TY - JOUR
T1 - Raf kinase inhibitor protein RKIP enhances signaling by glycogen synthase kinase-3β
AU - Al-Mulla, Fahd
AU - Bitar, Milad S.
AU - Al-Maghrebi, May
AU - Behbehani, Abdulla I.
AU - Al-Ali, Waleed
AU - Rath, Oliver
AU - Doyle, Brendan
AU - Tan, Kit Yee
AU - Pitt, Andrew
AU - Kolch, Walter
PY - 2011/2/15
Y1 - 2011/2/15
N2 - Raf kinase inhibitory protein (RKIP) is a physiologic inhibitor of c-RAF kinase and nuclear factor κB signaling that represses tumor invasion and metastasis. Glycogen synthase kinase-3β (GSK3β) suppresses tumor progression by downregulating multiple oncogenic pathways including Wnt signaling and cyclin D1 activation. Here, we show that RKIP binds GSK3 proteins and maintains GSK3β protein levels and its active form. Depletion of RKIP augments oxidative stress-mediated activation of the p38 mitogen activated protein kinase, which, in turn, inactivates GSK3β by phosphorylating it at the inhibitory T390 residue. This pathway de-represses GSK3β inhibition of oncogenic substrates causing stabilization of cyclin D, which induces cell-cycle progression and β-catenin, SNAIL, and SLUG, which promote epithelial to mesenchymal transition. RKIP levels in human colorectal cancer positively correlate with GSK3β expression. These findings reveal the RKIP/GSK3 axis as both a potential therapeutic target and a prognosis-based predictor of cancer progression.
AB - Raf kinase inhibitory protein (RKIP) is a physiologic inhibitor of c-RAF kinase and nuclear factor κB signaling that represses tumor invasion and metastasis. Glycogen synthase kinase-3β (GSK3β) suppresses tumor progression by downregulating multiple oncogenic pathways including Wnt signaling and cyclin D1 activation. Here, we show that RKIP binds GSK3 proteins and maintains GSK3β protein levels and its active form. Depletion of RKIP augments oxidative stress-mediated activation of the p38 mitogen activated protein kinase, which, in turn, inactivates GSK3β by phosphorylating it at the inhibitory T390 residue. This pathway de-represses GSK3β inhibition of oncogenic substrates causing stabilization of cyclin D, which induces cell-cycle progression and β-catenin, SNAIL, and SLUG, which promote epithelial to mesenchymal transition. RKIP levels in human colorectal cancer positively correlate with GSK3β expression. These findings reveal the RKIP/GSK3 axis as both a potential therapeutic target and a prognosis-based predictor of cancer progression.
UR - http://www.scopus.com/inward/record.url?scp=79951842545&partnerID=8YFLogxK
U2 - 10.1158/0008-5472.CAN-10-3102
DO - 10.1158/0008-5472.CAN-10-3102
M3 - Article
C2 - 21303975
AN - SCOPUS:79951842545
SN - 0008-5472
VL - 71
SP - 1334
EP - 1343
JO - Cancer Research
JF - Cancer Research
IS - 4
ER -