Body Height
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
|
30595370 |
2019 |
Reticulocyte count (procedure)
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
|
27863252 |
2016 |
Neoplasms
|
0.050 |
Biomarker
|
group |
BEFREE |
USP10 regulates Musashi-2 stability via deubiquitination and promotes tumour proliferation in colon cancer.
|
30604502 |
2019 |
Neoplasms
|
0.050 |
Biomarker
|
group |
BEFREE |
However, the clinicopathological features and survival analysis indicated that the USP10 and MSH2 proteins were not associated with clinical features, including age, sex, tumor size, Tumor-Node-Metastasis stage and tumor cell differentiation, along with the prognosis of NSCLC.
|
30655874 |
2019 |
Neoplasms
|
0.050 |
Biomarker
|
group |
BEFREE |
Knockdown of USP10 promotes tumor growth and invasion both in vitro and in vivo.
|
28852924 |
2018 |
Neoplasms
|
0.050 |
Biomarker
|
group |
BEFREE |
Collectively, our results uncover an undescribed mechanism where USP10, as a tumor suppressor, negatively regulates mTORC1 activation and AKT phosphorylation by stabilizing AMPKα and PTEN in HCC cells.
|
30056112 |
2018 |
Neoplasms
|
0.050 |
Biomarker
|
group |
BEFREE |
Our study discovered crosstalk between two tumor-suppressive genes in regulating cell-cycle progression and proliferation and showed that dysregulated USP10 function promotes tumorigenesis through SIRT6 degradation.
|
24332849 |
2013 |
Carcinogenesis
|
0.040 |
Biomarker
|
phenotype |
BEFREE |
Forced expression of USP10 remarkably increases KLF4 protein level by blocking the latter degradation, whereas the depletion of USP10 promotes KLF4 degradation and thus enhances tumorigenesis.
|
31748695 |
2019 |
Carcinogenesis
|
0.040 |
AlteredExpression
|
phenotype |
BEFREE |
Collectively, these results suggest that downregulation of USP10 protein serves an important function in the tumorigenesis of NSCLC, and the level of USP10 protein is positively correlated with that of MSH2 protein in NSCLC tissues, which may indicate that USP10 also stabilizes the MSH2 protein in patients with lung cancer.
|
30655874 |
2019 |
Carcinogenesis
|
0.040 |
Biomarker
|
phenotype |
BEFREE |
Collectively, these data suggest that miR-191 could promote pancreatic cancer progression through targeting USP10, implicating a novel mechanism for the tumorigenesis.
|
25168367 |
2014 |
Carcinogenesis
|
0.040 |
Biomarker
|
phenotype |
BEFREE |
Our study discovered crosstalk between two tumor-suppressive genes in regulating cell-cycle progression and proliferation and showed that dysregulated USP10 function promotes tumorigenesis through SIRT6 degradation.
|
24332849 |
2013 |
Malignant Neoplasms
|
0.030 |
PosttranslationalModification
|
group |
BEFREE |
A high degree of methylation in USP10 and p14ARF CpG islands was found by methylation specific PCR analysis in cancer than in normal tissues and cells.
|
31659108 |
2020 |
Primary malignant neoplasm
|
0.030 |
PosttranslationalModification
|
group |
BEFREE |
A high degree of methylation in USP10 and p14ARF CpG islands was found by methylation specific PCR analysis in cancer than in normal tissues and cells.
|
31659108 |
2020 |
Malignant Neoplasms
|
0.030 |
AlteredExpression
|
group |
BEFREE |
Therefore, USP10 protein expression was detected in 148 human non-small cell lung cancer (NSCLC) and 139 non-cancerous lung tissues using immunohistochemistry, whereas mRNA was investigated by Gene Expression Omnibus dataset and The Cancer Genome Atlas database analyses.
|
30655874 |
2019 |
Malignant neoplasm of lung
|
0.030 |
Biomarker
|
disease |
BEFREE |
Taken together, our results demonstrate that USP10 is a critical regulator of KLF4, pinpointing USP10-KLF4-TIMP3 axis as a promising therapeutic target in lung cancer.
|
31748695 |
2019 |
Malignant neoplasm of lung
|
0.030 |
Biomarker
|
disease |
BEFREE |
Additionally, whether the level of MSH2 protein is positively correlated with that of the USP10 protein in lung cancer tissues also remains unresolved.
|
30655874 |
2019 |
Carcinoma of lung
|
0.030 |
Biomarker
|
disease |
BEFREE |
Additionally, whether the level of MSH2 protein is positively correlated with that of the USP10 protein in lung cancer tissues also remains unresolved.
|
30655874 |
2019 |
Carcinoma of lung
|
0.030 |
Biomarker
|
disease |
BEFREE |
Taken together, our results demonstrate that USP10 is a critical regulator of KLF4, pinpointing USP10-KLF4-TIMP3 axis as a promising therapeutic target in lung cancer.
|
31748695 |
2019 |
Primary malignant neoplasm
|
0.030 |
AlteredExpression
|
group |
BEFREE |
Therefore, USP10 protein expression was detected in 148 human non-small cell lung cancer (NSCLC) and 139 non-cancerous lung tissues using immunohistochemistry, whereas mRNA was investigated by Gene Expression Omnibus dataset and The Cancer Genome Atlas database analyses.
|
30655874 |
2019 |
Primary malignant neoplasm of lung
|
0.030 |
Biomarker
|
disease |
BEFREE |
Taken together, our results demonstrate that USP10 is a critical regulator of KLF4, pinpointing USP10-KLF4-TIMP3 axis as a promising therapeutic target in lung cancer.
|
31748695 |
2019 |
Primary malignant neoplasm of lung
|
0.030 |
Biomarker
|
disease |
BEFREE |
Additionally, whether the level of MSH2 protein is positively correlated with that of the USP10 protein in lung cancer tissues also remains unresolved.
|
30655874 |
2019 |
Malignant Neoplasms
|
0.030 |
AlteredExpression
|
group |
BEFREE |
Importantly, USP10 is concomitantly highly expressed with Slug in cancer biopsies.
|
29803676 |
2018 |
Malignant neoplasm of lung
|
0.030 |
AlteredExpression
|
disease |
BEFREE |
USP10 was down-regulated in lung cancer.
|
28852924 |
2018 |
Carcinoma of lung
|
0.030 |
AlteredExpression
|
disease |
BEFREE |
USP10 was down-regulated in lung cancer.
|
28852924 |
2018 |
Primary malignant neoplasm
|
0.030 |
AlteredExpression
|
group |
BEFREE |
Importantly, USP10 is concomitantly highly expressed with Slug in cancer biopsies.
|
29803676 |
2018 |