Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
The role of STAG2 in gene regulation, hematopoiesis, and tumor suppression remains unresolved.
|
31495782 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In the progressor-enriched Aarhus cohort, 38% of tumors with intact STAG2 expression progressed within 5 years, versus 16% of STAG2-deficient tumors (<i>P</i> < 0.01).
|
29954776 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Collectively, these data suggest that STAG2 acts as a tumor suppressor gene in bladder cancer and may be a potential therapeutic target in BC.
|
28627627 |
2017 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
When activated, STAG2 may act as a 'caretaker' tumor suppressor gene.
|
28352327 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Here we show that the loss-of-function of STAG2, a core component of cohesin and an emerging tumour suppressor, leads to synthetic dependency of mutated cancer cells on its paralog STAG1.
|
28430577 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Loss of STAG2 was significantly correlated with histological low grade, papillary architecture, noninvasive tumors, absence of concomitant carcinoma in situ, and lower Ki-67 expression.
|
28967037 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
However, studies of naturally occurring human tumors have demonstrated little, if any, correlation between STAG2 mutational status and aneuploidy, and have further shown that STAG2-deficient tumors are often euploid.
|
26871722 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Our studies unveil a previously unknown genetic mechanism of BRAFi resistance and provide new insights into the tumor suppressor function of STAG2 and STAG3.
|
27500726 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Strikingly, ectopic expression of miR-409 in normal prostate fibroblasts conferred a cancer-associated stroma-like phenotype and led to the release of miR-409 via extracellular vesicles to promote tumor induction and epithelial-to-mesenchymal transition in vitro and in vivo. miR-409 promoted tumorigenesis through repression of tumor suppressor genes such as Ras suppressor 1 and stromal antigen 2.
|
25065597 |
2015 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
STAG2 depletion leads to loss of centromere cohesion in vitro, and some human neoplasms have been shown to lose expression of this protein.
|
24822266 |
2014 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
Mutations in the STAG2 gene are present in ∼20% of tumors from different tissues of origin.
|
25074805 |
2014 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
Using a combination of whole genome sequencing and targeted sequencing approaches, we discover that EFT has a very low mutational burden (0.15 mutations/Mb) but frequent deleterious mutations in the cohesin complex subunit STAG2 (21.5% tumors, 44.4% cell lines), homozygous deletion of CDKN2A (13.8% and 50%) and mutations of TP53 (6.2% and 71.9%).
|
25010205 |
2014 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
However, we discovered that loss of STAG2 expression occurs in 15% of tumors and is associated with metastatic disease, suggesting a potential genetic vulnerability in Ewing sarcoma.
|
25186949 |
2014 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
We further tested STAG2 expression in gastric adenocarcinomas and glioblastomas, as these tumor types were previously shown to lose STAG2 expression.
|
24318971 |
2014 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Finally, we detected subclonal STAG2 mutations in diagnostic tumors and expansion of STAG2-immunonegative cells in relapsed tumors as compared with matched diagnostic samples.
|
25223734 |
2014 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
As the genetic contribution to aneuploidy is unknown in NB, we investigated the presence of STAG2 mutations through sequence analysis of all 33 coding exons in 37 primary NB tumors.
|
24088605 |
2013 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Our findings indicate that STAG2 is a new UBC tumor suppressor acting through mechanisms that are different from its role in preventing aneuploidy.
|
24121791 |
2013 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
A diverse range of tumor types were found to harbor deletions or inactivating mutations of STAG2, a gene encoding a subunit of the cohesin complex, which regulates the separation of sister chromatids during cell division.
|
21852505 |
2011 |