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MYLIP — TCF24
Text-mined interactions from Literome
Gao et al., Nature 2009
:
Here we report that the c-Myc ( hereafter referred to as Myc ) oncogenic
transcription factor , which is known to regulate microRNAs and stimulate cell proliferation, transcriptionally
represses miR-23a and miR-23b, resulting in greater expression of their target protein, mitochondrial glutaminase, in human P-493 B lymphoma cells and PC3 prostate cancer cells
Yoo et al., Nature 2009
:
Previous studies have indicated that
miR-9* and miR-124 are
repressed by the repressor-element-1 silencing
transcription factor ( REST, also known as NRSF )
Reddy et al., Cancer Res 2009
(Neoplasms, Experimental) :
We found that endogenous
miR-661 expression was positively
regulated by the c/EBPalpha
transcription factor , which is down-regulated during cancer progression
Christoffersen et al., Cell Death Differ 2010
(Neoplasms) :
Instead, upregulation of
miR-34a is
mediated by the ETS family
transcription factor , ELK1
Ohdaira et al., Comput Biol Chem 2009
(Lung Neoplasms) :
Using a luciferase reporter assay, we also showed that
hsa-miR-601 specifically
repressed nuclear factor-kappaB (NF-kappaB)
transcription factor dependent reporter expression, a key component of the immune-oncogenesis pathway
Garofalo et al., Cancer Cell 2009
(Carcinoma, Non-Small-Cell Lung...) :
Finally, we demonstrate that the MET oncogene is involved in
miR-221 & 222
activation through the c-Jun
transcription factor
Hu et al., Proc Natl Acad Sci U S A 2010
(Neuroblastoma) :
Overexpression of the N-Myc
transcription factor , an oncogene frequently amplified in neuroblastoma,
induced miR-421 expression, which, in turn, down-regulated ATM expression, establishing a linear signaling pathway that may contribute to N-Myc induced tumorigenesis in neuroblastoma
Mardaryev et al., FASEB J 2010
:
Microarray, qRT-PCR and Western blot analyses revealed that
miR-31 negatively
regulates expression of Fgf10, the components of Wnt and BMP signaling pathways Sclerostin and BAMBI, and Dlx3
transcription factor , as well as selected keratin genes, both in vitro and in vivo
Ponomarev et al., Nat Med 2011
(Encephalomyelitis, Autoimmune, Experimental...) :
When overexpressed in macrophages,
miR-124 directly
inhibited the
transcription factor CCAAT/enhancer binding protein-a ( C/EBP-a ) and its downstream target PU.1, resulting in transformation of these cells from an activated phenotype into a quiescent CD45 ( low ), major histocompatibility complex ( MHC) class II(low ) phenotype resembling resting microglia
Ren et al., Plant Sci 2012
:
Sucrose induces the expression of miR398 and the production of
miR398 is
controlled by SQUAMOSA promoter binding protein-like7 ( SPL7 )
transcription factor under copper deficiency in Arabidopsis thaliana
Dong et al., RNA 2012
:
Coat color determination by
miR-137 mediated down-regulation of microphthalmia associated
transcription factor in a mouse model
Nahid et al., J Immunol 2013
:
The rapid induction of
miR-132/-212 was
transcription factor CREB
dependent , and the sustained expression of miR-132/-212 was responsible for inducing tolerance to subsequent PGN challenge
Melo et al., Nat Cell Biol 2013
(Breast Neoplasms) :
The GATA3
transcription factor is now shown to
regulate the tumour microenvironment by inducing the expression of
miR-29b in cancer cells
Shirasaki et al., J Virol 2013
(Carcinoma, Hepatocellular...) :
Gene expression profiling of Huh-7.5 cells showed that
miR-27a regulates lipid metabolism by targeting the lipid synthetic
transcription factor RXRa and the lipid transporter ATP binding cassette subfamily A member 1
Gebeshuber et al., Nat Med 2013
(Glomerulosclerosis, Focal Segmental) :
Mechanistically,
miR-193a inhibits the expression of the Wilms' tumor protein ( WT1 ), a
transcription factor and master regulator of podocyte differentiation and homeostasis