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http://purl.uniprot.org/citations/19839049http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/19839049http://www.w3.org/2000/01/rdf-schema#comment"The conversion of early stage tumors into invasive malignancies with an aggressive phenotype has been associated with the irreversible loss of E-cadherin expression. The loss of E-cadherin expression in human tumors, including breast cancer, has been attributed to promoter CpG island hypermethylation and direct inhibition by transcriptional repressors. Recent evidence demonstrates that up-regulation of E-cadherin by microRNA-200b (miR-200b) and miR-200c through direct targeting of transcriptional repressors of E-cadherin, ZEB1, and ZEB2, inhibits epithelial-to-mesenchymal transition (EMT), a crucial process in the tumor progression. We demonstrate that microRNA miR-200 family-mediated transcriptional up-regulation of E-cadherin in mesenchymal MDA-MB-231 and BT-549 cells is associated directly with translational repression of ZEB1 and indirectly with increased acetylation of histone H3 at the E-cadherin promoter. The increase in histone H3 acetylation may be attributed to the disruption of repressive complexes between ZEB1 and histone deacetylases and to the inhibition of SIRT1, a class III histone deacetylase. These events inhibit EMT and reactivate a less aggressive epithelial phenotype in cancer cells. Additionally, disruption of ZEB1-histone deacetylase repressor complexes and down-regulation of SIRT1 histone deacetylase up-regulate proapoptotic genes in the p53 apoptotic pathway resulting in the increased sensitivity of cancer cells to the chemotherapeutic agent doxorubicin."xsd:string
http://purl.uniprot.org/citations/19839049http://purl.org/dc/terms/identifier"doi:10.1002/ijc.24972"xsd:string
http://purl.uniprot.org/citations/19839049http://purl.uniprot.org/core/author"Pogribny I.P."xsd:string
http://purl.uniprot.org/citations/19839049http://purl.uniprot.org/core/author"Tryndyak V.P."xsd:string
http://purl.uniprot.org/citations/19839049http://purl.uniprot.org/core/author"Beland F.A."xsd:string
http://purl.uniprot.org/citations/19839049http://purl.uniprot.org/core/date"2010"xsd:gYear
http://purl.uniprot.org/citations/19839049http://purl.uniprot.org/core/name"Int J Cancer"xsd:string
http://purl.uniprot.org/citations/19839049http://purl.uniprot.org/core/pages"2575-2583"xsd:string
http://purl.uniprot.org/citations/19839049http://purl.uniprot.org/core/title"E-cadherin transcriptional down-regulation by epigenetic and microRNA-200 family alterations is related to mesenchymal and drug-resistant phenotypes in human breast cancer cells."xsd:string
http://purl.uniprot.org/citations/19839049http://purl.uniprot.org/core/volume"126"xsd:string
http://purl.uniprot.org/citations/19839049http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/19839049
http://purl.uniprot.org/citations/19839049http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/19839049
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http://purl.uniprot.org/uniprot/#_P12830-mappedCitation-19839049http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/19839049
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