Tumor Cell Invasion
|
0.020 |
Biomarker
|
phenotype |
BEFREE |
Furthermore, overexpression of SphK1 increased S1P levels, and the exogenous addition of S1P increased liver cell migration and invasion through the EDG1 receptor.
|
22098666 |
2012 |
Secondary malignant neoplasm of liver
|
0.010 |
Biomarker
|
disease |
BEFREE |
The results from this study provide strong evidence of a role for the SphK1/S1P/EDG1 pathway in liver metastasis, thus making it an attractive therapeutic target for the development of new anti-HCC drugs.
|
22098666 |
2012 |
Liver carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Sphingosine kinase 1 promotes tumour cell migration and invasion via the S1P/EDG1 axis in hepatocellular carcinoma.
|
22098666 |
2012 |
Myopathy
|
0.010 |
AlteredExpression
|
group |
BEFREE |
We find that the muscle degeneration observed in a C. elegans model of dystrophin-based muscular dystrophy can be suppressed by clp-1 inactivation and that nemadipine-A inhibition of the EGL-19 calcium channel reveals that Ca(2+) dysfunction underlies the C. elegans MyoD model of myopathy.
|
22479198 |
2012 |
Muscle degeneration
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
These studies show that the atypical calpain gene, clp-1, contributes to muscle degeneration and reveal that clp-1 activity is sensitive to genetic manipulation of [Ca(2+)](i).
|
22479198 |
2012 |
Left Ventricular Hypertrophy
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
Hexamethylene bis-acetamide inducible protein 1 (HEXIM1) is a negative regulator of positive transcription elongation factor b (P-TEFb), which activates RNA polymerase II (RNAPII)-dependent transcription and whose activation is strongly associated with left ventricular hypertrophy.
|
23300697 |
2012 |
Right Ventricular Hypertrophy
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
Taken together, these findings indicate that cardiomyocyte-specific overexpression of HEXIM1 inhibits progression to RVH under chronic hypoxia, most possibly via inhibition of P-TEFb-mediated enlargement of cardiomyocytes.
|
23300697 |
2012 |
Hypertensive disease
|
0.010 |
AlteredExpression
|
group |
BEFREE |
Cardiomyocyte-specific overexpression of HEXIM1 prevents right ventricular hypertrophy in hypoxia-induced pulmonary hypertension in mice.
|
23300697 |
2012 |
Idiopathic pulmonary arterial hypertension
|
0.010 |
Biomarker
|
disease |
BEFREE |
Moreover, we created cardiomyocyte-specific HEXIM1 transgenic mice and revealed that HEXIM1 ameliorates RVH and prevents RV dilatation in hypoxia-induced PAH model.
|
23300697 |
2012 |
Tumor Cell Invasion
|
0.020 |
AlteredExpression
|
phenotype |
BEFREE |
The consequence of HEXIM1 down-regulation of HIF-1α protein expression is attenuated expression of HIF-1α target genes in addition to VEGF and inhibition of HIF-1α-regulated cell invasion.
|
24015760 |
2013 |
Right Ventricular Hypertrophy
|
0.020 |
Biomarker
|
disease |
BEFREE |
Thus, we conclude that HEXIM1 could prevent RV hypertrophy, at least in part, via suppression of myocardial angiogenesis through down-regulation of HIF-1α and VEGF in the myocardium under hypoxic condition.
|
25301555 |
2014 |
Liver Cirrhosis, Experimental
|
0.300 |
Biomarker
|
disease |
CTD_human |
Systems level analysis and identification of pathways and networks associated with liver fibrosis.
|
25380136 |
2014 |
Malignant neoplasm of breast
|
0.020 |
Biomarker
|
disease |
BEFREE |
Use of a novel cytotoxic HEXIM1 peptide in the directed breast cancer therapy.
|
26734838 |
2016 |
Breast Carcinoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
Use of a novel cytotoxic HEXIM1 peptide in the directed breast cancer therapy.
|
26734838 |
2016 |
Neoplasms
|
0.090 |
AlteredExpression
|
group |
BEFREE |
In melanoma, we identify HEXIM1, a transcription elongation regulator, as a melanoma tumor suppressor that responds to nucleotide stress.HEXIM1 expression is low in melanoma.
|
27058786 |
2016 |
Malignant Neoplasms
|
0.060 |
Biomarker
|
group |
BEFREE |
HEXIM1 plays an important role in inhibiting cancer cell-specific gene transcription while also facilitating anti-cancer gene expression.
|
27058786 |
2016 |
Primary malignant neoplasm
|
0.060 |
Biomarker
|
group |
BEFREE |
HEXIM1 plays an important role in inhibiting cancer cell-specific gene transcription while also facilitating anti-cancer gene expression.
|
27058786 |
2016 |
melanoma
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
Our study reveals an important role for HEXIM1 in coupling nucleotide metabolism with transcriptional regulation in melanoma.
|
27058786 |
2016 |
Neoplasms
|
0.090 |
Biomarker
|
group |
BEFREE |
Nucleotide stress induces the tumor suppressor HEXIM1 to suppress melanoma.
|
27102073 |
2016 |
melanoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
Nucleotide stress induces the tumor suppressor HEXIM1 to suppress melanoma.
|
27102073 |
2016 |
Neoplasms
|
0.090 |
AlteredExpression
|
group |
BEFREE |
We have been studying the role of Hexamethylene bisacetamide (HMBA) Induced Protein 1 (HEXIM1) as a tumor suppressor whose expression is decreased in tamoxifen resistant and metastatic breast cancer.
|
27238569 |
2016 |
Neoplasm Metastasis
|
0.020 |
Biomarker
|
phenotype |
BEFREE |
Clinically relevant HEXIM1 activities that are also induced by 4a1 include enhancement of the inhibitory effects of tamoxifen and inhibition of breast tumor metastasis.
|
27238569 |
2016 |
Mammary Neoplasms
|
0.020 |
Biomarker
|
group |
BEFREE |
Clinically relevant HEXIM1 activities that are also induced by 4a1 include enhancement of the inhibitory effects of tamoxifen and inhibition of breast tumor metastasis.
|
27238569 |
2016 |
Carcinoma breast stage IV
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
We have been studying the role of Hexamethylene bisacetamide (HMBA) Induced Protein 1 (HEXIM1) as a tumor suppressor whose expression is decreased in tamoxifen resistant and metastatic breast cancer.
|
27238569 |
2016 |
Neoplasms
|
0.090 |
Biomarker
|
group |
BEFREE |
HEXIM1 as a Robust Pharmacodynamic Marker for Monitoring Target Engagement of BET Family Bromodomain Inhibitors in Tumors and Surrogate Tissues.
|
27903752 |
2017 |