Hepatitis, Toxic
|
0.300 |
Biomarker
|
disease |
CTD_human |
"Serum microRNA signatures as ""liquid biopsies"" for interrogating hepatotoxic mechanisms and liver pathogenesis in human."
|
28545106 |
2017 |
Drug-Induced Liver Disease
|
0.300 |
Biomarker
|
phenotype |
CTD_human |
"Serum microRNA signatures as ""liquid biopsies"" for interrogating hepatotoxic mechanisms and liver pathogenesis in human."
|
28545106 |
2017 |
Hepatitis, Drug-Induced
|
0.300 |
Biomarker
|
disease |
CTD_human |
"Serum microRNA signatures as ""liquid biopsies"" for interrogating hepatotoxic mechanisms and liver pathogenesis in human."
|
28545106 |
2017 |
Drug-Induced Acute Liver Injury
|
0.300 |
Biomarker
|
disease |
CTD_human |
"Serum microRNA signatures as ""liquid biopsies"" for interrogating hepatotoxic mechanisms and liver pathogenesis in human."
|
28545106 |
2017 |
Chemical and Drug Induced Liver Injury
|
0.300 |
Biomarker
|
disease |
CTD_human |
"Serum microRNA signatures as ""liquid biopsies"" for interrogating hepatotoxic mechanisms and liver pathogenesis in human."
|
28545106 |
2017 |
Chemically-Induced Liver Toxicity
|
0.300 |
Biomarker
|
disease |
CTD_human |
"Serum microRNA signatures as ""liquid biopsies"" for interrogating hepatotoxic mechanisms and liver pathogenesis in human."
|
28545106 |
2017 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
MiR-574-5p induces microsomal prostaglandin E synthase-1 (mPGES-1) expression by preventing CUGBP1 binding to its 3'UTR, leading to an enhanced alternative splicing and generation of an mPGES-1 3'UTR isoform, increased mPGES-1 protein expression, PGE<sub>2</sub> formation, and tumor growth <i>in vivo.</i> miR-574-5p-induced tumor growth in mice could be completely inhibited with the mPGES-1 inhibitor CIII.
|
30922080 |
2019 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
MiR-574-3p functioned as a tumor suppressor in OC, which might be served as a potential target for the diagnosis and therapy for OC.
|
31486483 |
2019 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Positive PD-L1 expression on tumor cells was associated with advanced stages (P = 0.041) and TILs infiltration (P = 0.005), whereas decreased miR-574-3p level correlated with higher muscle invasion (P = 0.012), more severe tumor necrosis (P = 0.022) and poor patient survival.
|
29051990 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Further studies suggested that LOC101927497 may function as a tumor suppressor by interacting with miR-574-5p.
|
29223541 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Overall, the results of the present study highlighted the potential tumour inhibitory roles of miR‑574 in GBM, thereby indicating that miR‑574 may be a novel and efficient therapeutic target for the treatment of patients with GBM.
|
29901177 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Nude mouse tumorigenicity assay was used to study the effect of inhibiting miR-574-5p on development and tumorigenic ability of Henrietta Lacks (HeLa) tumor.
|
27049079 |
2016 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Expression of miR-574-5p, Qki5/6/7/7b splicing variants, β-catenin and p27(Kip1) was determined in mouse and human CRC cells and tissues to investigate the post-transcriptional regulation of Qki isoforms by miR-574-5p and its impact on β-catenin/p27(Kip1) signalling, cell cycle progression, proliferation, migration, invasion and tumour growth.
|
22490519 |
2013 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Low expression level of miR-574-3p was correlated with advanced tumor stage and higher Gleason score in PCa specimens.
|
23554959 |
2013 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We are the first to demonstrate that miR-574-3p is a miRNA with tumor suppressor function and that MESDC1 (which has a potential oncogenic function in BC) may be targeted by miR-574-3p.
|
22179486 |
2012 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Thus, these data suggest that the HDAC1/miR-574-5p axis might provide a novel therapeutic target to reconstitute tumour suppressor CerS1/ceramide signalling.
|
22180294 |
2012 |
Tumor Cell Invasion
|
0.090 |
Biomarker
|
phenotype |
BEFREE |
We investigated the mechanism via which miR-574-3p regulated cancer cell migration and invasion to determine the relationship between epithelial mesenchymal transition (EMT) and drug resistance.
|
30917930 |
2019 |
Tumor Cell Invasion
|
0.090 |
Biomarker
|
phenotype |
BEFREE |
Both MFI2-AS1 siRNA and miR-574-5p mimics inhibited proliferation, migration and invasion in LoVo and RKO cells.
|
31094023 |
2019 |
Tumor Cell Invasion
|
0.090 |
AlteredExpression
|
phenotype |
BEFREE |
Beyond that, miR-574-5p was upregulated in CRC tissues, and as an oncogene, it accelerated CRC cell migration and invasion.
|
31104316 |
2019 |
Tumor Cell Invasion
|
0.090 |
AlteredExpression
|
phenotype |
BEFREE |
Functional experiments indicated that restored expression of miR‑574 using mimics led to the inhibition of the cell proliferation and invasion of GBM cells, as determined by Cell Counting kit‑8 and Matrigel invasion assays, respectively.
|
29901177 |
2018 |
Tumor Cell Invasion
|
0.090 |
AlteredExpression
|
phenotype |
BEFREE |
Positive PD-L1 expression on tumor cells was associated with advanced stages (P = 0.041) and TILs infiltration (P = 0.005), whereas decreased miR-574-3p level correlated with higher muscle invasion (P = 0.012), more severe tumor necrosis (P = 0.022) and poor patient survival.
|
29051990 |
2018 |
Tumor Cell Invasion
|
0.090 |
Biomarker
|
phenotype |
BEFREE |
Re-expression of miR-574-3p in PCa cells significantly inhibited cell proliferation, migration and invasion in vitro and in vivo. miR-574-3p restoration induced apoptosis through reducing Bcl-xL and activating caspase-9 and caspase-3.
|
23554959 |
2013 |
Tumor Cell Invasion
|
0.090 |
AlteredExpression
|
phenotype |
BEFREE |
In mouse and human CRC cells, miR-574-5p was shown to regulate Qki isoforms (Qki6/7 in particular) post-transcriptionally and caused altered expression in β-catenin and p27(Kip1) , increased proliferation, migration and invasion and decreased differentiation and cell cycle exit.
|
22490519 |
2013 |
Tumor Cell Invasion
|
0.090 |
Biomarker
|
phenotype |
BEFREE |
Gain-of-function analysis revealed that cell proliferation, migration and invasion were significantly inhibited in miR‑574‑3p-transfected BC cell lines.
|
22179486 |
2012 |
Tumor Cell Invasion
|
0.090 |
Biomarker
|
phenotype |
BEFREE |
Functional study revealed that cell proliferation, migration and invasion were significantly inhibited in miR-574-3p-transfected gastric cancer SGC7901 cells.
|
22683180 |
2012 |