Neoplasm Metastasis
|
0.010 |
Biomarker
|
phenotype |
BEFREE |
In vitro and in vivo assay demonstrated that inhibition of STK17B markedly inhibits HCC tumorigenesis and metastasis, while STK17B overexpression promoted these processes.
|
29445189 |
2018 |
Carcinogenesis
|
0.010 |
Biomarker
|
phenotype |
BEFREE |
In vitro and in vivo assay demonstrated that inhibition of STK17B markedly inhibits HCC tumorigenesis and metastasis, while STK17B overexpression promoted these processes.
|
29445189 |
2018 |
Liver carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
In conclusion, our research demonstrated that STK17B promotes HCC progression, induces EMT process via activating AKT/GSK-3β/Snail signal and predicts poor prognosis in HCC.
|
29445189 |
2018 |
Diabetes
|
0.010 |
Biomarker
|
disease |
BEFREE |
These data support the notion that small molecule inhibitors of DRAK2 represents a promising strategy for the treatment of diabetes.
|
28249207 |
2017 |
Diabetes Mellitus
|
0.010 |
Biomarker
|
group |
BEFREE |
These data support the notion that small molecule inhibitors of DRAK2 represents a promising strategy for the treatment of diabetes.
|
28249207 |
2017 |
Autoimmune Diseases
|
0.010 |
Biomarker
|
group |
BEFREE |
These data further validate Drak2 as a viable therapeutic target to treat autoimmune disease and graft rejection.
|
25568303 |
2015 |
Diabetes Mellitus, Insulin-Dependent
|
0.010 |
Biomarker
|
disease |
BEFREE |
Drak2 is a promising therapeutic target to treat organ-specific autoimmune diseases such as type 1 diabetes and multiple sclerosis without causing generalized immune suppression.
|
25568303 |
2015 |
Multiple Sclerosis
|
0.010 |
Biomarker
|
disease |
BEFREE |
Drak2 is a promising therapeutic target to treat organ-specific autoimmune diseases such as type 1 diabetes and multiple sclerosis without causing generalized immune suppression.
|
25568303 |
2015 |
Neoplasms
|
0.010 |
AlteredExpression
|
group |
BEFREE |
Importantly, these data also indicate that while Drak2 may induce apoptosis when overexpressed in cell lines, it is not an essential tumor suppressor.
|
25568303 |
2015 |
IMMUNE SUPPRESSION
|
0.010 |
Biomarker
|
phenotype |
BEFREE |
Drak2 is a promising therapeutic target to treat organ-specific autoimmune diseases such as type 1 diabetes and multiple sclerosis without causing generalized immune suppression.
|
25568303 |
2015 |
Papillary thyroid carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
An epistatic interaction between the PAX8 and STK17B genes in papillary thyroid cancer susceptibility.
|
24086368 |
2013 |
Thyroid carcinoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Furthermore, we demonstrated an inverse correlation between expression of PAX8 and STK17B in a set of cell lines derived from human thyroid carcinomas.
|
24086368 |
2013 |
Mammary Neoplasms
|
0.010 |
AlteredExpression
|
group |
BEFREE |
Furthermore, a high level of DRAK2 expression was observed in basal-like and HER2-enriched breast tumors and cell lines, and depletion of DRAK2 expression suppressed the tumorigenic ability of breast cancer cells.
|
23122956 |
2012 |
Idiopathic Pulmonary Fibrosis
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
The expression of three genes (STK17B, STK3 and HIST1H2AH) with hypomethylated promoters was increased in IPF lungs.
|
22506007 |
2012 |
Colorectal Carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
In vitro silencing of DRAK2 by RNAi enhanced CRC cell survival following COX-2 inhibitor treatment.
|
19638987 |
2009 |
Malignant neoplasm of colon and/or rectum
|
0.010 |
Biomarker
|
disease |
BEFREE |
Regulation of the apoptosis-inducing kinase DRAK2 by cyclooxygenase-2 in colorectal cancer.
|
19638987 |
2009 |
Lymphoma, T-Cell, Cutaneous
|
0.010 |
Biomarker
|
disease |
BEFREE |
The expression pattern of the detected clones and their immunogenicity demonstrates that they might be relevant for the understanding of CTCL and suggests particularly three clones, HD-CL-41 (DRAK2), HD-CL-49 (nudC) and HD-CL-12 (ZNF195) for further analysis with respect to their prognostic and therapeutic value for CTCL.
|
17979976 |
2008 |