Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Furthermore, high expression of cytoplasmic ph-FAK Y<sup>925</sup> was associated with decreased tumour grade (P < .001), less involved lymph node (P = .020), molecular subtypes (P < .001), decreased tumour necrosis (P < .001), low Klintrup-Mäkinen grade (P < .001), decreased CD4+ T-cells (P = .006), decreased CD138+ plasma cells (P = .034), endocrine therapy (P < .001), chemotherapy (P = .048), and improved cancer specific survival (P = .044).
|
30981841 |
2019 |
Neoplasms
|
0.100 |
PosttranslationalModification
|
group |
BEFREE |
Accordingly, increased FAK tyrosine phosphorylation was observed within HGSOC patient tumors surviving neo-adjuvant chemotherapy.
|
31478830 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
These agents synergized to reduce tumor vascularity and endothelial cell growth and migration by blocking activation of FAK and SRC.
|
31841591 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Our study provides evidence that YAP acts as a promoter of focal adhesion and tumour invasiveness via regulating FAK phosphorylation in breast cancer.
|
30055645 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We demonstrated for the first time that TQ inhibits the protein and mRNA expression of eEF-2K, as well as the clinically relevant downstream targets, including Src/FAK and Akt, and induces the tumor suppressor miR-603, in response to NF-kB inhibition.
|
29971628 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
In addition, FAK expression was found to significantly correlate with tumor aggressiveness in sarcoma patient samples.
|
29190494 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
We developed a new co-culture model, using OS cells and mesenchymal stem cells (MSCs) without cellular contact, and found that both cell types expressed IL-8 at a high level, and FAK in OS cells was phosphorylated leading to an increase in the metastatic potential of the tumor in the co-culture condition.
|
29625612 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
QS-13 binding inhibits the FAK/PI<sub>3</sub>K/Akt pathway, a transduction pathway that is largely involved in tumor cell proliferation and migration.
|
29959360 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
The remodeling of the stromal matrix by CAFs has been shown to increase tumor rigidity to indirectly regulate FAK Y397 phosphorylation in tumor cells to promote their growth and invasion.
|
27893716 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Also, transplanted tumor formation experiment in nude mice was conducted to verify the effect of miR-433 and FAK on subcutaneous transplanted tumor.
|
29245973 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Recently, Jiang and colleagues identified a key role for FAK in regulating the composition of the fibrotic and immuno-suppressive pancreatic tumour niche, and showed that FAK inhibitors can be used in combination with immune checkpoint blockade and gemcitabine chemotherapy to significantly delay pancreatic tumour progression.
|
28239470 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Here we show that concomitant targeting of EGFR and the nonreceptor tyrosine kinases PYK2/FAK synergistically inhibits the proliferation of basal-like TNBC cells in vitro and attenuates tumor growth in a mouse xenograft model.
|
27793840 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
As recent reports imply that FAK1 is highly associated with tumor cell development and malignancy, the inhibition of FAK1 activity could be an effective therapeutic approach for inhibiting the growth and metastasis of tumor cells.
|
29048635 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
KCNMA1 cooperating with PTK2 is a novel tumor suppressor in gastric cancer and is associated with disease outcome.
|
28231797 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
SOX11 promotes tumor protective microenvironment interactions through CXCR4 and FAK regulation in mantle cell lymphoma.
|
28533307 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
For the study of the FAK targeted drug molecules, this was the first attempt to develop the tumor diagnostic imaging agents on the radiopharmaceutical level.
|
28109944 |
2017 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Expression data analysis of a large cohort of human breast tumors revealed that high expression of SMARCE1 or PTK2 is associated with poor prognosis and tumor relapse, and PTK2 expression is positively correlated with SMARCE1 expression in basal-like and luminal B subtypes of breast tumors.
|
27495308 |
2016 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
The activation of AKT and FAK facilitated tumor migration, invasion and accelerated cell growth.
|
27121319 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Caffeine reduced the invasion of glioma cells through ROCK-cathepsin B/FAK/ERK signaling pathway and tumor growth in orthotopic xenograft animal model, supporting the anti-cancer potential in glioma therapy.
|
27260469 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Moreover, the expression levels of beta-catenin, cyclin D1, c-Myc, MMP-2, and FAK detected by western blotting were downregulated in SLC5A8-transfected HCC cells compared with control-transfected cells, indicating that SLC5A8 has a tumor-suppressive function that acts by interfering with Wnt/β-catenin signaling in HCC.
|
27465549 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Zeb1-dependent EMT enhances tumor cell responsiveness to the ECM composition and activates FAK/Src pathway signaling by de-repression of the direct miR-200 target, CRKL.
|
26728244 |
2016 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Tivantinib (ARQ-197) exhibits anti-tumor activity with down-regulation of FAK in oral squamous cell carcinoma.
|
25623532 |
2015 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Furthermore, disruption of such complexes enhanced the survival of tumor-bearing mice in a xenograft model, and impaired activation of FAK and small GTPases.
|
26377974 |
2015 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
FAK gene amplification as a mechanism for FAK overexpression and the effects of FAK tyrosine kinase inhibitor VS-6062 on tumor growth, metastasis, and angiogenesis were examined.
|
24755674 |
2014 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Our collective observations provide evidence that a small molecule inhibitor targeted to the FAK protein-protein interaction site successfully inhibits melanoma growth through dual targeting of tumor and endothelial cells and is effective against both BRAF wild type and mutant melanomas.
|
25486195 |
2014 |