◀ Back to EPHB2
EPHB2 — LDLR
Text-mined interactions from Literome
Kong et al., Nat Med 2004
(Hypercholesterolemia) :
Using human hepatoma cells, we show that BBR upregulates
LDLR expression independent of sterol regulatory element binding proteins, but
dependent on
ERK activation
Abidi et al., Arterioscler Thromb Vasc Biol 2005
(Carcinoma, Hepatocellular...) :
Using different reporter constructs, we demonstrate that BBR affects
LDLR mRNA stability entirely through 3 ' untranslated region ( UTR ) in an
ERK dependent manner, and this stabilizing effect is more prominent in liver derived cells than nonhepatic cell lines
Lu et al., J Agric Food Chem 2008
(Hypercholesterolemia) :
Collectively, these new findings identify gossypin as a new hypocholesterolemic agent that up-regulates
LDLR expression independent of SREBP-2 but is
dependent on
ERK activation
Xiong et al., PLoS Pathog 2009
(Ehrlichiosis) :
Up-regulation of LDLR mRNA by A. phagocytophilum was also inhibited by the MEK inhibitor ; however, it was unclear whether
ERK activation is
required for
LDLR mRNA up-regulation by A. phagocytophilum
Duan et al., J Biol Chem 2012
:
However, PPAR? activation by ligands or
ERK1/2 inhibitors
induced hepatic
LDLR expression
Kumar et al., J Lipid Res 1997
:
Moreover, pretreatment of cells with calphostin C inhibited TPA mediated
ERK activation and
LDL receptor mRNA
induction in a dose dependent fashion