Malignant neoplasm of urinary bladder
|
0.020 |
Biomarker
|
disease |
BEFREE |
The significance and diagnostic usefulness of this methodology is reflected by the finding that the RNA ratio of microRNA-126:microRNA-152 enabled the detection of BCa from urine at a specificity of 82% and a sensitivity of 72%, with an area under the curve of 0.768 (95% confidence interval, 0.605-0.931).
|
19375957 |
2011 |
Bladder Neoplasm
|
0.020 |
Biomarker
|
disease |
BEFREE |
The significance and diagnostic usefulness of this methodology is reflected by the finding that the RNA ratio of microRNA-126:microRNA-152 enabled the detection of BCa from urine at a specificity of 82% and a sensitivity of 72%, with an area under the curve of 0.768 (95% confidence interval, 0.605-0.931).
|
19375957 |
2011 |
Carcinoma of bladder
|
0.020 |
Biomarker
|
disease |
BEFREE |
The significance and diagnostic usefulness of this methodology is reflected by the finding that the RNA ratio of microRNA-126:microRNA-152 enabled the detection of BCa from urine at a specificity of 82% and a sensitivity of 72%, with an area under the curve of 0.768 (95% confidence interval, 0.605-0.931).
|
19375957 |
2011 |
Carcinogenesis
|
0.060 |
Biomarker
|
phenotype |
BEFREE |
These data indicate that IL-6 can regulate the activity of DNMT-1 and expression of methylation-dependent tumor suppressor genes by modulation of miR-148a and miR-152, and provide a link between this inflammation-associated cytokine and oncogenesis in cholangiocarcinoma.
|
20146264 |
2010 |
Cholangiocarcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
These data indicate that IL-6 can regulate the activity of DNMT-1 and expression of methylation-dependent tumor suppressor genes by modulation of miR-148a and miR-152, and provide a link between this inflammation-associated cytokine and oncogenesis in cholangiocarcinoma.
|
20146264 |
2010 |
Malignant Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Expression levels of miR-148a and miR-152 in human gastric (p < 0.001 and p = 0.038, respectively, t-test) and colorectal (all p < 0.001) cancers were significantly lower than that in their matched nontumor adjacent tissues.
|
20422307 |
2010 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Furthermore, low expression of miR-152 was correlated with increased tumor size (p = 0.023 and 0.004, respectively, Mann-Whitney U test) and advanced pT stage (p = 0.018 and 0.002, respectively) in gastrointestinal cancers.
|
20422307 |
2010 |
Carcinogenesis
|
0.060 |
Biomarker
|
phenotype |
BEFREE |
MiR-148a and miR-152 may be involved in the carcinogenesis of gastrointestinal cancers and might be potential biomarkers in these cancers.
|
20422307 |
2010 |
Malignant neoplasm of gastrointestinal tract
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
Furthermore, low expression of miR-152 was correlated with increased tumor size (p = 0.023 and 0.004, respectively, Mann-Whitney U test) and advanced pT stage (p = 0.018 and 0.002, respectively) in gastrointestinal cancers.
|
20422307 |
2010 |
Tumor Cell Invasion
|
0.100 |
AlteredExpression
|
phenotype |
BEFREE |
Functional genomic experiments through enforced expression of MIR200B and knockdown of MIR152 resulted in a significant decrease of the invasion activity of SH-SY5Y cells.
|
20574809 |
2010 |
Neoplasms
|
0.100 |
PosttranslationalModification
|
group |
BEFREE |
This in turn led to a decrease in global DNA methylation, whereas inhibition of miR-152 caused global DNA hypermethylation and increased the methylation levels of two tumor suppressor genes, glutathione S-transferase pi 1 (GSTP1) and E-cadherin 1 (CDH1).
|
20578129 |
2010 |
Liver carcinoma
|
0.090 |
Biomarker
|
disease |
BEFREE |
These findings support a tumor-suppressive role of miR-152 in the epigenetic aberration of HBV-related HCC and the potential development of miRNA-based targeted approaches for the treatment of HBV-related HCC.
|
20578129 |
2010 |
Hepatitis B Virus-Related Hepatocellular Carcinoma
|
0.010 |
PosttranslationalModification
|
disease |
BEFREE |
Down-regulated microRNA-152 induces aberrant DNA methylation in hepatitis B virus-related hepatocellular carcinoma by targeting DNA methyltransferase 1.
|
20578129 |
2010 |
Malignant neoplasm of gastrointestinal tract
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
Our previous studies have revealed that miR-148a and miR-152 are significantly down-regulated in gastrointestinal cancers.
|
21205300 |
2011 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
In particular, hypermethylation at miR-148a and miR-152 was associated with microsatellite-unstable (as opposed to stable) tumors and hypermethylation at miR-18b with sporadic disease (as opposed to Lynch syndrome).
|
21327300 |
2011 |
Hereditary Nonpolyposis Colorectal Cancer
|
0.010 |
Biomarker
|
disease |
BEFREE |
In particular, hypermethylation at miR-148a and miR-152 was associated with microsatellite-unstable (as opposed to stable) tumors and hypermethylation at miR-18b with sporadic disease (as opposed to Lynch syndrome).
|
21327300 |
2011 |
Lynch Syndrome
|
0.010 |
Biomarker
|
disease |
BEFREE |
In particular, hypermethylation at miR-148a and miR-152 was associated with microsatellite-unstable (as opposed to stable) tumors and hypermethylation at miR-18b with sporadic disease (as opposed to Lynch syndrome).
|
21327300 |
2011 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
COPZ2 displays no tumor-suppressive activities, but it harbors microRNA 152, which is silenced in tumor cells concurrently with COPZ2 and acts as a tumor suppressor in vitro and in vivo.
|
21746916 |
2011 |
Malignant Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Our findings define a central role for miR-152 in endometrial cancer, and they also suggest its use in new therapeutic strategies to treat this cancer.
|
21868754 |
2011 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Notably, restoration of miR-152 expression in endometrial cancer cell lines was sufficient to inhibit tumor cell growth in vitro and in vivo.
|
21868754 |
2011 |
Primary malignant neoplasm
|
0.080 |
Biomarker
|
group |
BEFREE |
Our findings define a central role for miR-152 in endometrial cancer, and they also suggest its use in new therapeutic strategies to treat this cancer.
|
21868754 |
2011 |
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 |
Malignant neoplasm of endometrium
|
0.040 |
Biomarker
|
disease |
BEFREE |
Our findings define a central role for miR-152 in endometrial cancer, and they also suggest its use in new therapeutic strategies to treat this cancer.
|
21868754 |
2011 |
Endometrial Carcinoma
|
0.040 |
Biomarker
|
disease |
BEFREE |
Our findings define a central role for miR-152 in endometrial cancer, and they also suggest its use in new therapeutic strategies to treat this cancer.
|
21868754 |
2011 |
Carcinogenesis
|
0.060 |
Biomarker
|
phenotype |
BEFREE |
Taken together, miR-152 and miR-148a may be involved in the carcinogenesis of ovarian cancer through deregulation of cell proliferation.
|
21971665 |
2012 |