+ |
HIC1 | down-regulates quantity by repression
transcriptional regulation
|
SIRT1 |
0.607 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-254419 |
|
|
Homo sapiens |
|
pmid |
sentence |
21277938 |
HIC1, via its BTB/POZ domain, forms a transcriptional repressor complex with Sirt1 [8] that binds directly to Sirt1 promoter itself, repressing its transcription. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
HIC1 | down-regulates quantity by repression
transcriptional regulation
|
ACKR3 |
0.29 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-254238 |
|
|
Homo sapiens |
|
pmid |
sentence |
23340301 |
we showed that CXCR7 promoter in prostate cancer cells is negatively regulated by HIC1, which may be responsible for prostate cancer progression. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
HIC1 | down-regulates quantity by repression
transcriptional regulation
|
E2F1 |
0.293 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-254239 |
|
|
Homo sapiens |
Fibroblast |
pmid |
sentence |
19486893 |
HIC1 is also implicated in growth control since it recruits BRG1, one of the two alternative ATPases (BRM or BRG1) of SWI/SNF chromatin-remodeling complexes to repress transcription of E2F1 in quiescent fibroblasts. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
HIC1 | down-regulates quantity by repression
transcriptional regulation
|
EFNA1 |
0.369 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-254240 |
|
|
Homo sapiens |
|
pmid |
sentence |
20154726 |
we show that HIC1 is a direct transcriptional repressor of the gene encoding ephrin-A1, a cell surface ligand implicated in the pathogenesis of epithelial cancers. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
HIC1 | down-regulates quantity by repression
transcriptional regulation
|
VEGFA |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-254247 |
|
|
Homo sapiens |
MDA-MB-231 Cell |
pmid |
sentence |
24067369 |
HIC1 suppressing the VEGF and c-Myc promoter activity and the colony formation of MDA-MB 231 cells were STAT3-dependent. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
HIC1 | down-regulates quantity by repression
transcriptional regulation
|
VLDLR |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-254244 |
|
|
Homo sapiens |
U2-OS Cell, MDA-MB-231 Cell |
pmid |
sentence |
24076391 |
The Reelin receptors ApoER2 and VLDLR are direct target genes of HIC1. ectopic expression of HIC1 in U2OS and MDA-MB-231 cell lines decreases expression of the ApoER2 and VLDLR genes, encoding two canonical tyrosine kinase receptors for Reelin. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
HIC1 | down-regulates activity
transcriptional regulation
|
MYC |
0.33 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-254245 |
|
|
Homo sapiens |
MDA-MB-231 Cell |
pmid |
sentence |
24067369 |
HIC1 suppressing the VEGF and c-Myc promoter activity and the colony formation of MDA-MB 231 cells were STAT3-dependent. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
HIC1 | down-regulates quantity by repression
transcriptional regulation
|
LRP8 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-254243 |
|
|
Homo sapiens |
U2-OS Cell, MDA-MB-231 Cell |
pmid |
sentence |
24076391 |
The Reelin receptors ApoER2 and VLDLR are direct target genes of HIC1. ectopic expression of HIC1 in U2OS and MDA-MB-231 cell lines decreases expression of the ApoER2 and VLDLR genes, encoding two canonical tyrosine kinase receptors for Reelin. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
HIC1 | down-regulates quantity by repression
binding
|
STAT3 |
0.375 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-254246 |
|
|
Homo sapiens |
MDA-MB-231 Cell |
pmid |
sentence |
24067369 |
HIC1 interacts with the DNA binding domain of STAT3 and suppresses the binding of STAT3 to its target gene promoters. HIC1 C-terminal domain binds to STAT3. HIC1 mutant defective in STAT3 interaction reduced its repressive effect on STAT3 DNA binding activity, the reporter activity and gene expression of the VEGF and c-Myc genes, and cell growth in MDA-MB 231 cells. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
E2F1 | up-regulates quantity by expression
transcriptional regulation
|
HIC1 |
0.293 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-253844 |
|
|
Homo sapiens |
|
pmid |
sentence |
19491197 |
expression of E2F1 in the p53(-/-) hepatocellular carcinoma cell line Hep3B led to an increase of endogenous HIC1 mRNA, although bisulfite genomic sequencing of the HIC1 promoter revealed that the region bearing the two E2F1 binding sites is hypermethylated. In addition, endogenous E2F1 induced by etoposide treatment bound to the HIC1 promoter. Moreover, inhibition of E2F1 strongly reduced the expression of etoposide-induced HIC1. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
HIC1 | down-regulates quantity by repression
transcriptional regulation
|
EPHA2 |
0.319 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-254241 |
|
|
Homo sapiens |
Breast Epithelial Cell |
pmid |
sentence |
22184117 |
The receptor tyrosine kinase EphA2 is a direct target gene of hypermethylated in cancer 1 (HIC1). we observe that inactivation of endogenous HIC1 through RNA interference in normal breast epithelial cells results in the up-regulation of EphA2 and is correlated with increased cellular migration. chromatin immunoprecipitation (ChIP) and sequential ChIP experiments demonstrate that endogenous HIC1 proteins are bound, together with the MTA1 corepressor, to the EphA2 promoter in WI38 cells. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |