Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: EC:2.7.11.12 (
PKG
)
2,515
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Nitric oxide (NO) may activate soluble guanylyl cyclase (sGC), resulting in the increase of intracellular cyclic guanosine monophosphate (cGMP), a key molecule in the activation of type II
cGMP-dependent protein kinase
(
PKG II
). In our previous study, the membrane-permeable cGMP analogue 8-pCPT-cGMP was used to activate
PKG II
. The aim of the present study was to investigate whether NO/sGC-induced endogenous cGMP is able to activate
PKG II
and induce the corresponding effects. In the AGS gastric cancer cell line, the expression of
PKG II
was increased by infecting the cells with an adenoviral construct encoding
PKG II
cDNA (Ad-
PKG II
) and the activation of
PKG II
was induced by 8-pCPT-cGMP (positive control), the NO donor sodium nitroprusside (SNP) and the NO precursor L-arginine. ELISA was performed to detect the concentration of cGMP in AGS cells and the Cell Counting Kit-8 was used to analyze the proliferation of differently treated cells. Western blot analysis was used to detect the expression and phosphorylation of associated proteins. The results demonstrated that the level of cGMP was increased in cells treated with the NO donor or precursor. There was an obvious increase of Ser239 phosphorylation of the vasodilator-stimulated phosphoprotein, representing the increase in the activity of
PKG II
. The epidermal growth factor (EGF)-induced proliferation of AGS cells was inhibited by infection with Ad-
PKG II
and treatment with SNP or L-arginine. In addition, EGF-induced tyrosine phosphorylation of the EGF receptor (EGFR) and
tyrosine/serine
phosphorylation of extracellular signal-regulated kinase (ERK) were also inhibited by infection with Ad-
PKG II
and treatment with the NO donor or precursor. These data indicated that NO donors and precursors may activate the expression of
PKG II
, thereby blocking EGF-initiated signaling of the mitogen-activated protein kinase/ERK pathway and inhibiting EGF-induced proliferative activity through preventing the phosphorylation of EGFR at tyr1068.
...
PMID:Nitric oxide/cyclic guanosine monophosphate inducers sodium nitroprusside and L-arginine inhibit the proliferation of gastric cancer cells via the activation of type II cyclic guanosine monophosphate-dependent protein kinase. 2617 Oct 55