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 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 Furthermore, Pin1 inhibition also resulted in decreased phosphorylation of Akt and repressed expression of C-Jun N-terminal kinase and pro-matrix metalloproteinase 2, which were associated closely with the development of melanoma. 23067222 2013
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE To better understand the potential impact of these mutant amino acids on protease function and cancer progression, we established a bioinformatics approach to assessing the impact of melanoma mutants, among a previously defined set of extracellular matrix (ECM) structural proteins, on the sensitivity of matrix metalloproteinase-2 (MMP2), extensively associated with melanoma. 31019293 2019
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE For instance, a RAR alpha antagonist suppressed MMP-1 and MMP-2 synthesis in the melanoma cell line, but not in the FaDu or SCC-25 cells. 10415749 1999
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE Together, these data indicate that activation of Jak/Vav/Rho GTPase pathway by CXCL12 is a key signaling event for MT1-MMP/MMP-2-dependent melanoma cell invasion. 16397238 2006
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE More than 90% tumors expressed alpha6a, beta1, beta3 and beta6 (non-melanoma), and alpha5a, alpha6a and MMP2 (MM). 18251742 2008
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE We used a bioinformatics approach to assess the impact of amino acid (AA) substitutions on the sensitivity of CECMPs to proteases relevant to melanoma and on the binding affinities for HLA class I. CECMP peptides with AA substitutions overwhelmingly reflect increased sensitivity to proteases implicated in melanoma development (MME, CTSS, MMP2, CTSD, CTSL) in comparison to the wild-type peptide sequences. 29047110 2018
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE In this study, the prognostic value of MMP-2 and Ki-67 via immuno-staining in head and neck melanoma is investigated. 25313763 2015
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease LHGDN Interestingly, male patients with a melanoma with overexpression of MMP-2 showed a 10-year disease-specific survival of only 41% compared with 77% in other male patients (P = .003). 18187184 2008
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE Also, M21/OPN cells exhibit increased motility, which is markedly reduced upon treatment with inhibitors to alpha(v) and MMP-2. 16631740 2006
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease LHGDN 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
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE Importantly, knocking down CD147 attenuates MMP2 response to hypoxia in melanoma cell lines. 24090196 2014
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease LHGDN Our pilot study demonstrates that MMP2, MMP14, MMP9, and MaxND might be used as prognostic markers in patients with sinonasal and oral malignant melanoma. 18045645 2008
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease LHGDN Upregulation of MMP-2 activation by ED led to enhanced melanoma cells invasion through S-Gal occupancy. 15009703 2004
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 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 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 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 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 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 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 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 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