Myocardial Ischemia
|
0.300 |
Biomarker
|
disease |
CTD_human |
Cardioplegia prevents ischemia-induced transcriptional alterations of cytoprotective genes in rat hearts: a DNA microarray study.
|
16214533 |
2005 |
Cardiomegaly
|
0.200 |
Biomarker
|
phenotype |
RGD |
The profile of cardiac cytochrome c oxidase (COX) expression in an accelerated cardiac-hypertrophy model.
|
16132109 |
2005 |
Hypertensive disease
|
0.200 |
Biomarker
|
group |
RGD |
The profile of cardiac cytochrome c oxidase (COX) expression in an accelerated cardiac-hypertrophy model.
|
16132109 |
2005 |
Neoplasms
|
0.020 |
AlteredExpression
|
group |
BEFREE |
Furthermore, statistical analysis showed the COX5B expression level was significantly associated with clinical stage and lymph node status, while there were no correlations between COX5B expression and age or tumor size.
|
29180880 |
2017 |
Neoplasms
|
0.020 |
Biomarker
|
group |
BEFREE |
An immunohistochemical analysis of oropharyngeal carcinomas showed an enhanced antitumoral immune response (CD8/CD4 ratio) together with increased levels of proteins involved in transmembranous metabolite transportation (GLUT1 and CD147) and respiratory metabolism (COX5B) in HPV-positive tumors as compared to HPV-negative tumors. mRNA and Western blot analyses of an HPV-positive and HPV-negative HNSCC cell line revealed metabolic characteristics similar to the in vivo situation.
|
25027580 |
2014 |
Conventional (Clear Cell) Renal Cell Carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Systematic expression analysis of the mitochondrial respiratory chain protein subunits identifies COX5B as a prognostic marker in clear cell renal cell carcinoma.
|
31280487 |
2019 |
Malignant Neoplasms
|
0.010 |
Biomarker
|
group |
BEFREE |
The Cancer Genome Atlas analysis confirmed that patients with a favorable immune and metabolic gene signature (high CD8A, high COX5B, low GLUT1) had improved short- and long-term survival.
|
29107073 |
2018 |
Squamous cell carcinoma of the head and neck
|
0.010 |
Biomarker
|
disease |
BEFREE |
In the chemoradiotherapy-treated HNSCC cohort, mitochondrial-rich (COX5B) metabolism correlated with increased and glucose-dependent (GLUT1) metabolism with decreased intratumoral CD8/CD4 ratios.
|
29107073 |
2018 |
Primary malignant neoplasm
|
0.010 |
Biomarker
|
group |
BEFREE |
The Cancer Genome Atlas analysis confirmed that patients with a favorable immune and metabolic gene signature (high CD8A, high COX5B, low GLUT1) had improved short- and long-term survival.
|
29107073 |
2018 |
Malignant neoplasm of breast
|
0.010 |
Biomarker
|
disease |
BEFREE |
Cumulatively, our findings suggest that COX5B might serve as an important prognostic factor for breast cancer.
|
28592145 |
2017 |
Glioblastoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
We found that COX5B was significantly upregulated in 67 of 87 (77.0%) glioma and glioblastoma tissues, compared with adjacent tissue (<i>p</i><0.01).
|
29180880 |
2017 |
Glioma
|
0.010 |
Biomarker
|
disease |
BEFREE |
These data indicate that COX5B may be implicated in glioma pathogenesis and as a biomarker for identification of the pathological grade of glioma.
|
29180880 |
2017 |
Neoplasm Metastasis
|
0.010 |
Biomarker
|
phenotype |
BEFREE |
In this context, we developed a new Myc-based Mito-Signature consisting of 3 mitochondrial genes (HSPD1; COX5B; TIMM44) for effectively predicting tumor recurrence (HR=4.69; p=2.4e-08) and distant metastasis (HR=4.94; p=2.8e-07), in ER(+) in breast cancer patients.
|
29080556 |
2017 |
Septicemia
|
0.010 |
Biomarker
|
disease |
BEFREE |
For future research, COX5B should be evaluated as a biomarker in both human urine and serum to identify sepsis.
|
28246552 |
2017 |
Sepsis
|
0.010 |
Biomarker
|
disease |
BEFREE |
For future research, COX5B should be evaluated as a biomarker in both human urine and serum to identify sepsis.
|
28246552 |
2017 |
Adult Glioblastoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
We found that COX5B was significantly upregulated in 67 of 87 (77.0%) glioma and glioblastoma tissues, compared with adjacent tissue (<i>p</i><0.01).
|
29180880 |
2017 |
Childhood Glioblastoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
We found that COX5B was significantly upregulated in 67 of 87 (77.0%) glioma and glioblastoma tissues, compared with adjacent tissue (<i>p</i><0.01).
|
29180880 |
2017 |
Recurrent tumor
|
0.010 |
GeneticVariation
|
phenotype |
BEFREE |
In this context, we developed a new Myc-based Mito-Signature consisting of 3 mitochondrial genes (HSPD1; COX5B; TIMM44) for effectively predicting tumor recurrence (HR=4.69; p=2.4e-08) and distant metastasis (HR=4.94; p=2.8e-07), in ER(+) in breast cancer patients.
|
29080556 |
2017 |
Breast Carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Cumulatively, our findings suggest that COX5B might serve as an important prognostic factor for breast cancer.
|
28592145 |
2017 |
Invasive Ductal Breast Carcinoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
We carried out immunohistochemistry on tissue microarrays of 244 patients with invasive ductal breast carcinoma to detected COX5B expression.
|
28592145 |
2017 |
Glioblastoma Multiforme
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
We found that COX5B was significantly upregulated in 67 of 87 (77.0%) glioma and glioblastoma tissues, compared with adjacent tissue (<i>p</i><0.01).
|
29180880 |
2017 |
ovarian neoplasm
|
0.010 |
Biomarker
|
disease |
BEFREE |
We have obtained three key genes (C9orf16, COX5B and ACTB) for ovarian cancer on the basis of mAP-KL method and MIN analysis.
|
27383302 |
2016 |
Malignant neoplasm of ovary
|
0.010 |
Biomarker
|
disease |
BEFREE |
We have obtained three key genes (C9orf16, COX5B and ACTB) for ovarian cancer on the basis of mAP-KL method and MIN analysis.
|
27383302 |
2016 |
Carcinoma, Ovarian Epithelial
|
0.010 |
Biomarker
|
disease |
BEFREE |
We have obtained three key genes (C9orf16, COX5B and ACTB) for ovarian cancer on the basis of mAP-KL method and MIN analysis.
|
27383302 |
2016 |
Oropharyngeal disorders
|
0.010 |
AlteredExpression
|
group |
BEFREE |
An immunohistochemical analysis of oropharyngeal carcinomas showed an enhanced antitumoral immune response (CD8/CD4 ratio) together with increased levels of proteins involved in transmembranous metabolite transportation (GLUT1 and CD147) and respiratory metabolism (COX5B) in HPV-positive tumors as compared to HPV-negative tumors. mRNA and Western blot analyses of an HPV-positive and HPV-negative HNSCC cell line revealed metabolic characteristics similar to the in vivo situation.
|
25027580 |
2014 |