Neoplasms
|
0.090 |
AlteredExpression
|
group |
BEFREE |
We identified a downregulation of miR-1290 in ER(high) Ki67(low) tumors.
|
23183268 |
2013 |
Malignant neoplasm of breast
|
0.020 |
Biomarker
|
disease |
BEFREE |
miR-1290 and its potential targets are associated with characteristics of estrogen receptor α-positive breast cancer.
|
23183268 |
2013 |
Pancreatic carcinoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
The detection of elevated circulating miR-1290 has the potential to improve the early detection of pancreatic cancer.
|
23697990 |
2013 |
Malignant neoplasm of pancreas
|
0.020 |
Biomarker
|
disease |
BEFREE |
The detection of elevated circulating miR-1290 has the potential to improve the early detection of pancreatic cancer.
|
23697990 |
2013 |
Breast Carcinoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
miR-1290 and its potential targets are associated with characteristics of estrogen receptor α-positive breast cancer.
|
23183268 |
2013 |
Neuroendocrine Tumors
|
0.010 |
Biomarker
|
group |
BEFREE |
Of the significantly elevated circulating miRNAs in patients with pancreatic cancer compared with controls, miR-1290 had the best diagnostic performance: receiver operating characteristic (ROC) analysis on miR-1290 serum level yielded curve areas (AUC) of 0.96 [95% confidence interval (CI), 0.91-1.00], 0.81 (0.71-0.91), and 0.80 (0.67-0.93), for subjects with pancreatic cancer (n = 41) relative to healthy controls (n = 19), subjects with chronic pancreatitis (n = 35), and pancreatic neuroendocrine tumors (n = 18), respectively.
|
23697990 |
2013 |
stage, pancreatic cancer
|
0.010 |
AlteredExpression
|
phenotype |
BEFREE |
Serum miR-1290 levels distinguished patients with low-stage pancreatic cancer from controls better than CA19-9 levels, and like CA19-9, higher miR-1290 levels predicted poorer outcome among patients undergoing pancreaticoduodenectomy.
|
23697990 |
2013 |
Oestrogen receptor positive breast cancer
|
0.010 |
Biomarker
|
disease |
BEFREE |
Our results suggest that miR-1290 and its potential targets might be associated with characteristics of ER-positive breast cancer.
|
23183268 |
2013 |
Intraductal papillary mucinous neoplasm
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Serum miR-1290 levels were also significantly higher than healthy controls among patients with intraductal papillary mucinous neoplasm (IPMN; n = 20; AUC = 0.76, 0.61-0.91).
|
23697990 |
2013 |
Malignant neoplasm of breast
|
0.020 |
Biomarker
|
disease |
BEFREE |
The aim of the present study was to determine whether NAT1 is a bona fide target of miR-1290, and to investigate the impact of NAT1 on breast cancer prognosis.
|
25528056 |
2014 |
Breast Carcinoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
The aim of the present study was to determine whether NAT1 is a bona fide target of miR-1290, and to investigate the impact of NAT1 on breast cancer prognosis.
|
25528056 |
2014 |
Hamartoma Syndrome, Multiple
|
0.010 |
Biomarker
|
disease |
BEFREE |
Deregulation of seven miRNAs (miR-31-5p, miR-192-3p, miR-194-5p, miR-551a, miR-551b-5p, miR-638 and miR-1290) was determined in a larger series of CD patients with different clinical phenotypes compared with non-CD subjects.
|
24063611 |
2014 |
Neoplasms
|
0.090 |
Biomarker
|
group |
BEFREE |
Taken together, our findings suggested that miR-1290 functions as a tumor oncogene in the progression of ESCC by targeting NFIX.
|
26653554 |
2015 |
Neoplasms
|
0.090 |
AlteredExpression
|
group |
BEFREE |
Upregulation of miR-1290 was associated with tumor differentiation (P = 0.021), N classification (P = 0.006) and tumor-node-metastasis stage (P = 0.021) in ESCC patients.
|
25805931 |
2015 |
Tumor Cell Invasion
|
0.090 |
AlteredExpression
|
phenotype |
BEFREE |
Moreover, ectopic miR-1290 expression potently promoted ESCC cell growth (P < 0.01), migration (P < 0.01) and invasion (P < 0.01) in vitro. miR-1290 overexpression in ESCC cell lines decreased SCAI expression at the translational level and reduced SCAI-driven luciferase-reporter activity (P < 0.01).
|
25805931 |
2015 |
Tumor Cell Invasion
|
0.090 |
Biomarker
|
phenotype |
BEFREE |
We demonstrated that miR-1290 could promote proliferation, migration and invasion via the negative regulation of NFIX expression.
|
26653554 |
2015 |
Neoplasm Metastasis
|
0.070 |
Biomarker
|
phenotype |
BEFREE |
MicroRNA-1290 promotes esophageal squamous cell carcinoma cell proliferation and metastasis.
|
25805931 |
2015 |
Non-Small Cell Lung Carcinoma
|
0.060 |
Biomarker
|
disease |
BEFREE |
These findings provide insights into the clinical prospect of miR-1290-based therapies for non-small cell lung cancer.
|
25783528 |
2015 |
Squamous cell carcinoma of esophagus
|
0.040 |
Biomarker
|
disease |
BEFREE |
Our findings suggested that miR-1290 may play an oncogenic role in cellular processes of ESCC.
|
25805931 |
2015 |
Squamous cell carcinoma of esophagus
|
0.040 |
Biomarker
|
disease |
BEFREE |
By overexpressing or silencing miR-1290 in ESCC cells, we experimentally validated that miR-1290 directly binds to the 3'-UTR of the NFIX transcript and degrade the NFIX mRNA to regulate NFIX expression.
|
26653554 |
2015 |
Tumor Progression
|
0.020 |
Biomarker
|
phenotype |
BEFREE |
MiR-1290 promotes cancer progression by targeting nuclear factor I/X(NFIX) in esophageal squamous cell carcinoma (ESCC).
|
26653554 |
2015 |
Laryngeal Squamous Cell Carcinoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
Taken together, we propose miR-1290 as the new oncomiR involved in LSCC pathogenesis.
|
26694163 |
2015 |
Carcinoma of larynx
|
0.010 |
Biomarker
|
disease |
BEFREE |
Global miRNA Expression Profiling Identifies miR-1290 as Novel Potential oncomiR in Laryngeal Carcinoma.
|
26694163 |
2015 |
Hormone refractory prostate cancer
|
0.010 |
Biomarker
|
disease |
BEFREE |
Exosomal miR-1290 and miR-375 as prognostic markers in castration-resistant prostate cancer.
|
25129854 |
2015 |
Neoplasms
|
0.090 |
AlteredExpression
|
group |
BEFREE |
High miR-1290 expression in serum and tissue was significantly associated with tumor aggressiveness and poor prognosis.
|
27502702 |
2016 |