Malignant neoplasm of breast
|
0.380 |
AlteredExpression
|
disease |
BEFREE |
WITHDRAWN: Downregulation of MicroRNA-152 and Inhibition of Cell Proliferation, Migration, and Invasion in Breast Cancer.
|
28653610 |
2017 |
Breast Carcinoma
|
0.380 |
AlteredExpression
|
disease |
BEFREE |
WITHDRAWN: Downregulation of MicroRNA-152 and Inhibition of Cell Proliferation, Migration, and Invasion in Breast Cancer.
|
28653610 |
2017 |
Tumor Cell Invasion
|
0.100 |
AlteredExpression
|
phenotype |
BEFREE |
WITHDRAWN: Downregulation of MicroRNA-152 and Inhibition of Cell Proliferation, Migration, and Invasion in Breast Cancer.
|
28653610 |
2017 |
Tumor Cell Invasion
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
When miR-152 was enhanced, the invasion and migration of NPC cells were inhibited.
|
29628766 |
2018 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
We validated 12 miRNAs implicated in tumor development using primary STS samples and selected miR-152 for further analysis in STS-derived cell lines.
|
27900663 |
2017 |
Diabetes Mellitus, Insulin-Dependent
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
We observed strong evidence for the association of hsa-miR-152-3p plasma levels and DN in patients with T2D, confirming an association previously observed in patients with type 1 diabetes.
|
29361146 |
2018 |
Diabetes Mellitus, Non-Insulin-Dependent
|
0.030 |
AlteredExpression
|
disease |
BEFREE |
We observed strong evidence for the association of hsa-miR-152-3p plasma levels and DN in patients with T2D, confirming an association previously observed in patients with type 1 diabetes.
|
29361146 |
2018 |
Diabetic Nephropathy
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
We observed strong evidence for the association of hsa-miR-152-3p plasma levels and DN in patients with T2D, confirming an association previously observed in patients with type 1 diabetes.
|
29361146 |
2018 |
Carcinogenesis
|
0.060 |
PosttranslationalModification
|
phenotype |
BEFREE |
We identified E2F3, MET, and Rictor as novel candidate targets of miR-152, suggesting how its epigenetic silencing can drive endometrial carcinogenesis.
|
21868754 |
2011 |
Multiple Myeloma
|
0.040 |
Biomarker
|
disease |
BEFREE |
We further characterized the hypermethylation-dependent inhibition of miR-152, -10b-5p and -34c-3p which was shown to exert a putative tumor suppressive role in MM.
|
25330074 |
2014 |
Multiple Myeloma
|
0.040 |
AlteredExpression
|
disease |
BEFREE |
We found that target genes of the most differentially expressed miRNAs are directly involved in the pathogenesis of MM; specifically, the inhibition of hsa-miR-425, hsa-miR-152 and hsa-miR-24, which are all downregulated in h-MM, leads to the overexpression of CCND1, TACC3, MAFB, FGFR3 and MYC, which are the also the oncogenes upregulated by the most frequent IgH chromosomal translocations occurring in nh-MM.
|
23174883 |
2013 |
Multiple Myeloma
|
0.040 |
AlteredExpression
|
disease |
BEFREE |
We found that levels of H19 and BRD4 were up-regulated, and the expression of miR-152-3p was down-regulated in MM patients.
|
31712391 |
2020 |
Hepatocarcinogenesis
|
0.040 |
Biomarker
|
disease |
BEFREE |
We found that dysregulation of MIR7 contributes to the initiation and progression of inflammation-induced gastric cancer; dysregulation of MIR9 contributes to HIV-1 infection to hijack CD4+ T cells through dysfunction of the immune and hormone pathways; dysregulation of MIR139-5p, MIRLET7i, and MIR10a contributes to the HIV-1 integration/replication stage; dysregulation of MIR101, MIR141, and MIR152 contributes to the HIV-1 virus assembly and budding mechanisms; dysregulation of MIR302a contributes to not only microvesicle-mediated transfer of miRNAs but also dysfunction of NF-κB signaling pathway in hepatocarcinogenesis.
