| + |
ZC3H12A | up-regulates quantity
post transcriptional regulation
|
GATA2 |
0.2 |
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-259943 |
|
|
Homo sapiens |
HEK-293 Cell |
| pmid |
sentence |
| 30842549 |
Here, we show that Regnase-1 regulates self-renewal of HSPCs through modulating the stability of Gata2 and Tal1 mRNA |
|
| Publications: |
1 |
Organism: |
Homo Sapiens |
| + |
ZC3H12A | up-regulates quantity
post transcriptional regulation
|
TAL1 |
0.2 |
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-259944 |
|
|
Homo sapiens |
HEK-293 Cell |
| pmid |
sentence |
| 30842549 |
Here, we show that Regnase-1 regulates self-renewal of HSPCs through modulating the stability of Gata2 and Tal1 mRNA |
|
| Publications: |
1 |
Organism: |
Homo Sapiens |
| + |
ZC3H12A | down-regulates quantity by destabilization
post transcriptional regulation
|
TGFB1 |
0.2 |
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-282641 |
|
|
Homo sapiens |
PANC-1 Cell |
| pmid |
sentence |
| 37814340 |
Pancreatitis is known to be an important risk factor for pancreatic ductal adenocarcinoma (PDAC). However, the exact molecular mechanisms of how inflammation promotes PDAC are still not fully understood. Regnase-1, an endoribonuclease, regulates immune responses by degrading mRNAs of inflammation-related genes. Herein, we investigated the role of Regnase-1 in PDAC.Mechanistically, Regnase-1 directly negatively regulated a variety of chemokines/cytokines important for MDSC recruitment and activation, including CXCL1, CXCL2, CSF2, and TGFβ, in pancreatic cancer cells. |
|
| Publications: |
1 |
Organism: |
Homo Sapiens |
| + |
ZC3H12A | down-regulates quantity by destabilization
post transcriptional regulation
|
CXCL1 |
0.288 |
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-282638 |
|
|
Homo sapiens |
PANC-1 Cell |
| pmid |
sentence |
| 37814340 |
Pancreatitis is known to be an important risk factor for pancreatic ductal adenocarcinoma (PDAC). However, the exact molecular mechanisms of how inflammation promotes PDAC are still not fully understood. Regnase-1, an endoribonuclease, regulates immune responses by degrading mRNAs of inflammation-related genes. Herein, we investigated the role of Regnase-1 in PDAC.Mechanistically, Regnase-1 directly negatively regulated a variety of chemokines/cytokines important for MDSC recruitment and activation, including CXCL1, CXCL2, CSF2, and TGFβ, in pancreatic cancer cells. |
|
| Publications: |
1 |
Organism: |
Homo Sapiens |
| + |
ZC3H12A | down-regulates quantity by destabilization
post transcriptional regulation
|
CXCL2 |
0.293 |
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-282639 |
|
|
Homo sapiens |
PANC-1 Cell |
| pmid |
sentence |
| 37814340 |
Pancreatitis is known to be an important risk factor for pancreatic ductal adenocarcinoma (PDAC). However, the exact molecular mechanisms of how inflammation promotes PDAC are still not fully understood. Regnase-1, an endoribonuclease, regulates immune responses by degrading mRNAs of inflammation-related genes. Herein, we investigated the role of Regnase-1 in PDAC.Mechanistically, Regnase-1 directly negatively regulated a variety of chemokines/cytokines important for MDSC recruitment and activation, including CXCL1, CXCL2, CSF2, and TGFβ, in pancreatic cancer cells. |
|
| Publications: |
1 |
Organism: |
Homo Sapiens |
| + |
ZC3H12A | down-regulates quantity by destabilization
post transcriptional regulation
|
CSF2 |
0.252 |
| Identifier |
Residue |
Sequence |
Organism |
Cell Line |
| SIGNOR-282640 |
|
|
Homo sapiens |
PANC-1 Cell |
| pmid |
sentence |
| 37814340 |
Pancreatitis is known to be an important risk factor for pancreatic ductal adenocarcinoma (PDAC). However, the exact molecular mechanisms of how inflammation promotes PDAC are still not fully understood. Regnase-1, an endoribonuclease, regulates immune responses by degrading mRNAs of inflammation-related genes. Herein, we investigated the role of Regnase-1 in PDAC.Mechanistically, Regnase-1 directly negatively regulated a variety of chemokines/cytokines important for MDSC recruitment and activation, including CXCL1, CXCL2, CSF2, and TGFβ, in pancreatic cancer cells. |
|
| Publications: |
1 |
Organism: |
Homo Sapiens |