Malignant neoplasm of lung
|
0.040 |
AlteredExpression
|
disease |
BEFREE |
In this study, we compared lung fibroblasts isolated from patients with idiopathic pulmonary fibrosis (F-IPF) and from patients undergoing resectional surgery for lung cancer (F-nl) with respect to their capacity for PGE2 synthesis and their expression and regulation of cyclooxygenase (COX) proteins.
|
7706493 |
1995 |
Carcinoma of lung
|
0.040 |
AlteredExpression
|
disease |
BEFREE |
In this study, we compared lung fibroblasts isolated from patients with idiopathic pulmonary fibrosis (F-IPF) and from patients undergoing resectional surgery for lung cancer (F-nl) with respect to their capacity for PGE2 synthesis and their expression and regulation of cyclooxygenase (COX) proteins.
|
7706493 |
1995 |
Primary malignant neoplasm of lung
|
0.040 |
AlteredExpression
|
disease |
BEFREE |
In this study, we compared lung fibroblasts isolated from patients with idiopathic pulmonary fibrosis (F-IPF) and from patients undergoing resectional surgery for lung cancer (F-nl) with respect to their capacity for PGE2 synthesis and their expression and regulation of cyclooxygenase (COX) proteins.
|
7706493 |
1995 |
Leigh Disease
|
0.050 |
Biomarker
|
disease |
BEFREE |
The results indicate a defective COX holoenzyme complex in patients with Leigh syndrome and suggest different molecular origins of the defect.
|
8781533 |
1996 |
Leigh Disease
|
0.050 |
Biomarker
|
disease |
BEFREE |
This result demonstrates that all our cases were genetically homogeneous, and suggests that a major nuclear disease locus is associated with several, perhaps most, of the cases of infantile COX(-) Leigh's syndrome.
|
9063742 |
1997 |
Mitochondrial Diseases
|
0.040 |
GeneticVariation
|
group |
BEFREE |
A generalized defect of complex IV (cytochrome C oxidase, COX) is frequently found in subacute necrotizing encephalomyelopathy (Leigh's syndrome), the most common mitochondrial disorder in infancy.
|
9063742 |
1997 |
Cytochrome-c Oxidase Deficiency
|
0.350 |
GeneticVariation
|
disease |
BEFREE |
No mitochondrial cytochrome oxidase (COX) gene mutations in 18 cases of COX deficiency.
|
9402980 |
1997 |
Harderoporphyria
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
In the present study, molecular investigations in a second family with neonatal hemolytic anemia and harderoporphyria revealed two heterozygous point mutations in the COX gene.
|
9454777 |
1998 |
Alzheimer's Disease
|
0.060 |
Biomarker
|
disease |
BEFREE |
We propose the novel hypothesis that the COX defect and resulting oxidative stress in AD may pathologically activate the MTP, resulting in lower delta psi m and the release of mitochondrial factors involved in apoptosis.
|
9675105 |
1998 |
Carcinoma
|
0.020 |
Biomarker
|
group |
BEFREE |
Two Cox genes have been cloned (Cox-1 and Cox-2), of which Cox-2 has recently been found to be expressed in several human carcinomas.
|
9823297 |
1998 |
Mitochondrial Diseases
|
0.040 |
GeneticVariation
|
group |
BEFREE |
Sequence analysis of SURF-1 revealed mutations in numerous DNA samples from LD(COX-) patients, indicating that this gene is responsible for the major complementation group in this important mitochondrial disorder.
|
9837813 |
1998 |
Rheumatoid Arthritis
|
0.010 |
Biomarker
|
disease |
BEFREE |
Prostaglandins (PG) formed by cyclooxygenase (COX) enzymes are important mediators of inflammation in rheumatoid arthritis.
