+ |
FZD9 | down-regulates quantity by repression
transcriptional regulation
|
SPRY4 |
0.285 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-253035 |
|
|
Homo sapiens |
|
pmid |
sentence |
15705594 |
In NSCLC cells, Wnt-7a and Fzd-9 induced both cadherin and Sprouty-4 expression and stimulated the JNK pathway, but not beta-catenin/T cell factor activity. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
SPRY4 | down-regulates activity
binding
|
TESK1 |
0.583 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-253032 |
|
|
Homo sapiens |
|
pmid |
sentence |
15584898 |
Spry4 negatively regulates the kinase activity of TESK1 by associating with it through the C-terminal cysteine-rich region of Spry4 |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
SPRY4 | up-regulates quantity by expression
transcriptional regulation
|
TIMP1 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-253038 |
|
|
Homo sapiens |
Non-small Cell Lung Cancer Cell |
pmid |
sentence |
20501643 |
When Spry4 was stably transfected into H157 and H2122 NSCLC cell lines, decreased migration and invasion were observed. Matrix metalloproteinase-9 activity was decreased, and the expression of matrix metalloproteinase inhibitors TIMP1 and CD82 were increased. Stable expression of Spry4 led to reduced cell growth and reduced anchorage-independent growth in NSCLC cell lines, along with upregulation of tumor suppressors p53 and p21. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
SPRY4 | up-regulates quantity by expression
transcriptional regulation
|
CDKN1A |
0.254 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-253041 |
|
|
Homo sapiens |
Non-small Cell Lung Cancer Cell |
pmid |
sentence |
20501643 |
When Spry4 was stably transfected into H157 and H2122 NSCLC cell lines, decreased migration and invasion were observed. Matrix metalloproteinase-9 activity was decreased, and the expression of matrix metalloproteinase inhibitors TIMP1 and CD82 were increased. Stable expression of Spry4 led to reduced cell growth and reduced anchorage-independent growth in NSCLC cell lines, along with upregulation of tumor suppressors p53 and p21. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
SPRY4 | up-regulates quantity by expression
transcriptional regulation
|
TP53 |
0.271 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-253040 |
|
|
Homo sapiens |
Non-small Cell Lung Cancer Cell |
pmid |
sentence |
20501643 |
When Spry4 was stably transfected into H157 and H2122 NSCLC cell lines, decreased migration and invasion were observed. Matrix metalloproteinase-9 activity was decreased, and the expression of matrix metalloproteinase inhibitors TIMP1 and CD82 were increased. Stable expression of Spry4 led to reduced cell growth and reduced anchorage-independent growth in NSCLC cell lines, along with upregulation of tumor suppressors p53 and p21. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
SPRY4 | down-regulates activity
|
MMP9 |
0.271 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-253037 |
|
|
Homo sapiens |
Non-small Cell Lung Cancer Cell |
pmid |
sentence |
20501643 |
When Spry4 was stably transfected into H157 and H2122 NSCLC cell lines, decreased migration and invasion were observed. Matrix metalloproteinase-9 activity was decreased, and the expression of matrix metalloproteinase inhibitors TIMP1 and CD82 were increased. Stable expression of Spry4 led to reduced cell growth and reduced anchorage-independent growth in NSCLC cell lines, along with upregulation of tumor suppressors p53 and p21. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
SPRY4 | up-regulates quantity by expression
transcriptional regulation
|
CD82 |
0.2 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-253039 |
|
|
Homo sapiens |
Non-small Cell Lung Cancer Cell |
pmid |
sentence |
20501643 |
When Spry4 was stably transfected into H157 and H2122 NSCLC cell lines, decreased migration and invasion were observed. Matrix metalloproteinase-9 activity was decreased, and the expression of matrix metalloproteinase inhibitors TIMP1 and CD82 were increased. Stable expression of Spry4 led to reduced cell growth and reduced anchorage-independent growth in NSCLC cell lines, along with upregulation of tumor suppressors p53 and p21. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
SPRY4 | down-regulates activity
binding
|
RAF1 |
0.444 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-253033 |
|
|
Homo sapiens |
|
pmid |
sentence |
12717443 |
Here we show that mammalian Sprouty4 suppresses vascular epithelial growth factor (VEGF)-induced, Ras-independent activation of Raf1 but does not affect epidermal growth factor (EGF)-induced, Ras-dependent activation of Raf1. Sprouty4 binds to Raf1 through its carboxy-terminal cysteine-rich domain, and this binding is necessary for the inhibitory activity of Sprouty4. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
SPRY4 | down-regulates
|
Epithelial-mesenchymal_transition |
0.7 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-253036 |
|
|
Homo sapiens |
Non-small Cell Lung Cancer Cell |
pmid |
sentence |
20501643 |
Spry4 expression induces a reversal of the epithelial to mesenchymal transition characteristic of tumor cells. Treatment of a non-transformed lung epithelial cell line with shRNA to Spry4 led to decreased expression of epithelial markers and increased cell growth, supporting the concept of Spry4 acting as a tumor suppressor. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |
+ |
WNT7A | down-regulates quantity by repression
transcriptional regulation
|
SPRY4 |
0.279 |
Identifier |
Residue |
Sequence |
Organism |
Cell Line |
SIGNOR-253034 |
|
|
Homo sapiens |
Non-small Cell Lung Cancer Cell |
pmid |
sentence |
15705594 |
In NSCLC cells, Wnt-7a and Fzd-9 induced both cadherin and Sprouty-4 expression and stimulated the JNK pathway, but not beta-catenin/T cell factor activity. |
|
Publications: |
1 |
Organism: |
Homo Sapiens |