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: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE Down-regulating Myoferlin inhibits the vasculogenic mimicry of melanoma via decreasing MMP-2 and inducing mesenchymal-to-epithelial transition. 29164766 2018
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE A novel matrix metalloproteinase-2 inhibitor triazolylmethyl aziridine reduces melanoma cell invasion, angiogenesis and targets ERK1/2 phosphorylation. 24246091 2014
CUI: C0025202
Disease: melanoma
melanoma
0.100 AlteredExpression disease BEFREE The myriad of biological effects exerted by elastokines on stromal and inflammatory cells led us to hypothesize that they might be main actors in elaborating a favorable cancerization field in melanoma; for instance these peptides could catalyze the vertical growth phase transition in melanoma through increased expression of gelatinase A and membrane-type 1 matrix metalloproteinase. 17498549 2007
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE When B16-BL6 melanoma cells or Lewis lung carcinoma cells were implanted intradermally, the tumor volumes at 3 weeks after implantation in the gelatinase A-deficient mice decreased by 39% for B16-BL6 melanoma and by 24% for Lewis lung carcinoma (P < 0.03 for each tumor).The number of lung colonies of i.v. injections fell by 54% for B16-BL6 melanoma and 77% for Lewis lung carcinoma (P < 0.014 and P < 0.0015, respectively). 9500469 1998
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE Stromal cells as the major source for matrix metalloproteinase-2 in cutaneous melanoma. 16047212 2005
CUI: C0025202
Disease: melanoma
melanoma
0.100 AlteredExpression disease BEFREE This novel mechanism of action of wild-type p53 gene transfer may contribute to its antitumor effect by downregulating cell invasion and matrix metalloproteinase-2 secreted levels in mutated p53 human melanoma cell lines. 10844565 2000
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE Plating cells onto type I or type IV collagen did not trigger pro-MMP-2 activation; on the contrary, conversion of pro-MMP-2 to its active form could be evidenced when melanoma cell lines were seeded in a three dimensional type I collagen lattice. 10763911 1999
CUI: C0025202
Disease: melanoma
melanoma
0.100 AlteredExpression disease BEFREE Activation of metalloproteinase (MMP) 2 expression greatly contributed to the BRG1 induced increase in melanoma invasiveness. 20969766 2010
CUI: C0025202
Disease: melanoma
melanoma
0.100 AlteredExpression disease BEFREE Therefore, CA can be characterized as a novel V-ATPase inhibitor for the treatment of melanoma that may inhibit invasion and metastasis by downregulating the expression of MMP-2 and -9. 29113270 2017
CUI: C0025202
Disease: melanoma
melanoma
0.100 AlteredExpression disease BEFREE Kinase activation led to increased MMP-2 and MT1-MMP expression and melanoma cell migration induced by hHK-1. 27458061 2016
CUI: C0025202
Disease: melanoma
melanoma
0.100 AlteredExpression disease BEFREE Additionally, alterations of SOCS-1 expression profoundly affected the expression of matrix metalloproteinase-2 (MMP-2), basic fibroblast growth factor (bFGF), and vascular endothelial growth factor (VEGF) and the melanoma cell invasion and angiogenesis. 19047140 2008
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE Since AP-2 also regulates other genes that are involved in the progression of human melanoma such as c-KIT, E-cadherin, MMP-2, and p21(WAF-1), we propose that loss of AP-2 is a crucial event in the development of malignant melanoma. 9632718 1998
CUI: C0025202
Disease: melanoma
melanoma
0.100 AlteredExpression disease BEFREE The findings indicate that NCTD inhibits tumor growth and VM formation of melanoma both <i>in vitro</i> and <i>in vivo</i> by suppressing matrix metalloproteinase-2 expression. 28454306 2017
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE We show that METTL3 is upregulated in human melanoma and plays a role in invasion/migration through MMP2. 30762711 2019
CUI: C0025202
Disease: melanoma
melanoma
0.100 GeneticVariation disease BEFREE Only 4 of the breast/colorectal 'hill' type CAN genes (SMAD4, MYO18B, NAV3 and MMP2) were also mutated in melanoma and pancreatic carcinoma, while none was altered in glioblastoma. 19058223 2009
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE Melanoma metastasis requires migration and invasion of the malignant tumour cells driven by proteolytic remodelling of the extracellular matrix (ECM) executed by matrix metalloproteinases (MMPs), particularly MMP-2 and MMP-9. 31020875 2019
CUI: C0025202
Disease: melanoma
melanoma
0.100 AlteredExpression disease BEFREE In parallel to CD44v3, MMP-2 expression (determined using immunohistochemistry) was significantly elevated (P<0.05) but only in the organ metastatic group of MM. 11764382 2001
CUI: C0025202
Disease: melanoma
melanoma
0.100 AlteredExpression disease LHGDN Hyaluronan fragments induce cytokine and metalloprotease upregulation in human melanoma cells in part by signalling via TLR4. 18031543 2008
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE We also demonstrate that: (1) among the major pro-angiogenic genes, FGF-2 was not increased before or after irradiation and vascular endothelial growth factor strongly inhibited after irradiation; (2) expression of two important metalloproteinases, matrix metalloproteinase 2 and 9, involved in melanoma metastasis were decreased before and after irradiation; (3) expression of their major inhibitor, tissue inhibitor of metalloproteinase, was mainly upregulated; and (4) that invasion of BRCA1 downregulated cells was modified. 15009718 2004
CUI: C0025202
Disease: melanoma
melanoma
0.100 AlteredExpression disease LHGDN 30%) attenuated the invasive activity of melanoma cells in a cell-based invasion assay and reduced MMP2 activity in the supernatant of melanoma cells. 17845054 2007
CUI: C0025202
Disease: melanoma
melanoma
0.100 AlteredExpression disease BEFREE We demonstrated that anterior lens capsule type IV collagen or specifically the synthetic peptide alpha3(IV) 185-203 inhibited both the migration of melanoma or fibrosarcoma cells as well as the activation of membrane-bound MMP-2 by decreasing the expressions of MT1-MMP and the beta3 integrin subunit. 10667602 2000
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE The caspase-3-mediated promotion of melanoma cell motility may be because of the cleavage of matrix metalloproteinase-2. 23695439 2013
CUI: C0025202
Disease: melanoma
melanoma
0.100 AlteredExpression disease BEFREE Previously, we have shown that the progression of human melanoma to the metastatic phenotype is associated with loss of AP-2 expression and deregulation of target genes such as MUC18/MCAM, c-KIT, and MMP-2. 12789289 2003
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease LHGDN Immunolabeling of melanoma cells with antibodies specific for MMP-2 and MMP-9 led to the identification of two distinct populations of small cytoplasmatic vesicles containing MMP-2 or MMP-9, respectively. 15604254 2004
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE Because MMP-2 activity is critical for melanoma progression, the MMP-2 peptide should be cross-presented by most progressing melanomas and represents a unique antigen for vaccine therapy of these tumors. 15998788 2005