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http://purl.uniprot.org/citations/27086779http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/27086779http://www.w3.org/2000/01/rdf-schema#comment"BACKGROUND HDAC1 has been shown to be closely associated with the occurrence of tumors. We aimed to investigate the effects of siRNA-mediated HDAC1 knockdown on the biological behavior of esophageal carcinoma cell lines. MATERIAL AND METHODS HDAC1 expression in esophageal cancer cell lines TE-1, Eca109, and EC9706 was compared by Western blot analysis. These cells were transfected with siRNA-HDAC1 and cell proliferation was evaluated by MTT assay to select the optimum cell line for subsequent experiments. The effects of siRNA-HDAC1 on the migration and invasion of the selected cell line were assessed by transwell assay. The expression of cell cycle-related proteins cyclinD1, p21 and p27, and epithelial-mesenchymal transition (EMT)-related protein zonula occludens-1 (ZO-1), E-cadherin and vimentin was determined by Western blot analysis. RESULTS HDAC1 expression in TE-1, Eca109 and EC9706 cells was significantly higher compared with normal esophageal cell line HEEC (P<0.01). MTT assay, Western blot and RT-PCR analyses demonstrated that the inhibitory effects of siRNA on HDAC1 expression and cell viability in TE-1 cells were the highest among all cell lines, which was therefore used in subsequent experiments. After TE-1 cells were transfected with siRNA-HDAC1, their migration and invasion were significantly lower compared with the controls (P<0.01). CyclinD1 and vimentin expression was significantly lower compared with the controls (P<0.01), whereas the expression of p21, p27, ZO-1 and E-cadherin was significantly higher (P<0.01). CONCLUSIONS The siRNA-mediated HDAC1 knockdown significantly inhibited the proliferation, migration and invasion of TE-1 cells probably by regulating the expression of cell cycle- and EMT-related proteins."xsd:string
http://purl.uniprot.org/citations/27086779http://purl.org/dc/terms/identifier"doi:10.12659/msm.895853"xsd:string
http://purl.uniprot.org/citations/27086779http://purl.uniprot.org/core/author"Guo H."xsd:string
http://purl.uniprot.org/citations/27086779http://purl.uniprot.org/core/author"Liu W."xsd:string
http://purl.uniprot.org/citations/27086779http://purl.uniprot.org/core/author"Wang D."xsd:string
http://purl.uniprot.org/citations/27086779http://purl.uniprot.org/core/author"Wang X."xsd:string
http://purl.uniprot.org/citations/27086779http://purl.uniprot.org/core/author"Yang L."xsd:string
http://purl.uniprot.org/citations/27086779http://purl.uniprot.org/core/author"Wang X.'"xsd:string
http://purl.uniprot.org/citations/27086779http://purl.uniprot.org/core/author"Yang C."xsd:string
http://purl.uniprot.org/citations/27086779http://purl.uniprot.org/core/date"2016"xsd:gYear
http://purl.uniprot.org/citations/27086779http://purl.uniprot.org/core/name"Med Sci Monit"xsd:string
http://purl.uniprot.org/citations/27086779http://purl.uniprot.org/core/pages"1291-1296"xsd:string
http://purl.uniprot.org/citations/27086779http://purl.uniprot.org/core/title"Effects of siRNA-Mediated Knockdown of HDAC1 on the Biological Behavior of Esophageal Carcinoma Cell Lines."xsd:string
http://purl.uniprot.org/citations/27086779http://purl.uniprot.org/core/volume"22"xsd:string
http://purl.uniprot.org/citations/27086779http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/27086779
http://purl.uniprot.org/citations/27086779http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/27086779
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http://purl.uniprot.org/uniprot/#_B4DRG0-mappedCitation-27086779http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/27086779
http://purl.uniprot.org/uniprot/#_B5BU61-mappedCitation-27086779http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/27086779
http://purl.uniprot.org/uniprot/#_B5MGH2-mappedCitation-27086779http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/27086779
http://purl.uniprot.org/uniprot/#_Q13547-mappedCitation-27086779http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/27086779
http://purl.uniprot.org/uniprot/#_Q5HYD4-mappedCitation-27086779http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/27086779
http://purl.uniprot.org/uniprot/#_Q6IT96-mappedCitation-27086779http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/27086779