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:2.7.12.2 (
MEK
)
18,161
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Loss of tumor suppressor activity and upregulation of oncogenic pathways simultaneously contribute to tumorigenesis. Expression of the tumor suppressor,
GCIP
(Grap2- and cyclin D1-interacting protein), is usually reduced or lost in advanced cancers, as seen in both mouse tumor models and human cancer patients. However, no previous study has examined how cancer cells down-regulate
GCIP
expression. In this study, we first validate the tumor suppressive function of
GCIP
using clinical gastric cancer tissues and online database analysis. We then reveal a novel mechanism whereby
MEK2
directly interacts with and phosphorylates
GCIP
at its Ser313 and Ser356 residues to promote the turnover of
GCIP
by ubiquitin-mediated proteasomal degradation. We also reveal that decreased
GCIP
stability enhances cell proliferation and promotes cancer cell migration and invasion. Taken together, these findings provide a more comprehensive view of
GCIP
in tumorigenesis and suggest that the oncogenic
MEK
/ERK signaling pathway negatively regulates the protein level of
GCIP
to promote cell proliferation and migration.
...
PMID:MEK2 is a critical modulating mechanism to down-regulate GCIP stability and function in cancer cells. 3190 80