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http://purl.uniprot.org/citations/29992578http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/29992578http://www.w3.org/2000/01/rdf-schema#comment"GPRC5A, a retinoic acid induced gene, is preferentially expressed in lung tissue. Gprc5a gene deletion leads to spontaneous lung tumor development. However, the mechanism of Gprc5a-mediated lung tumor suppression is not fully understood. Here we showed that MDM2, a p53-negative regulator, was dysregulated in Gprc5a-knockout (ko) mouse tracheal epithelial cells (KO-MTEC) compared to wild type ones. Targeting MDM2 in 1601-a Gprc5a-ko mouse derived lung tumor cell line-and A549-human lung cancer cells, by MDM2 inhibitor Nutlin-3a or small hairpin RNA (sh-RNA)-restored p53 signaling pathway, reduced cancer stem cell markers, and inhibited tumorigenicity. This suggests that dysregulated MDM2 pathway is essential for the oncogenic activities of these cells. MDM2 was found to be stabilized mainly by activated EGFR signaling as targeting EGFR by Erlotinib or sh-RNA repressed MDM2 in a transcription-independent manner. Importantly, overexpression of MDM2 and reduced GPRC5A expression at both protein and mRNA levels were frequently found in clinical human lung cancer tissues. Taken together, GPRC5A deficiency contributes to dysregulated MDM2 via activated EGFR signaling, which promotes lung tumor development."xsd:string
http://purl.uniprot.org/citations/29992578http://purl.org/dc/terms/identifier"doi:10.1002/ijc.31726"xsd:string
http://purl.uniprot.org/citations/29992578http://purl.uniprot.org/core/author"Hu M."xsd:string
http://purl.uniprot.org/citations/29992578http://purl.uniprot.org/core/author"Li K."xsd:string
http://purl.uniprot.org/citations/29992578http://purl.uniprot.org/core/author"Guo W."xsd:string
http://purl.uniprot.org/citations/29992578http://purl.uniprot.org/core/author"Liao Y."xsd:string
http://purl.uniprot.org/citations/29992578http://purl.uniprot.org/core/author"Sun B."xsd:string
http://purl.uniprot.org/citations/29992578http://purl.uniprot.org/core/author"Xu D."xsd:string
http://purl.uniprot.org/citations/29992578http://purl.uniprot.org/core/author"Song H."xsd:string
http://purl.uniprot.org/citations/29992578http://purl.uniprot.org/core/author"Wang T."xsd:string
http://purl.uniprot.org/citations/29992578http://purl.uniprot.org/core/author"Deng J."xsd:string
http://purl.uniprot.org/citations/29992578http://purl.uniprot.org/core/author"Yao F."xsd:string
http://purl.uniprot.org/citations/29992578http://purl.uniprot.org/core/author"Jing B."xsd:string
http://purl.uniprot.org/citations/29992578http://purl.uniprot.org/core/date"2019"xsd:gYear
http://purl.uniprot.org/citations/29992578http://purl.uniprot.org/core/name"Int J Cancer"xsd:string
http://purl.uniprot.org/citations/29992578http://purl.uniprot.org/core/pages"777-787"xsd:string
http://purl.uniprot.org/citations/29992578http://purl.uniprot.org/core/title"GPRC5A deficiency leads to dysregulated MDM2 via activated EGFR signaling for lung tumor development."xsd:string
http://purl.uniprot.org/citations/29992578http://purl.uniprot.org/core/volume"144"xsd:string
http://purl.uniprot.org/citations/29992578http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/29992578
http://purl.uniprot.org/citations/29992578http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/29992578
http://purl.uniprot.org/uniprot/#_G5E8C3-mappedCitation-29992578http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/29992578
http://purl.uniprot.org/uniprot/#_P23804-mappedCitation-29992578http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/29992578
http://purl.uniprot.org/uniprot/#_J3QP04-mappedCitation-29992578http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/29992578
http://purl.uniprot.org/uniprot/#_Q5SVE7-mappedCitation-29992578http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/29992578