◀ Back to RELA
RELA — SETD2
Text-mined interactions from Literome
Figueroa et al., Exp Hematol 2002
(Anoxia) :
The selective inhibitor of
NF-kappaB , pyrrolidine dithiocarbamate ( PDTC ), significantly
blocked HIF-1 protein expression ... Inhibition of
NF-kappaB with a superrepressor dominant negative IkappaBalpha genetic construct also significantly
blocked NF-kappaB and
HIF-1 transactivation, as well as EPO gene expression
Tacchini et al., Carcinogenesis 2004
(Breast Neoplasms...) :
Hepatocyte growth factor activated
NF-kappaB regulates
HIF-1 activity and ODC expression, implicated in survival, differently in different carcinoma cell lines
Nishi et al., Antioxid Redox Signal 2008
:
LPS mediated activation of
HIF-1 was
independent of
NF-kappaB activity
Scortegagna et al., Blood 2008
(Drug Hypersensitivity...) :
HIF-1 induced
NFkappaB activation was composed of 2 elements, IkappaB hyperphosphorylation and phosphorylation of Ser276 on p65, enhancing p65 nuclear localization and transcriptional activity, respectively
Bendinelli et al., Mol Cancer Res 2009
(Bone Neoplasms...) :
NF-kappaB activation, dependent on acetylation/deacetylation,
contributes to
HIF-1 activity and migration of bone metastatic breast carcinoma cells
Kumar et al., PloS one 2012
:
Inhibition of TG2 or
p65/RelA also
inhibited the
HIF-1a expression and attenuated Zeb1, Zeb2, and Twist expression
Tafani et al., Frontiers in pharmacology 2013
:
Interestingly, hypoxia and inflammation have been sequentially bridged in tumors by the discovery that alarmin receptors genes such as RAGE, P2X7, and some TLRs, are activated by
HIF1a ; and that, in turn, alarmin receptors strongly
activate NFkB and proinflammatory gene expression, evidencing all the hallmarks of the malignant phenotype