Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Deletion of Tet2 in murine melanoma and colon tumor cells reduced chemokine expression and TILs, enabling tumors to evade anti-tumor immunity and to resist anti-PD-L1 therapy.
|
31310587 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Tet methylcytosine dioxygenase 2 (<i>TET2</i>) is a tumor suppressor gene that is inactivated in a wide range of hematological cancers.
|
31231651 |
2019 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
Loss-of-function TET2 mutations (TET2<sup>MT</sup>) are frequent early clonal events in myeloid neoplasms and are thought to confer a fitness advantage to hematopoietic precursors.
|
31836856 |
2019 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
The proposed classification of missense TET2 variants would help to assess their clinical impact on human neoplasia and may guide future structure-and-function investigations of TET family members.
|
31187595 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Additionally, evidence was provided that TET2 regulated interleukin-6 levels in the tumor microenvironment through histone acetylation and therefore served an important role in the development of cisplatin resistance in GC cells.
|
31570278 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We retrospectively collected tumor and available matched serum samples at diagnosis and 1 and 3 months post-alloSCT from 53 patients with AML/MDS.
|
30936070 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Knockdown of TET1 or ectopic expression of TET2 in T-ALL was associated with genome-wide changes in 5mC and 5hmC enrichment and decreased cell proliferation, suggesting a tumor promoting function of TET1, and a tumor suppressing role for TET2.
|
31266538 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Utilizing a mouse model in which the loss of TET2 precedes the expression of oncogenic Kit, similar to the human disease, results in the development of a non-mast cell lineage neoplasm (AHNMD), which is responsive to PI3K inhibition.
|
29467326 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
SIGNIFICANCE: We show that TET2 is required for exit of the GC, B-cell differentiation, and is a tumor suppressor for mature B cells.
|
30274972 |
2018 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
A systematic study of serial samples from 30 patients show that ASXL1 c.1934dupG is a somatic mutation in haematological neoplasms including MDS, AML, MPN and MDS/MPN and often is associated with somatic mutations of TET2, EZH2, IDH2, RUNX1, NRAS and DNMT3A.
|
30222780 |
2018 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
AITL is characterized by loss-of-function mutations in Ten-Eleven Translocation 2 (TET2) epigenetic tumor suppressor and a highly recurrent mutation (p.Gly17Val) in the RHOA small GTPase.
|
29398449 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We found that TET2 knockout enhanced colony formation ability and in vivo tumor formation ability of MCF-7 cell, whereas TET2 depletion not affected the growth rate of MCF-7 cell in the culture.
|
30385776 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
TET2 knockdown in OS cells suppressed upregulation of IL-6 and demethylation of its promoter in xenograft tumors and decreased tumor metastasis.
|
29515232 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Increased glucose levels impede AMPK-mediated phosphorylation at serine 99, which results in the destabilization of TET2 followed by dysregulation of both 5-hydroxymethylcytosine (5hmC) and the tumour suppressive function of TET2 in vitro and in vivo.
|
30022161 |
2018 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Upregulation of TET2 in the KDM2A-depleted cells induces the re-activation of two TET downstream tumor suppressor genes, epithelial cell adhesion molecule (EpCAM) and E-cadherin, and inhibits migration and invasion.
|
28785073 |
2017 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
This resulted in increased numbers of effector T cells in the tumor, and T cell depletion abolished the reduced tumor growth observed upon myeloid-specific deletion of Tet2.
|
28813659 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Here, we show that TET2, a cellular tumor suppressor involved in active DNA demethylation, plays a central role in regulating the DNA methylation state during EBV latency.
|
28794029 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
A gene co-expression network identified using TCGA prostate tumour RNA-sequencing identifies co-regulated cancer genes associated with 2-oxoglutarate (2-OG) and succinate metabolism, including TET2, lysine demethylase (KDM) KDM6A, BRCA1-associated BAP1, and citric acid cycle enzymes IDH1/2, SDHA/B, and FH.
|
27819678 |
2017 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
The ten-eleven-translocation-2 (TET2) gene is a novel tumor suppressor gene involved in several hematological malignancies of myeloid and lymphoid origin.
|
27644645 |
2016 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
In addition to the common i(17q), these neoplasms had frequent mutations in SRSF2 (55%), SETBP1 (59%), ASXL1 (55%), and NRAS (31%); TET2 and TP53 mutations were rare.
|
26883102 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Here, we re-activated hypermethylated candidate tumor suppressor genes (TSGs) (C13ORF18, CCNA1, TFPI2, and Maspin) by TET2-induced demethylation in cervical cancer cell lines.
|
26686387 |
2016 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
We herein aimed to investigate TET2 mutations and their impact on TET2 expression in a cohort of patients with myeloid neoplasms, including MDS and AML patients.
|
26984174 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Immunohistochemistry was used to assess the levels of 5 mC, 5 hmC, TET1, and TET2 in the corresponding tumor adjacent normal (n = 309), ductal carcinoma in situ (DCIS, n = 120), and invasive ductal carcinoma (IDC, n = 309) tissues for 309 breast ductal carcinoma patients.
|
26253945 |
2015 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
TET2 functions as a bona fide tumor suppressor particularly in the pathogenesis of myeloid malignancies resembling chronic myelomonocytic leukemia (CMML) and myelodysplastic syndromes (MDS) in human.
|
25510268 |
2015 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Furthermore, decreased expression of miR-29b results in reduced tumour growth and increased TET2 expression in an animal model of HRPC.
|
26404510 |
2015 |