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http://purl.uniprot.org/citations/26311513http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/26311513http://www.w3.org/2000/01/rdf-schema#comment"Although invasive and metastatic progression via the epithelial-mesenchymal transition (EMT) and acquisition of resistance to castration are both critical steps in prostate cancer, the molecular mechanism of this interaction remains unclear. In this study, we aimed to elucidate the interaction of signaling between castration resistance and EMT, and to apply this information to the development of a novel therapeutic concept using transforming growth factor-β (TGF-β) inhibitor SB525334 combined with androgen-deprivation therapy against prostate cancer using an in vivo model. This study revealed that an EMT inducer (TGF-β) induced full-length androgen receptor (AR) and AR variant expression. In addition, a highly invasive clone showed augmented full-length AR and AR variant expression as well as acquisition of castration resistance. Conversely, full-length AR and AR as well as Twist1 and mesenchymal molecules variant expression were up-regulated in castration-resistant LNCaP xenograft. Finally, TGF-β inhibitor suppressed Twist1 and AR expression as well as prostate cancer growth combined with castration. Taken together, these results demonstrate that Twist1/AR signaling was augmented in castration resistant as well as mesenchymal-phenotype prostate cancer, indicating the molecular mechanism of mutual and functional crosstalk between EMT and castration resistance, which may play a crucial role in prostate carcinogenesis and progression."xsd:string
http://purl.uniprot.org/citations/26311513http://purl.org/dc/terms/identifier"doi:10.1530/erc-15-0225"xsd:string
http://purl.uniprot.org/citations/26311513http://purl.uniprot.org/core/author"Imada K."xsd:string
http://purl.uniprot.org/citations/26311513http://purl.uniprot.org/core/author"Oda Y."xsd:string
http://purl.uniprot.org/citations/26311513http://purl.uniprot.org/core/author"Uchiumi T."xsd:string
http://purl.uniprot.org/citations/26311513http://purl.uniprot.org/core/author"Takeuchi A."xsd:string
http://purl.uniprot.org/citations/26311513http://purl.uniprot.org/core/author"Naito S."xsd:string
http://purl.uniprot.org/citations/26311513http://purl.uniprot.org/core/author"Inokuchi J."xsd:string
http://purl.uniprot.org/citations/26311513http://purl.uniprot.org/core/author"Yokomizo A."xsd:string
http://purl.uniprot.org/citations/26311513http://purl.uniprot.org/core/author"Shiota M."xsd:string
http://purl.uniprot.org/citations/26311513http://purl.uniprot.org/core/author"Itsumi M."xsd:string
http://purl.uniprot.org/citations/26311513http://purl.uniprot.org/core/author"Kuruma H."xsd:string
http://purl.uniprot.org/citations/26311513http://purl.uniprot.org/core/author"Tatsugami K."xsd:string
http://purl.uniprot.org/citations/26311513http://purl.uniprot.org/core/date"2015"xsd:gYear
http://purl.uniprot.org/citations/26311513http://purl.uniprot.org/core/name"Endocr Relat Cancer"xsd:string
http://purl.uniprot.org/citations/26311513http://purl.uniprot.org/core/pages"889-900"xsd:string
http://purl.uniprot.org/citations/26311513http://purl.uniprot.org/core/title"Crosstalk between epithelial-mesenchymal transition and castration resistance mediated by Twist1/AR signaling in prostate cancer."xsd:string
http://purl.uniprot.org/citations/26311513http://purl.uniprot.org/core/volume"22"xsd:string
http://purl.uniprot.org/citations/26311513http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/26311513
http://purl.uniprot.org/citations/26311513http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/26311513
http://purl.uniprot.org/uniprot/#_Q15672-mappedCitation-26311513http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/26311513
http://purl.uniprot.org/uniprot/Q15672http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/26311513