|
10701683 |
2000 |
Colon Carcinoma
|
0.030 |
AlteredExpression
|
disease |
BEFREE |
Nonsteroidal antiinflammatory drugs inhibiting cyclooxygenase (COX) enzyme activity in both its constitutive (COX-1) and inducible (COX-2) isoforms were shown also to inhibit the development of colon carcinoma in animal models.
|
10931458 |
2000 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
Mice fed various COX blocking agents also showed a decline in tumor size.
|
11313976 |
2001 |
Malignant tumor of cervix
|
0.010 |
Biomarker
|
disease |
BEFREE |
Cervical cancer is thus considered an important clinical problem in sub-Saharan AFRICA: Recent studies have suggested that epithelial tumors may be regulated by cyclooxygenase (COX) enzyme products.
|
11344234 |
2001 |
Cervix carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Cervical cancer is thus considered an important clinical problem in sub-Saharan AFRICA: Recent studies have suggested that epithelial tumors may be regulated by cyclooxygenase (COX) enzyme products.
|
11344234 |
2001 |
Epithelioma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Cervical cancer is thus considered an important clinical problem in sub-Saharan AFRICA: Recent studies have suggested that epithelial tumors may be regulated by cyclooxygenase (COX) enzyme products.
|
11344234 |
2001 |
cervical cancer
|
0.010 |
Biomarker
|
disease |
BEFREE |
Cervical cancer is thus considered an important clinical problem in sub-Saharan AFRICA: Recent studies have suggested that epithelial tumors may be regulated by cyclooxygenase (COX) enzyme products.
|
11344234 |
2001 |
Carcinogenesis
|
0.100 |
AlteredExpression
|
phenotype |
BEFREE |
Cyclooxygenase-2 (COX-2) is an inducible form of COX and is overexpressed in diverse tumors, raising the possibility of a role for COX-2 in carcinogenesis.
|
11381123 |
2001 |
Tumor Cell Invasion
|
0.060 |
Biomarker
|
phenotype |
BEFREE |
In contrast, invasion was induced by the TXA2-R mimetic U-46619, constitutively activated forms of the heterotrimeric G-proteins Galphaq (AGalphaq), Galpha12, Galpha13 (AGalpha12/13), which are signaling elements downstream of TXA2-R. Ectopic overexpression of pS2 cDNA and protein in MDCKts.src-pS2 cells and human colorectal cancer cells HCT8/S11-pS2 initiate distinct invasion signals that are Rho independent and COX and TXA2-R dependent.
|
11427483 |
2001 |
Malignant Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Two Cox genes have been cloned, and expression of Cox-2 mRNA and protein has been shown to be elevated in several human malignancies and in animal models of carcinogenesis.
|
11448905 |
2001 |
Carcinogenesis
|
0.100 |
AlteredExpression
|
phenotype |
BEFREE |
Two Cox genes have been cloned, and expression of Cox-2 mRNA and protein has been shown to be elevated in several human malignancies and in animal models of carcinogenesis.
|
11448905 |
2001 |
Neoplasm Metastasis
|
0.080 |
Biomarker
|
phenotype |
BEFREE |
Taken together, these results indicate that non-steroidal anti-inflammatory drugs suppress MMP-2 expression via repression of transcription and support the notion that COX inhibitors may be useful in inhibition and/or prevention of metastasis.
|
11728453 |
2001 |
Carcinogenesis
|
0.100 |
Biomarker
|
phenotype |
BEFREE |
The aim of this article is to present a review of COX genes, the prostaglandin-cyclooxygenase relationship, the role of COX-2 in carcinogenesis and the rationale for targeting COX-2 with NSAIDs for cancer chemoprevention.
|
12494894 |
2003 |
Neoplasms
|
0.100 |
Biomarker
|
group |
BEFREE |
These results suggest an involvement of COX-2 in the control of tumor-dependent angiogenesis and growth in certain pancreatic cancers and provide the rational for inhibition of the COX pathway as an effective therapeutic approach for pancreatic tumors.
|
12533667 |
2003 |