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CDC42 — RELA
Pathways - manually collected, often from reviews:
-
OpenBEL Selventa BEL large corpus:
RELA
→
CDC42
(increases, CDC42 Activity, RELA Activity)
Evidence: Fibronectin-induced p65 nuclear translocation was inhibited by the expression of dominant negative Cdc42 in HUVECs but the effect was smaller than that exerted by Rac.
Text-mined interactions from Literome
Huttunen et al., J Biol Chem 1999
(Neuroblastoma) :
In contrast, the activation of
NF-kappaB is
inhibited by dominant negative Ras but not Rac or
Cdc42
Puls et al., J Cell Sci 1999
(Inflammation) :
When expressed in fibroblasts, LMP1 stimulates
Cdc42 dependent filopodia formation as well as JNK and
NF(kappa)B activation
Cammarano et al., J Biol Chem 2001
:
Here we show that although Dbl activation of
NF kappa B requires
Cdc42 , Rac, and Rho, the different GTPases activate NF kappa B by different mechanisms ... Whereas Rac stimulates the activity of the I kappa B kinase IKK beta,
Cdc42 and Rho
activate NF kappa B without activating either IKK alpha or IKK beta
Zhao et al., Biochem J 2002
:
We also demonstrate that SP rapidly activates RhoA, Rac1 and
Cdc42 and that co-expression of the dominant negative mutants of RhoA, Rac1 and Cdc42 in NK-1R cDNA transfected NCM460 cells significantly
inhibits SP-induced
NF-kappaB dependent gene expression
Grassl et al., Cell Microbiol 2003
(MAP Kinase Signaling System) :
Using Clostridium difficile toxins that specifically inactivate small GTPases, and transfection of inhibitory proteins of the Rho-GTPases, we demonstrate that Rac1, but not
Cdc42 or Rho, is
required for activation of
NF-kappaB by invasin
Chen et al., Biochem Biophys Res Commun 2004
:
These results indicate that fMLP stimulates three members of the Rho family of GTPases Rac1, Cdc42, and RhoA activity in monocytes, and that Rac1 and RhoA, but not
Cdc42 , is
required for fMLP induced
NF-kappaB activation
Perona et al., Genes Dev 1997
:
The human RhoA,
CDC42 , and Rac-1 proteins efficiently
induce the transcriptional activity of
nuclear factor kappaB (NF-kappaB) by a mechanism that involves phosphorylation of Ikappa Balpha and translocation of p50/p50 and p50/p65 dimers to the nucleus, but independent of the Ras GTPase and the Raf-1 kinase ... In contrast, activation of
NF-kappaB by UV light was not
affected by Rho,
CDC42 , or Rac-1 dominant negative mutants
Montaner et al., J Biol Chem 1998
:
Finally, mutants of RhoA and
Cdc42Hs , but not that of Rac1,
inhibited the activation of
NF-kappaB by Ost