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http://purl.uniprot.org/citations/21410323http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/21410323http://www.w3.org/2000/01/rdf-schema#comment"The estrogen receptor (ER) is a primary target for breast cancer (BC) treatment. As BC progresses to estrogen-independent growth, the insulin-like growth factor-1 receptor (IGF-1R) and the ER interact in synergistic cross-talk mechanisms, which result in enhanced activation of both receptors' signaling cascades. Insulin-like growth factor-2 (IGF-2) is critical in BC progression and its actions are mediated by the IGF-1R. Our previous studies showed that IGF-2 regulates survival genes that protect the mitochondria and promote chemoresistance. In this study, we analyzed BC cells by subcellular fractionation, Western-Blot, qRT-PCR, and siRNA analysis. Our results demonstrate that IGF-2 activates ER-α and ER-β, and modulates their translocation to the nucleus, membrane organelles, and the mitochondria. IGF-2 actions are mediated by the IGF-1R and the insulin receptor. This novel mechanism of IGF-2 synergistic cross-talk signaling with ER-α and ER-β can promote estrogen-independent BC progression and provide new therapeutic targets for the treatment of BC patients."xsd:string
http://purl.uniprot.org/citations/21410323http://purl.org/dc/terms/identifier"doi:10.3109/08977194.2011.565003"xsd:string
http://purl.uniprot.org/citations/21410323http://purl.uniprot.org/core/author"Davis W."xsd:string
http://purl.uniprot.org/citations/21410323http://purl.uniprot.org/core/author"Richardson A.E."xsd:string
http://purl.uniprot.org/citations/21410323http://purl.uniprot.org/core/author"Brito C."xsd:string
http://purl.uniprot.org/citations/21410323http://purl.uniprot.org/core/author"Hamilton N."xsd:string
http://purl.uniprot.org/citations/21410323http://purl.uniprot.org/core/author"De Leon D."xsd:string
http://purl.uniprot.org/citations/21410323http://purl.uniprot.org/core/date"2011"xsd:gYear
http://purl.uniprot.org/citations/21410323http://purl.uniprot.org/core/name"Growth Factors"xsd:string
http://purl.uniprot.org/citations/21410323http://purl.uniprot.org/core/pages"82-93"xsd:string
http://purl.uniprot.org/citations/21410323http://purl.uniprot.org/core/title"Insulin-like growth factor-2 (IGF-2) activates estrogen receptor-alpha and -beta via the IGF-1 and the insulin receptors in breast cancer cells."xsd:string
http://purl.uniprot.org/citations/21410323http://purl.uniprot.org/core/volume"29"xsd:string
http://purl.uniprot.org/citations/21410323http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/21410323
http://purl.uniprot.org/citations/21410323http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/21410323
http://purl.uniprot.org/uniprot/#_A0A125SXW0-mappedCitation-21410323http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/21410323
http://purl.uniprot.org/uniprot/#_A0A125SXW1-mappedCitation-21410323http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/21410323
http://purl.uniprot.org/uniprot/#_Q14268-mappedCitation-21410323http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/21410323
http://purl.uniprot.org/uniprot/#_A0A125SXV8-mappedCitation-21410323http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/21410323
http://purl.uniprot.org/uniprot/#_A0A125SXV9-mappedCitation-21410323http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/21410323
http://purl.uniprot.org/uniprot/#_A0A125SXW2-mappedCitation-21410323http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/21410323
http://purl.uniprot.org/uniprot/#_A0A125SXW3-mappedCitation-21410323http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/21410323
http://purl.uniprot.org/uniprot/#_B0FJM0-mappedCitation-21410323http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/21410323
http://purl.uniprot.org/uniprot/#_B6DU68-mappedCitation-21410323http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/21410323
http://purl.uniprot.org/uniprot/#_B6DU69-mappedCitation-21410323http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/21410323