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http://purl.uniprot.org/citations/24239348http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/24239348http://www.w3.org/2000/01/rdf-schema#comment"A fundamental limitation in devising new therapeutic strategies for killing cancer cells with DNA damaging agents is the need to identify synthetic lethal interactions between tumor-specific mutations and components of the DNA damage response (DDR) in vivo. The stress-activated p38 mitogen-activated protein kinase (MAPK)/MAPKAP kinase-2 (MK2) pathway is a critical component of the DDR network in p53-deficient tumor cells in vitro. To explore the relevance of this pathway for cancer therapy in vivo, we developed a specific gene targeting strategy in which Cre-mediated recombination simultaneously creates isogenic MK2-proficient and MK2-deficient tumors within a single animal. This allows direct identification of MK2 synthetic lethality with mutations that promote tumor development or control response to genotoxic treatment. In an autochthonous model of non-small-cell lung cancer (NSCLC), we demonstrate that MK2 is responsible for resistance of p53-deficient tumors to cisplatin, indicating synthetic lethality between p53 and MK2 can successfully be exploited for enhanced sensitization of tumors to DNA-damaging chemotherapeutics in vivo."xsd:string
http://purl.uniprot.org/citations/24239348http://purl.org/dc/terms/identifier"doi:10.1016/j.celrep.2013.10.025"xsd:string
http://purl.uniprot.org/citations/24239348http://purl.uniprot.org/core/author"Kim J.S."xsd:string
http://purl.uniprot.org/citations/24239348http://purl.uniprot.org/core/author"Yaffe M.B."xsd:string
http://purl.uniprot.org/citations/24239348http://purl.uniprot.org/core/author"Jacks T."xsd:string
http://purl.uniprot.org/citations/24239348http://purl.uniprot.org/core/author"Reinhardt H.C."xsd:string
http://purl.uniprot.org/citations/24239348http://purl.uniprot.org/core/author"Cannell I.G."xsd:string
http://purl.uniprot.org/citations/24239348http://purl.uniprot.org/core/author"Morandell S."xsd:string
http://purl.uniprot.org/citations/24239348http://purl.uniprot.org/core/author"Mitra T."xsd:string
http://purl.uniprot.org/citations/24239348http://purl.uniprot.org/core/author"Couvillon A.D."xsd:string
http://purl.uniprot.org/citations/24239348http://purl.uniprot.org/core/author"Ruf D.M."xsd:string
http://purl.uniprot.org/citations/24239348http://purl.uniprot.org/core/date"2013"xsd:gYear
http://purl.uniprot.org/citations/24239348http://purl.uniprot.org/core/name"Cell Rep"xsd:string
http://purl.uniprot.org/citations/24239348http://purl.uniprot.org/core/pages"868-877"xsd:string
http://purl.uniprot.org/citations/24239348http://purl.uniprot.org/core/title"A reversible gene-targeting strategy identifies synthetic lethal interactions between MK2 and p53 in the DNA damage response in vivo."xsd:string
http://purl.uniprot.org/citations/24239348http://purl.uniprot.org/core/volume"5"xsd:string
http://purl.uniprot.org/citations/24239348http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/24239348
http://purl.uniprot.org/citations/24239348http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/24239348
http://purl.uniprot.org/uniprot/#_A0A087WSN7-mappedCitation-24239348http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/24239348
http://purl.uniprot.org/uniprot/#_A0A0N4SVY1-mappedCitation-24239348http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/24239348
http://purl.uniprot.org/uniprot/#_Q0VDV7-mappedCitation-24239348http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/24239348
http://purl.uniprot.org/uniprot/#_A0A158SIS7-mappedCitation-24239348http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/24239348
http://purl.uniprot.org/uniprot/#_A0A5Q0MU23-mappedCitation-24239348http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/24239348
http://purl.uniprot.org/uniprot/#_A0A1W2P7V9-mappedCitation-24239348http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/24239348