|
26897165 |
2016 |
Immunologic Deficiency Syndromes
|
0.010 |
Biomarker
|
group |
BEFREE |
We found that dysregulation of MIR7 contributes to the initiation and progression of inflammation-induced gastric cancer; dysregulation of MIR9 contributes to HIV-1 infection to hijack CD4+ T cells through dysfunction of the immune and hormone pathways; dysregulation of MIR139-5p, MIRLET7i, and MIR10a contributes to the HIV-1 integration/replication stage; dysregulation of MIR101, MIR141, and MIR152 contributes to the HIV-1 virus assembly and budding mechanisms; dysregulation of MIR302a contributes to not only microvesicle-mediated transfer of miRNAs but also dysfunction of NF-κB signaling pathway in hepatocarcinogenesis.
|
26897165 |
2016 |
HIV-1 infection
|
0.010 |
Biomarker
|
disease |
BEFREE |
We found that dysregulation of MIR7 contributes to the initiation and progression of inflammation-induced gastric cancer; dysregulation of MIR9 contributes to HIV-1 infection to hijack CD4+ T cells through dysfunction of the immune and hormone pathways; dysregulation of MIR139-5p, MIRLET7i, and MIR10a contributes to the HIV-1 integration/replication stage; dysregulation of MIR101, MIR141, and MIR152 contributes to the HIV-1 virus assembly and budding mechanisms; dysregulation of MIR302a contributes to not only microvesicle-mediated transfer of miRNAs but also dysfunction of NF-κB signaling pathway in hepatocarcinogenesis.
|
26897165 |
2016 |
Malignant neoplasm of prostate
|
0.060 |
AlteredExpression
|
disease |
BEFREE |
We found that miR-152-3p was underexpressed in PCa and that lower expression levels were associated with promoter hypermethylation in accordance with TCGA dataset analysis.
|
29599847 |
2018 |
Prostate carcinoma
|
0.060 |
AlteredExpression
|
disease |
BEFREE |
We found that miR-152-3p was underexpressed in PCa and that lower expression levels were associated with promoter hypermethylation in accordance with TCGA dataset analysis.
|
29599847 |
2018 |
Liver carcinoma
|
0.090 |
AlteredExpression
|
disease |
BEFREE |
We found higher signals for miR-122 and miR-152 in non-tumor liver and HCC tissues compared to control tissues.
|
28512857 |
2018 |
melanoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
We determined that HOTAIR acts as a ceRNA to promote malignant melanoma progression by sponging miR-152-3p.
|
29156728 |
2017 |
Osteosarcoma
|
0.040 |
Biomarker
|
disease |
BEFREE |
We demonstrated that microRNA‑152 inhibits cell proliferation of osteosarcoma through DKK1 by directly targeting Wnt/β‑catenin signaling pathway.
|
29845282 |
2018 |
Osteosarcoma of bone
|
0.040 |
Biomarker
|
disease |
BEFREE |
We demonstrated that microRNA‑152 inhibits cell proliferation of osteosarcoma through DKK1 by directly targeting Wnt/β‑catenin signaling pathway.
|
29845282 |
2018 |
Childhood Osteosarcoma
|
0.040 |
Biomarker
|
disease |
BEFREE |
We demonstrated that microRNA‑152 inhibits cell proliferation of osteosarcoma through DKK1 by directly targeting Wnt/β‑catenin signaling pathway.
|
29845282 |
2018 |
Neoplasm Metastasis
|
0.060 |
Biomarker
|
phenotype |
BEFREE |
We also investigated and confirmed the role of miR-152-5p in GC by a series of experiments, and found that miR-152-5p modulated cell viability, migration, invasion, and cell-cycle progression of human GC cells, and also inhibited tumor growth and metastasis <i>in vivo</i> partially by targeting PIK3CA.
|
29904279 |
2018 |
Malignant neoplasm of stomach
|
0.080 |
Biomarker
|
disease |
BEFREE |
We also investigated and confirmed the role of miR-152-5p in GC by a series of experiments, and found that miR-152-5p modulated cell viability, migration, invasion, and cell-cycle progression of human GC cells, and also inhibited tumor growth and metastasis <i>in vivo</i> partially by targeting PIK3CA.
|
29904279 |
2018 |
Stomach Carcinoma
|
0.080 |
Biomarker
|
disease |
BEFREE |
We also investigated and confirmed the role of miR-152-5p in GC by a series of experiments, and found that miR-152-5p modulated cell viability, migration, invasion, and cell-cycle progression of human GC cells, and also inhibited tumor growth and metastasis <i>in vivo</i> partially by targeting PIK3CA.
|
29904279 |
2018 |