NRAS, NRAS proto-oncogene, GTPase, 4893

N. diseases: 611; N. variants: 17
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0025202
Disease: melanoma
melanoma
0.700 GeneticVariation disease BEFREE Furthermore, no effective targeted therapy has been developed for NRAS mutant tumors or in melanomas with as yet unknown driver mutations. 23420410 2013
CUI: C0025202
Disease: melanoma
melanoma
0.700 CausalMutation disease CLINVAR Combined targeting of MEK and PI3K/mTOR effector pathways is necessary to effectively inhibit NRAS mutant melanoma in vitro and in vivo. 23431193 2013
CUI: C0025202
Disease: melanoma
melanoma
0.700 GeneticVariation disease BEFREE Isocitrate dehydrogenase 1 mutations in melanoma frequently co-occur with NRAS mutations. 30003571 2018
CUI: C0025202
Disease: melanoma
melanoma
0.700 GeneticVariation disease BEFREE In conclusion, our findings show miRNA dysregulation in malignant melanoma and its relation to established molecular backgrounds of BRAF and NRAS oncogenic mutations. 20357817 2010
CUI: C0025202
Disease: melanoma
melanoma
0.700 GeneticVariation disease BEFREE No mutations of the BRAF and NRAS genes were found in the melanoma. 19264228 2009
CUI: C0025202
Disease: melanoma
melanoma
0.700 AlteredExpression disease BEFREE We found that the RICTOR locus is frequently amplified and overexpressed in melanoma and that RICTOR over-expression in NRAS-transformed melanocytes stimulates their clonogenicity, demonstrating that RICTOR amplification can cooperate with NRAS mutation to stimulate melanoma proliferation. 26356562 2015
CUI: C0025202
Disease: melanoma
melanoma
0.700 GeneticVariation disease BEFREE No significant differences in the distribution of BRAF or NRAS mutations could be found between melanoma and associated nevi or between melanoma associated nevi and control nevi. 23861977 2013
CUI: C0025202
Disease: melanoma
melanoma
0.700 GeneticVariation disease BEFREE Mutations in the ras genes are key events in the process of carcinogenesis; in particular, point mutations in codon 61 of exon 2 of the N-ras gene occur frequently in cutaneous melanoma. 11886512 2001
CUI: C0025202
Disease: melanoma
melanoma
0.700 GeneticVariation disease BEFREE Melanoma onset and progression are associated with a high variety of activating mutations in the MAPK-pathway, most frequently involving BRAF (35-45%) and NRAS (15-25%) genes, but also c-KIT and PTEN. 31446019 2019
CUI: C0025202
Disease: melanoma
melanoma
0.700 CausalMutation disease CLINVAR Inhibition of Wee1, AKT, and CDK4 underlies the efficacy of the HSP90 inhibitor XL888 in an in vivo model of NRAS-mutant melanoma. 23538902 2013
CUI: C0025202
Disease: melanoma
melanoma
0.700 GeneticVariation 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
0.700 Biomarker disease BEFREE Methods Patients with HNPCC with a diagnosis of MM were studied by immunohistochemistry (IHC) on tumour tissue using antibodies to MLH1, MSH2, p16, beta-catenin and E-cadherin, and by direct sequencing of MMR genes on germline DNA, and BRAF and NRAS on somatic DNA extracted from MM. 18460031 2008
CUI: C0025202
Disease: melanoma
melanoma
0.700 GeneticVariation disease BEFREE We analyzed exons 1, 11, and 15 of the BRAF gene and exons 1 and 2 of the N-ras gene for mutations in 38 metastatic melanomas by PCR-single-strand conformation polymorphism and direct sequencing. 12960123 2003
CUI: C0025202
Disease: melanoma
melanoma
0.700 GeneticVariation disease BEFREE Whereas many studies have analyzed RAF and PI3K signaling in mutant NRAS melanoma, the role of RalGEF/Ral is understudied and TBK1 has not been examined. 24962318 2014
CUI: C0025202
Disease: melanoma
melanoma
0.700 GeneticVariation disease BEFREE When compared to WT, multivariate analysis of melanoma-specific survival (MSS) identified NRAS mutations as an adverse prognostic factor [hazard ratio (HR) 2.96; P = 0.04] but not BRAF(V600E) mutations (HR 1.73; P = 0.23). 21615881 2011
CUI: C0025202
Disease: melanoma
melanoma
0.700 GeneticVariation disease BEFREE Selective MEK inhibitors have the ability to inhibit growth and induce cell death in BRAF- and NRAS-mutant melanoma cell lines. 28537004 2017
CUI: C0025202
Disease: melanoma
melanoma
0.700 Biomarker disease CTD_human Our analysis established NF1, encoding a negative regulator of RAS, as the third most frequently mutated gene in melanoma, after BRAF and NRAS. 26214590 2015
CUI: C0025202
Disease: melanoma
melanoma
0.700 GeneticVariation disease BEFREE BRAF and NRAS mutations were more frequent in nodular and superficial spreading melanomas (P < 0.001). 25357015 2015
CUI: C0025202
Disease: melanoma
melanoma
0.700 AlteredExpression disease BEFREE Usp9x regulates Ets-1 ubiquitination and stability to control NRAS expression and tumorigenicity in melanoma. 28198367 2017
CUI: C0025202
Disease: melanoma
melanoma
0.700 GeneticVariation disease BEFREE BRAF and NRAS mutations are predominant in melanoma and lead to overactivation of the mitogen-activated protein kinase (MAPK) and phosphatidylinositol 3-kinase (PI3K)/protein kinase B (AKT) signaling pathways. 28543695 2017
CUI: C0025202
Disease: melanoma
melanoma
0.700 GeneticVariation disease BEFREE N2/M2 lesions are characterized by inflammatory-type and AXL gene signatures with an equal distribution of wild-type and mutated BRAF and low prevalence of NRAS mutations in M2 melanomas. 29995873 2018
CUI: C0025202
Disease: melanoma
melanoma
0.700 CausalMutation disease CLINVAR Pharmacodynamic effects and mechanisms of resistance to vemurafenib in patients with metastatic melanoma. 23569304 2013
CUI: C0025202
Disease: melanoma
melanoma
0.700 GeneticVariation disease BEFREE Furthermore, we tested the impact of a second NRAS mutation in 7 BRAF inhibitor resistant early passage cell cultures on the selection of second line therapies.We observed a rapid monophyletic evolution of melanoma subpopulations in response to targeted therapy that was not observed in non-targeted therapy. 27791198 2016
CUI: C0025202
Disease: melanoma
melanoma
0.700 GeneticVariation disease BEFREE Both the melanomas harbor KIT mutation in approximately 15% of the cases; BRAF or NRAS mutation is found in approximately 10-15% of acral melanoma, but these mutations are less frequent in mucosal melanoma. 30675668 2019
CUI: C0025202
Disease: melanoma
melanoma
0.700 GeneticVariation disease BEFREE In contrast the epithelial-like subtype of melanomas with wild-type N-RAS and B-RAF alleles displayed an effective G2 checkpoint but a significant defect in G1 checkpoint function. 17597816 2008