MMP2, matrix metallopeptidase 2, 4313

N. diseases: 1021; N. variants: 43
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.300 Biomarker disease BEFREE This was associated with a vascular site-specific effect of Ikkα<sup>AA/AA</sup> knock-in on atherosclerosis: in the aortic root, Ikkα<sup>AA/AA</sup> knock-in decreased lesion size by 22.0 ± 7.7% (p < 0.01), reduced absolute lesional smooth muscle cell numbers and lowered pro-atherogenic MMP2. 31733453 2020
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.300 Biomarker disease BEFREE <i>Background</i>: The expression of matrix metalloproteinases 2/9 (MMP-2/9) has been implicated in arterial remodeling and inflammation in atherosclerosis. 30513758 2018
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.300 Biomarker disease BEFREE Here, we report that bone morphogenetic protein 2 (BMP-2) leads to enrichment of CD44 and F-actin stress fiber and secretion of matrix metalloproteinases-2 (MMP-2) during hypoxia in vitro and following artificial hypoxia-induced atherosclerosis exacerbation in vivo. 29750899 2018
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.300 AlteredExpression disease BEFREE Additionally, ginkgetin reduced the mRNA and protein expression of MMP-2 and MMP-9 in thoracic aortas of rats with atherosclerosis. 29579712 2018
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.300 AlteredExpression disease BEFREE <b>Conclusion:</b> RDN promoted atherosclerosis in apolipoprotein E-deficient mice infused with angiotensin II associated with upregulation of MMP-2. 28450836 2017
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.300 Biomarker disease BEFREE Our data have showed a large increase in the enzyme MMP-2 and 9 in the urine of CAS and A patients in comparison with healthy controls and indicated this method as an easy marker for the monitoring of the development of atherosclerosis. 28500763 2017
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.300 AlteredExpression disease BEFREE These findings suggest that FXa/FIIa inhibition limits aortic aneurysm and atherosclerosis severity due to down-regulation of vascular PAR-2-mediated Smad2/3 signalling and MMP2 expression. 28220880 2017
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.300 Biomarker disease BEFREE Systematic (circulated in plasma) neutrophil gelatinase come from multiple sources; it may be synthesized in the liver, secreted from activated neutrophils or macrophages, or derive from atherosclerosis or inflammatory endothelial cells [17]. 27708207 2016
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.300 AlteredExpression disease BEFREE Cholestin reduces TNF-α-stimulated MMP-2 and MMP-9 expression as well as downregulating NF-κB activation and intracellular ROS formation in HASMCs, supporting the notion that the natural compound Cholestin may have potential application in clinical atherosclerosis disease. 22060290 2011
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.300 GeneticVariation disease BEFREE MMP2 genetic variation is associated with measures of fibrous cap thickness: The Atherosclerosis Risk in Communities Carotid MRI Study. 20064641 2010
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.300 Biomarker disease LHGDN Serum matrix metalloproteinase-2 and increased oxidative stress are associated with carotid atherosclerosis in hemodialyzed patients. 16510149 2007
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.300 Biomarker disease RGD Our results suggest that the expression of CD40 and CD40L in the blood cells and the activities of MMP-2 and MMP-9 in plasma were higher in As group than those in Normal group, indicating that they may contribute to the formation of atherosclerosis. 16317521 2006
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis
0.300 Biomarker disease BEFREE However, since these cell lines did not show a fully malignant phenotype, we concluded that, in addition to the degradation of extracellular matrix macromolecules, including basement membrane components by MMP-2, -3, and/or -9, some additional factors must be involved for the malignancy of fully transformed cells and that these immortalized human aortic SMC, which share many characteristics with normal SMC, will prove useful to study the role(s) of metalloproteinases in atherosclerosis. 1333771 1992