Malignant neoplasm of endometrium
|
0.010 |
Biomarker
|
disease |
BEFREE |
Stanniocalcin-2 May Be a Potentially Valuable Prognostic Marker in Endometrial Cancer: a Preliminary Study.
|
30661222 |
2019 |
Chronic Obstructive Airway Disease
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
The central finding of this work is that STC2 is overexpressed in COAD tissues and positively correlated with poor prognosis.
|
31236000 |
2019 |
Malignant neoplasm of lung
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Further, clinical analysis showed that STC2 expression was increased after the development of EGFR TKI resistance and that higher levels were correlated with shorter progression-free survival in EGFR TKI-treated lung cancer patients.
|
31162839 |
2019 |
Adenocarcinoma of colon
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Sp1 contributes to overexpression of stanniocalcin 2 through regulation of promoter activity in colon adenocarcinoma.
|
31236000 |
2019 |
Hypothalamic amenorrhea
|
0.010 |
Biomarker
|
disease |
BEFREE |
IGF-binding proteins (IGFBPs) and related proteases (total and intact IGFBP 3 and IGFBP 4, total IGFBP 5, PAPPA, PAPPA2 and Stanniocalcin-2), during acute (short-term fasting in healthy subjects) and chronic (women with hypothalamic amenorrhea [HA] due to excessive exercise) energy deprivation and whether metreleptin administration, in replacement, supraphysiologic or pharmacologic levels, may mediate any changes of circulating levels of the above molecules in healthy individuals and in women with hypothalamic amenorrhea.
|
31103608 |
2019 |
Endometrial Carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Stanniocalcin-2 May Be a Potentially Valuable Prognostic Marker in Endometrial Cancer: a Preliminary Study.
|
30661222 |
2019 |
Carcinoma of lung
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Further, clinical analysis showed that STC2 expression was increased after the development of EGFR TKI resistance and that higher levels were correlated with shorter progression-free survival in EGFR TKI-treated lung cancer patients.
|
31162839 |
2019 |
Primary malignant neoplasm of lung
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Further, clinical analysis showed that STC2 expression was increased after the development of EGFR TKI resistance and that higher levels were correlated with shorter progression-free survival in EGFR TKI-treated lung cancer patients.
|
31162839 |
2019 |
Nasopharyngeal carcinoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
<b>Purpose:</b> We previously demonstrated that overexpression of STC2 in nasopharyngeal carcinomas (NPC) positively correlates with radiation resistance and tumor metastasis, two major clinical obstacles to the improvement of NPC management.
|
31372045 |
2019 |
Oestrogen receptor positive breast cancer
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
The expression level of STC2 gene was significantly higher in estrogen receptor (ER) positive breast cancer tissues than in ER negative ones (P<0.001).
|
31845230 |
2019 |
Luminal A Breast Carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Based on the immunohistochemical detection of CDCA8, BCL2 and STC2, we identified a luminal A-like subgroup of TPBCs in the FUSCC cohort (CDCA8-negative, BCL2- and/or STC2-positive).
|
31410192 |
2019 |
Anemia of chronic disease
|
0.010 |
Biomarker
|
phenotype |
BEFREE |
Together, these findings newly identify STC2 as the first stanniocalcin responsible for mediating the immunomodulatory effects of MSCs on allogeneic T cells and STC2 contribute to MSC-based treatment for ACD mainly via reducing the CD8<sup>+</sup> Tc1 cells.
|
29748538 |
2018 |
Rectal Carcinoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Tumors with high mRNA levels of STC2 were more common in patients with rectal cancer, left-sided CRC, advanced T-stage (T3-T4), positive lymph node involvement and advanced AJCC-stage (III-IV) from TCGA.
|
30425508 |
2018 |
Diabetes Mellitus
|
0.010 |
Biomarker
|
group |
BEFREE |
Summarizing, we present evidence of the role of STCs, mainly STC2, as a possible early marker during development of diabetes mellitus.
|
28990324 |
2018 |
Fatty Liver
|
0.010 |
Biomarker
|
disease |
BEFREE |
Together, our results revealed an important role of STC2 in the regulation of hepatic triglyceride metabolism, which might provide a potential therapeutic target for the treatment of fatty liver and related metabolic disorders.
|
30038584 |
2018 |
Glioblastoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
MiR-184 was under-expressed whereas STC2 was over-expressed in glioblastoma tissues and cell line.
|
28887636 |
2018 |
Heart failure
|
0.010 |
Biomarker
|
disease |
BEFREE |
In STEMI patients, Stanniocalcin-2 and IGFBP-4 emerged as independent predictors of all-cause death and readmission due to HF.
|
29712555 |
2018 |
Congestive heart failure
|
0.010 |
Biomarker
|
disease |
BEFREE |
In STEMI patients, Stanniocalcin-2 and IGFBP-4 emerged as independent predictors of all-cause death and readmission due to HF.
|
29712555 |
2018 |
Hypertriglyceridemia
|
0.010 |
AlteredExpression
|
phenotype |
BEFREE |
Systemic administration of STC2 recombinant protein or adenovirus-mediated overexpression of STC2 markedly attenuated hepatosteatosis and hypertriglyceridemia in obese mice.
|
30038584 |
2018 |
Metabolic Diseases
|
0.010 |
Biomarker
|
group |
BEFREE |
Together, our results revealed an important role of STC2 in the regulation of hepatic triglyceride metabolism, which might provide a potential therapeutic target for the treatment of fatty liver and related metabolic disorders.
|
30038584 |
2018 |
Adult Glioblastoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
MiR-184 was under-expressed whereas STC2 was over-expressed in glioblastoma tissues and cell line.
|
28887636 |
2018 |
Childhood Glioblastoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
MiR-184 was under-expressed whereas STC2 was over-expressed in glioblastoma tissues and cell line.
|
28887636 |
2018 |
Avellino corneal dystrophy
|
0.010 |
Biomarker
|
disease |
BEFREE |
Together, these findings newly identify STC2 as the first stanniocalcin responsible for mediating the immunomodulatory effects of MSCs on allogeneic T cells and STC2 contribute to MSC-based treatment for ACD mainly via reducing the CD8<sup>+</sup> Tc1 cells.
|
29748538 |
2018 |
ST segment elevation myocardial infarction
|
0.010 |
Biomarker
|
disease |
BEFREE |
The Stanniocalcin-2/PAPP-A/IGFBP-4 axis exhibits a significant role in STEMI risk stratification.
|
29712555 |
2018 |
Glioblastoma Multiforme
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
MiR-184 was under-expressed whereas STC2 was over-expressed in glioblastoma tissues and cell line.
|
28887636 |
2018 |