HGF, hepatocyte growth factor, 3082

N. diseases: 671; N. variants: 22
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 HGF might be a factor in the innate and acquired resistance of melanoma to oncoprotein-targeted drugs. 30513872 2018
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE We summarize recent studies, which involved inhibition of the HGF/c-Met signaling in order to decrease melanoma growth and metastatic capacity. 29455657 2018
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE In this study we observed a dominant role for the HGF/MET axis in mediating resistance to BRAF and MEK inhibitors in models of BRAFV600E and NRAS mutant melanoma. 28147313 2017
CUI: C0025202
Disease: melanoma
melanoma
0.100 GeneticVariation disease BEFREE To address this question in vivo in a spontaneous melanoma model, we deleted ADAM-9 in mice carrying the hepatocyte growth factor (Hgf) transgene and knock-in mutation Cdk4<sup>R24C/R24C</sup>, demonstrated to spontaneously develop melanoma. 28553955 2017
CUI: C0025202
Disease: melanoma
melanoma
0.100 AlteredExpression disease BEFREE Higher serum/plasma HGF levels are associated with therapy resistance and/or metastasis, while lower HGF levels are associated with progression-free survival and overall survival after treatment with targeted drugs in lung cancer, gastric cancer, colon cancer, and malignant melanoma. 28064454 2017
CUI: C0025202
Disease: melanoma
melanoma
0.100 AlteredExpression disease BEFREE To determine whether hrIL-7/HGFβ has antitumor activity, we injected this hybrid cytokine into melanoma and colon cancer animal models, and then assessed the local tumor growth and tumor metastasis. 28861327 2017
CUI: C0025202
Disease: melanoma
melanoma
0.100 AlteredExpression disease BEFREE In this review, we summarize how the HGF/SF transgenic mouse has been used to reveal metastasis-regulating activity of four different genes (<i>CDK4</i><sup>R24C</sup>, <i>survivin</i> and <i>NME1/NME2</i>) in the context of UV-induced melanoma. 28788083 2017
CUI: C0025202
Disease: melanoma
melanoma
0.100 AlteredExpression disease BEFREE We further confirmed that the upregulation of HGF/MET signaling was evident in drug-resistant melanoma patient tissues and mouse xenografts. 27458138 2016
CUI: C0025202
Disease: melanoma
melanoma
0.100 AlteredExpression disease BEFREE The aim of this study was to analyze the pharmacokinetics of vemurafenib by a population approach and to evaluate the relationship between plasma drug exposure and pre-treatment plasma hepatocyte growth factor (HGF) levels with clinical effects (progression-free survival (PFS), peripheral lymphocytes depletion) in patients with metastatic BRAF<sup>V600</sup> mutated melanoma treated with single agent vemurafenib. 27378568 2016
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE The HGF-cMET signaling pathway in conferring stromal-induced BRAF-inhibitor resistance in melanoma. 26317169 2015
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE These results suggest that SPINT2 is associated with tumor-suppressive functions in melanoma by inhibiting an extracellular signal regulator of HGF, which is typically activated by tumor-stromal interactions. 25910030 2015
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE Consequent patient evaluation in collaboration with the Melanoma Institute Australia of a cohort of 41 melanoma specimens with extensive clinical annotation failed to validate HGF immunohistochemistry as a predictor of response to BRAF inhibitors. 24434899 2014
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE However, long-term curative effect was achieved by the augmentation of the CD-MSC/5FC regimen along with the inhibition of c-Met/hepatocyte growth factor signaling axis in this aggressive melanoma derivative. 25056607 2014
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE Although stimulation of melanoma N1 cells (GD3+ and GD3-) with either HGF or adhesion to CL-I did not show marked differences in the phosphorylation levels of Akt at Ser473 and Thr308 between two types of cells, simultaneous treatment resulted in definite and markedly increased activation of Akt in GD3+ cells. 24372645 2014
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE Interestingly, no differences were observed in the invasive characteristics of primary melanomas of HGF(+) and HGF(+) × [m1m2](+/-) strains, with both exhibiting invasion into the dermis and subcutis, indicating factors other than simple invasive activity were responsible for metastasis of HGF(+) × [m1m2](+/-) melanomas. 22699362 2013
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE In vivo, we used the HGF transgenic mouse model of UV-induced melanoma to demonstrate that topical treatment with l-selenomethionine results in a significant delay in the time required for UV-induced melanoma development, but also increases the rate of growth of those tumors once they appear. 23470450 2013
CUI: C0025202
Disease: melanoma
melanoma
0.100 GeneticVariation disease BEFREE Therefore, blockade of HGF-MET signalling might be a valid therapeutic strategy, in combination with BRAF inhibition, in BRAF(V600E/K) melanoma. 23802768 2013
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE Dual inhibition of RAF and either HGF or MET resulted in reversal of drug resistance, suggesting RAF plus HGF or MET inhibitory combination therapy as a potential therapeutic strategy for BRAF-mutant melanoma. 22763439 2012
CUI: C0025202
Disease: melanoma
melanoma
0.100 AlteredExpression disease BEFREE We show, by quantitative real time PCR, that all melanoma cell lines expressed genes for the RTK ligands such as HGF, IGF-1, and MSP. 21654344 2011
CUI: C0025202
Disease: melanoma
melanoma
0.100 AlteredExpression disease BEFREE Suppression of endogenous RasGRP3 expression in these melanoma cell lines reduced Ras-GTP formation as well as c-Met expression and Akt phosphorylation downstream from hepatocyte growth factor (HGF) or epidermal growth factor (EGF) stimulation. 21602881 2011
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease LHGDN Furthermore, the introduction of PKC-betaII suppressed HGF-induced activation of PI3K, and attenuated the in vitro invasion activity of the melanoma cells. 17625596 2008
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE We also showed Rap1 and ERK activation by both hepatocyte growth factor (HGF) and 8CPT-2Me-cAMP (an activator of Epac, a Rap1 guanine nucleotide exchange factor) in two human melanoma cell lines. 16912161 2006
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE Finally, dominant-negative inhibition of Mitf resulted in profound resistance of melanocytes and melanoma cells to HGF-dependent matrix invasion, suggesting a physiologic role for this pathway in melanocytic development and melanoma. 16455654 2006
CUI: C0025202
Disease: melanoma
melanoma
0.100 AlteredExpression disease LHGDN We report that hepatocyte growth factor/scatter factor (HGF) induces fibronectin expression and its extracellular assembly on the surface of melanoma cells through activation of mitogen-activated protein (MAP) kinase pathway, and induction and transcriptional activation of Early growth response-1 (Egr-1). 15608673 2005
CUI: C0025202
Disease: melanoma
melanoma
0.100 Biomarker disease BEFREE Recently, we reported that hepatocyte growth factor/scatter factor (HGF/SF)-transgenic mice develop melanomas after a single erythemal dose of neonatal UV radiation, supporting epidemiological data implicating childhood sunburn in CMM. 12438273 2002