osada ◽  
N. Noguchi ◽  
T. Hirose ◽  
T. Suzuki ◽  
M. Kagaya ◽  
...  
Keyword(s):  
Wound Healing ◽  
Protein Kinase C ◽  
Protein Kinase ◽  
Atypical Protein Kinase C ◽  
Atypical Protein Kinase ◽  
Kinase C ◽  
Protein Kinase C Isoforms

An Allosteric Inhibitor Scaffold Targeting the PIF-Pocket of Atypical Protein Kinase C Isoforms

2017 ◽  
Vol 12 (2) ◽  
pp. 564-573 ◽  
Author(s):  
Jose M. Arencibia ◽  
Wolfgang Fröhner ◽  
Magdalena Krupa ◽  
Daniel Pastor-Flores ◽  
Piotr Merker ◽  
...  
Keyword(s):  
Protein Kinase C ◽  
Protein Kinase ◽  
Atypical Protein Kinase C ◽  
Atypical Protein Kinase ◽  
Allosteric Inhibitor ◽  
Kinase C ◽  
Protein Kinase C Isoforms

scholarly journals MEK5, a New Target of the Atypical Protein Kinase C Isoforms in Mitogenic Signaling

2001 ◽  
Vol 21 (4) ◽  
pp. 1218-1227 ◽  
Author(s):  
Marı́a T. Diaz-Meco ◽  
Jorge Moscat
Keyword(s):  
Protein Kinase C ◽  
Protein Kinase ◽  
Mitogen Activated Protein Kinase ◽  
Mitogenic Signaling ◽  
Atypical Protein Kinase C ◽  
Interaction Domain ◽  
Atypical Protein Kinase ◽  
Kinase C ◽  
Mitogen Activated Protein ◽  
Protein Kinase C Isoforms

ABSTRACT The MEK5–extracellular signal-regulated kinase (ERK5) tandem is a novel mitogen-activated protein kinase cassette critically involved in mitogenic activation by the epidermal growth factor (EGF). The atypical protein kinase C isoforms (aPKCs) have been shown to be required for cell growth and proliferation and have been reported to interact with the adapter protein p62 through a short stretch of acidic amino acids termed the aPKC interaction domain. This region is also present in MEK5, suggesting that it may be an aPKC-binding partner. Here we demonstrate that the aPKCs interact in an EGF-inducible manner with MEK5 and that this interaction is required and sufficient for the activation of MEK5 in response to EGF. Consistent with the role of the aPKCs in the MEK5-ERK5 pathway, we show that ζPKC and λ/ιPKC activate the Jun promoter through the MEF2C element, a well-established target of ERK5. From all these results, we conclude that MEK5 is a critical target of the aPKCs during mitogenic signaling.

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