Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
The SET domain‑containing 1B (SETD1B) gene is involved in multiple biological processes, including tumor development and progression.
|
30628696 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Further exploration of tumor sequence data from TCGA predicts the presence of MLL1 fusions with truncated SET domain in prostate tumors.
|
30548174 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
TCGA data revealed upregulation of SET and CIP2A and positive correlation of these two gene expressions in TNBC tumors.
|
30651219 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Protein phosphatase 2A (PP2A), a tumor suppressor, has been shown to be downregulated in many human cancers via multiple mechanisms including upregulation of its endogenous inhibitors, I2PP2A or CIP2A.
|
30286326 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Here, it was determined that SET expression was elevated in tumor tissue in a gastric cancer mouse model system, and SET expression was positively correlated with poor survival of human gastric cancer patients.
|
29330298 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
The histone methyltransferase multiple myeloma SET domain protein (MMSET/WHSC1) is highly expressed in diverse tumor types, and its expression appears to be involved in cell proliferation.
|
30013191 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
<i>In vivo</i>, SET isoform 2 overexpression significantly correlated with increased N-cadherin in human PDAC and to tumor burden and metastatic ability in an orthotopic mouse tumor model.
|
28978088 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Here, we investigated the role of SET in the tumorigenic growth in canine mammary tumor as well as in the sensitivity of tumors to existing therapeutics.
|
28655918 |
2017 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Altogether, our results show that miR-199b is a tumor suppressor whose downregulation independently determines worse outcome and emerges as a potential contributing mechanism to inhibit PP2A via SET overexpression in a subgroup of mCRC patients.
|
27517624 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Several, cell signaling mechanisms involved in tumor pathogenesis have been identified, leading to the production of new tumor markers and to set targets for therapy, including cytokines, enzymes, proteantigens.
|
28356044 |
2017 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Overexpression of SET has been characterized as being tumor-specific and is associated with adverse clinical outcomes in many different human malignant diseases.
|
28548025 |
2017 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Recent evidence suggests that inhibition of protein phosphatase 2A (PP2A) tumor suppressor activity via the SET oncoprotein contributes to the pathogenesis of various cancers.
|
27705940 |
2016 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
By analyzing samples obtained from 147 HCC patients, we found that SET overexpression was detected specifically in 30.6% HCC tumor samples, and was significantly associated with worse clinical features and high p-Akt expression in HCC tumors.
|
26876205 |
2016 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Furthermore, parallel immunohistochemical analysis of three PP2A inhibitors demonstrated that two PP2A inhibitors, CIP2A and SET, are highly expressed in both dysplastic and adenocarcinomatous tumors of the Smgb-Tag mice.
|
26395031 |
2016 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Mechanistic studies identified SET as a direct target of miR-125b, and the downregulation of SET, observed during tumor migration, was affected by the overexpression of miR125b.
|
27383536 |
2016 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
In addition, knocking-down SET expression decreases tumor cell sensitivity to TGI1002.
|
25900240 |
2015 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
STIC was significantly more frequent in tumors from the BRCA cohort (66% vs. 31%, P=0.017) and specifically the BRCA tumors with classic morphology (83%) versus those with SET morphology (22%, P=0.003).
|
25581732 |
2015 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
SET could promote the occurrence of tumor through inhibiting PP2A.
|
25234598 |
2014 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
SET is known to be an inhibitor of phosphatase 2A (PP2A), which functions as a tumor suppressor by inhibiting the signal transduction pathway and inducing apoptosis.
|
24621013 |
2014 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
SET domain-containing proteins such as MLL1 play a critical role in leukemogenesis, while others such as SETD2 may function as a tumor suppressor in breast cancer and renal cell carcinoma.
|
23065515 |
2013 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We show here that the tumour suppressor ceramide binds I2PP2A/SET selectively in the nucleus and including its K209 and Y122 residues as determined by molecular modelling/simulations and site-directed mutagenesis.
|
23180565 |
2013 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
The tumour suppressor and chromatin-remodelling factor BRG1 antagonizes Myc activity and promotes cell differentiation in human cancer.
|
22407764 |
2012 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
The chromatin remodelling factor BRG1 is a novel binding partner of the tumor suppressor p16INK4a.
|
19149898 |
2009 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Intact PR or SET sequence is required for tumor suppression functions, but it remains unclear whether it is histone methyltransferase activity that underlies tumor suppression.
|
14633678 |
2003 |