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http://purl.uniprot.org/citations/16843263http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/16843263http://www.w3.org/2000/01/rdf-schema#comment"HER2/Neu gene mutations have been identified in lung cancer. Expression of a HER2 mutant containing a G776(YVMA) insertion in exon 20 was more potent than wild-type HER2 in associating with and activating signal transducers, phosphorylating EGFR, and inducing survival, invasiveness, and tumorigenicity. HER2(YVMA) transphosphorylated kinase-dead EGFR(K721R) and EGFR(WT) in the presence of EGFR tyrosine kinase inhibitors (TKIs). Knockdown of mutant HER2 in H1781 lung cancer cells increased apoptosis and restored sensitivity to EGFR TKIs. The HER2 inhibitors lapatinib, trastuzumab, and CI-1033 inhibited growth of H1781 cells and cells expressing exogenous HER2(YVMA). These data suggest that (1) HER2(YVMA) activates cellular substrates more potently than HER2(WT); and (2) cancer cells expressing this mutation remain sensitive to HER2-targeted therapies but insensitive to EGFR TKIs."xsd:string
http://purl.uniprot.org/citations/16843263http://purl.org/dc/terms/identifier"doi:10.1016/j.ccr.2006.05.023"xsd:string
http://purl.uniprot.org/citations/16843263http://purl.uniprot.org/core/author"Gazdar A.F."xsd:string
http://purl.uniprot.org/citations/16843263http://purl.uniprot.org/core/author"Yang S."xsd:string
http://purl.uniprot.org/citations/16843263http://purl.uniprot.org/core/author"Xiang B."xsd:string
http://purl.uniprot.org/citations/16843263http://purl.uniprot.org/core/author"Wang S.E."xsd:string
http://purl.uniprot.org/citations/16843263http://purl.uniprot.org/core/author"Wu F.Y."xsd:string
http://purl.uniprot.org/citations/16843263http://purl.uniprot.org/core/author"Carpenter G."xsd:string
http://purl.uniprot.org/citations/16843263http://purl.uniprot.org/core/author"Arteaga C.L."xsd:string
http://purl.uniprot.org/citations/16843263http://purl.uniprot.org/core/author"Muthuswamy S.K."xsd:string
http://purl.uniprot.org/citations/16843263http://purl.uniprot.org/core/author"Narasanna A."xsd:string
http://purl.uniprot.org/citations/16843263http://purl.uniprot.org/core/author"Perez-Torres M."xsd:string
http://purl.uniprot.org/citations/16843263http://purl.uniprot.org/core/date"2006"xsd:gYear
http://purl.uniprot.org/citations/16843263http://purl.uniprot.org/core/name"Cancer Cell"xsd:string
http://purl.uniprot.org/citations/16843263http://purl.uniprot.org/core/pages"25-38"xsd:string
http://purl.uniprot.org/citations/16843263http://purl.uniprot.org/core/title"HER2 kinase domain mutation results in constitutive phosphorylation and activation of HER2 and EGFR and resistance to EGFR tyrosine kinase inhibitors."xsd:string
http://purl.uniprot.org/citations/16843263http://purl.uniprot.org/core/volume"10"xsd:string
http://purl.uniprot.org/citations/16843263http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/16843263
http://purl.uniprot.org/citations/16843263http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/16843263
http://purl.uniprot.org/uniprot/#_P56975-mappedCitation-16843263http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/16843263
http://purl.uniprot.org/uniprot/#_Q07889-mappedCitation-16843263http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/16843263
http://purl.uniprot.org/uniprot/#_A0A8A0Y2Q6-mappedCitation-16843263http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/16843263
http://purl.uniprot.org/uniprot/#_A0A0R9RWK2-mappedCitation-16843263http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/16843263
http://purl.uniprot.org/uniprot/#_E2I6F8-mappedCitation-16843263http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/16843263