Schizophrenia
|
0.400 |
Biomarker
|
disease |
BEFREE |
WBP1L is a target of microRNA 137 (miR-137) and has been considered a candidate gene for schizophrenia (SCZ).
|
31840934 |
2020 |
Squamous cell carcinoma of the head and neck
|
0.040 |
AlteredExpression
|
disease |
BEFREE |
Using both in vivo and in vitro models, we found that knocking down ASCT2 by shRNAs or miR-137 or the combination of silencing ASCT2 and pharmacologically inhibiting SNAT2 via a small-molecule antagonist called V-9302 significantly suppressed intracellular glutamine levels and downstream glutamine metabolism, including glutathione production; these effects attenuated growth and proliferation, increased apoptosis and autophagy, and increased oxidative stress and mTORC1 pathway suppression in HNSCC.
|
31819178 |
2020 |
Schizophrenia
|
0.400 |
AlteredExpression
|
disease |
BEFREE |
These results suggest that overexpression of miR-137 in the whole brain induces the several phenotypes that are relevant to aspects of psychiatric disorders, such as schizophrenia.
|
31361772 |
2019 |
Schizophrenia
|
0.400 |
AlteredExpression
|
disease |
BEFREE |
Defective regulation of miR-137 is associated with psychiatric disorders that include schizophrenia and bipolar disorder.
|
31200102 |
2019 |
Schizophrenia
|
0.400 |
Biomarker
|
disease |
BEFREE |
To evaluate the additive effects of the MIR137 regulated genes (N = 1274), we calculated a MIR137 polygenic risk score (PRS) for schizophrenia and tested its association with the risk for schizophrenia in the genomic data of a Han Chinese population that included schizophrenia patients (N = 589) and normal controls (N = 575).
|
31239006 |
2019 |
Schizophrenia
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
Our meta-analysis found that the Rs1625579 polymorphism in the MIR137 gene was associated with the risk of schizophrenia.
|
31586698 |
2019 |
Schizophrenia
|
0.400 |
GeneticVariation
|
disease |
BEFREE |
A VNTR Regulates miR-137 Expression Through Novel Alternative Splicing and Contributes to Risk for Schizophrenia.
|
31409837 |
2019 |
Bipolar Disorder
|
0.350 |
AlteredExpression
|
disease |
BEFREE |
Defective regulation of miR-137 is associated with psychiatric disorders that include schizophrenia and bipolar disorder.
|
31200102 |
2019 |
Malignant Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Analysis of the differentially expressed micro RNAs (miRNAs) between cancer and noncancer tissues reconfirmed miR-137 to be among the most relevant prognostic miRNAs and the data of 375 HCC patients and 50 normal cases were from the Cancer Genome Atlas (TCGA) data sets.
|
30523640 |
2019 |
Non-Small Cell Lung Carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
Most importantly, the complex combines the inhibitory function of the GL21.T aptamer and miR-137, leading to a negative impact on NSCLC migration and growth.
|
31276956 |
2019 |
Colorectal Carcinoma
|
0.100 |
PosttranslationalModification
|
disease |
BEFREE |
Expressions of SNHG1 and miR-137 in CRC tissues and cell lines were evaluated by quantitative real-time polymerase chain reaction.
|
31469189 |
2019 |
Glioblastoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
Antagonism between the RNA-binding protein Musashi1 and miR-137 and its potential impact on neurogenesis and glioblastoma development.
|
31004009 |
2019 |
Neoplasm Metastasis
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
In vitro experiments validated that miR-137 could bind to 3'-untranslated region of the AFM and promote the invasion and metastasis of HCC cell lines.
|
30523640 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Our data suggest that miR-137 possesses a tumor invasive suppressor function with a prognostic value in prolactinomas by targeting MITF and modulating Wnt-β-catenin signaling pathway.
|
31162548 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In gliomas, miR-137 functions as a tumor suppressor while Msi1 is a prooncogenic factor.
|
31004009 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
In addition, miR-137 expression in tumor tissues was negatively correlated with ZFPM2-AS1 expression.
|
31298319 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We found that the tumor suppressor miRNA miR-137 silenced signaling in a spectrum of human cancers and selectively targeted tripartite motif-containing 24 (TRIM24) to suppress tumor proliferation.
|
31217891 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Furthermore, miR-137 could inhibit tumor development and arrest cell cycle at the G0/G1 phase by targeting the 3'-UTR of EPS8.
|
30203615 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Moreover, the increased miR-137 heightened the sensitivity of BC cells-derived tumors to DOX through targeting DUSP4 in vivo.
|
31801953 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We show that a top-ranked miR-137 candidate gene, <i>Sorl1</i>, has a tumor suppressor function in primary PanNETs.
|
31704767 |
2019 |
Neoplasms
|
0.100 |
GeneticVariation
|
group |
BEFREE |
After adjustment for age and sex, miR-181b was associated with an increased risk of bearing BRAFV600E mutation (OR: 1.27; 95% CI: 1.01-1.61; P = 0.045) and risk of lymphovascular invasion (OR: 1.66; 95% CI: 1.01-2.72; P = 0.045); miR-137 was associated with the risk of larger tumor size (OR: 1.31; 95% CI: 1.04-1.65; P = 0.022); miR-222 was related to increase in extracapsular invasion (OR: 1.28; 95% CI: 1.04-1.57; P = 0.018).
|
30890403 |
2019 |
Adult Glioblastoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
Antagonism between the RNA-binding protein Musashi1 and miR-137 and its potential impact on neurogenesis and glioblastoma development.
|
31004009 |
2019 |
Childhood Glioblastoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
Antagonism between the RNA-binding protein Musashi1 and miR-137 and its potential impact on neurogenesis and glioblastoma development.
|
31004009 |
2019 |
Carcinogenesis
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
The overexpressed miR-137 was found to inhibit EMT, cell proliferation, colony formation, invasion, migration and tumorigenesis in nude mice.
|
31143092 |
2019 |
Tumor Cell Invasion
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
The luciferase reporter assay revealed direct binding of miR-137 to the 3'-UTR of <i>Del-1</i>. miR-137 inhibited cell proliferation, migration, and invasion of MDA-MB-231 cells.
|
31817673 |
2019 |