+ |
CXCL12 | up-regulates
binding
|
ACKR3 |
0.713 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-139709 |
|
|
Homo sapiens |
T-lymphocyte |
pmid |
sentence |
16107333 |
Here we show that cxcl12, the only known natural ligand for cxcr4, binds to and signals through rdc1. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
CXCL12 | up-regulates
binding
|
CXCR4 |
0.805 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-115029 |
|
|
Homo sapiens |
|
pmid |
sentence |
11859124 |
To study the role of the sdf-1/cxcr4-chemokine/receptor system as a regulator of vertebrate development, we isolated and characterized a cdna encoding sdf-1 of the lower vertebrate xenopus laevis (xsdf-1). Recombinant xsdf-1 was produced in insect cells, purified, and functionally characterized. Although xsdf-1 is only 64-66% identical with its mammalian counterparts, it is indistinguishable from human (h)sdf-1alpha in terms of activating both x. laevis cxcr4 and hcxcr4. Thus, both xsdf-1 and hsdf-1alpha promoted cxcr4-mediated activation of heterotrimeric g(i2) in a cell-free system and induced release of intracellular calcium ions in and chemotaxis of intact lymphoblastic cells. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
hsa-miR-1-5p | down-regulates quantity by repression
post transcriptional regulation
|
CXCL12 |
0.4 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-277927 |
|
|
Homo sapiens |
Thyroid Cancer Cell |
pmid |
sentence |
21752897 |
We also show that miR-1 transfection down-regulates the luciferase activity of a reporter construct carrying the 3′-UTR-CXCR4 or 3′-UTR-SDF-1α sequence. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
CXCL12 | up-regulates
|
Angiogenesis |
0.7 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-252267 |
|
|
Homo sapiens |
MCF-7 Cell |
pmid |
sentence |
15882617 |
Stromal fibroblast-derived SDF-1 enhances tumor growth both by stimulating angiogenesis through recruiting circulating EPCs into the tumor mass (endocrine effect) and by direct paracrine stimulation of tumor cells through CXCR4 expressed on carcinoma cells |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
hsa-miR-101-5p | down-regulates quantity by repression
post transcriptional regulation
|
CXCL12 |
0.4 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-278008 |
|
|
Homo sapiens |
A-549 Cell |
pmid |
sentence |
26349988 |
MiR-101 suppressed the transcription activity of the CXCL12 gene by targeting the binding site in the 3'UTR of CXCL12 mRNA independently. | We observed that upon transfection with miR-101, the expression of CXCL12 protein and mRNA were both decreased. Collectively, these findings suggest that miR-101 regulates the expression of CXCL12 post-transcriptionally. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
hsa-mir-126-5p | down-regulates quantity by repression
post transcriptional regulation
|
CXCL12 |
0.4 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-278009 |
|
|
Homo sapiens |
LAMA-84 Cell |
pmid |
sentence |
25015105 |
In this study, we show that miR-126 transferred to endothelial cells via LAMA84 exosomes directly targets the 3’ UTR of CXCL12 and VCAM1 mRNA, significantly down-regulating the expression and function of both proteins. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
SNAI2 | up-regulates quantity by expression
transcriptional regulation
|
CXCL12 |
0.418 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-255169 |
|
|
Homo sapiens |
Prostate Cancer Cell Line |
pmid |
sentence |
22074556 |
We demonstrated that forced expression of SLUG elevated CXCR4 and CXCL12 expression in human prostate cancer cell lines PC3, DU145, 22RV1, and LNCaP; conversely, reduced expression of SLUG by shRNA downregulated CXCR4 and CXCL12 expression at RNA and protein levels in prostate cancer cells. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |