Glioblastoma Multiforme
|
0.550 |
GeneticVariation
|
disease |
UNIPROT |
|
|
|
Metastatic melanoma
|
0.300 |
GeneticVariation
|
disease |
UNIPROT |
|
|
|
Malignant neoplasm of breast
|
0.100 |
Biomarker
|
disease |
BEFREE |
<i>FAK</i>-copy-gain may be a predictive marker for FAK inhibition therapy in breast cancer.
|
31480645 |
2019 |
Breast Carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
<i>FAK</i>-copy-gain may be a predictive marker for FAK inhibition therapy in breast cancer.
|
31480645 |
2019 |
Malignant neoplasm of breast
|
0.100 |
Biomarker
|
disease |
BEFREE |
<i>In vitro</i> experiments showed that tyrosine phosphorylation of CSF-1R, ERK, and FAK and cell migration are differentially regulated by IL-34 and CSF-1 in breast cancer cell lines.
|
29796177 |
2018 |
Breast Carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
<i>In vitro</i> experiments showed that tyrosine phosphorylation of CSF-1R, ERK, and FAK and cell migration are differentially regulated by IL-34 and CSF-1 in breast cancer cell lines.
|
29796177 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
1204-1216) use elegant genetic approaches to simultaneously delete the essential autophagy gene FIP200 (FAK family-interacting protein of 200 kDa) and the signaling adaptor p62/SQSTM1 within established murine tumors, which reveals an unexpected synergism between the autophagy pathway and p62 in driving tumor growth.
|
24888584 |
2014 |
Malignant Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
5'-NIO inhibited the beta1 Integrin/FAK/Akt pathway which can then facilitate invasion and/or migration of cancer cells through the extracellular matrix (ECM).
|
21463917 |
2011 |
Primary malignant neoplasm
|
0.100 |
Biomarker
|
group |
BEFREE |
5'-NIO inhibited the beta1 Integrin/FAK/Akt pathway which can then facilitate invasion and/or migration of cancer cells through the extracellular matrix (ECM).
|
21463917 |
2011 |
Hypocholesterolemia
|
0.010 |
PosttranslationalModification
|
disease |
BEFREE |
Cholesterol depletion inhibited phosphorylation of Src on Y416 in the detergent-insoluble fraction followed by decreased localization of total and pY397 FAK in the detergent-insoluble fraction.
|
19945766 |
2010 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Tumors sensitive to saracatinib showed an increase in the activation of Src and FAK when compared with resistant tumors.
|
20682712 |
2010 |
Liver carcinoma
|
0.600 |
Biomarker
|
disease |
LHGDN |
FAK proteins were detected in all HCC cell lines.
|
15102689 |
2004 |
Adenocarcinoma of pancreas
|
0.010 |
PosttranslationalModification
|
disease |
BEFREE |
FAK gene silencing suppresses anoikis resistance in pancreatic adenocarcinoma cells.
|
15118593 |
2004 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
FAK protein overexpression in tumors correlated with nodal metastases.
|
16740747 |
2006 |
Neoplasm Metastasis
|
0.300 |
AlteredExpression
|
phenotype |
BEFREE |
FAK protein overexpression in tumors correlated with nodal metastases.
|
16740747 |
2006 |
Secondary Neoplasm
|
0.070 |
AlteredExpression
|
group |
BEFREE |
FAK protein overexpression in tumors correlated with nodal metastases.
|
16740747 |
2006 |
Neuroblastoma
|
0.040 |
AlteredExpression
|
disease |
BEFREE |
FAK protein expression also correlated positively with N-MYC expression in the N-MYC-amplified IMR-32 versus nonamplified SK-N-AS neuroblastoma cell lines.
|
17327229 |
2007 |
Central neuroblastoma
|
0.040 |
AlteredExpression
|
disease |
BEFREE |
FAK protein expression also correlated positively with N-MYC expression in the N-MYC-amplified IMR-32 versus nonamplified SK-N-AS neuroblastoma cell lines.
|
17327229 |
2007 |
Childhood Neuroblastoma
|
0.040 |
AlteredExpression
|
disease |
BEFREE |
FAK protein expression also correlated positively with N-MYC expression in the N-MYC-amplified IMR-32 versus nonamplified SK-N-AS neuroblastoma cell lines.
|
17327229 |
2007 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
FAK is overexpressed in human tumors and regulates cellular adhesion and survival signaling.
|
17849451 |
2008 |
Tumor Angiogenesis
|
0.030 |
Biomarker
|
phenotype |
BEFREE |
FAK was held responsible for cancer cells' uninhibited proliferation, protection from apoptosis, invasion, migration, adhesion and spreading, as well as tumor angiogenesis.
|
18283648 |
2008 |
Mammary Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
FAK mRNA expression was also found to correlate with TP53 mutation status in a series of breast tumors.
|
21071137 |
2011 |
Malignant Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
FAK1 is known to enhance migration of cancer cells and promote metastatic dissemination to distant sites.
|
21707507 |
2011 |
Primary malignant neoplasm
|
0.100 |
Biomarker
|
group |
BEFREE |
FAK1 is known to enhance migration of cancer cells and promote metastatic dissemination to distant sites.
|
21707507 |
2011 |
Primary malignant neoplasm
|
0.100 |
Biomarker
|
group |
BEFREE |
FAK and WNT signaling: the meeting of two pathways in cancer and development.
|
21707509 |
2011 |