http://purl.uniprot.org/citations/24103454 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Journal_Citation |
http://purl.uniprot.org/citations/24103454 | http://www.w3.org/2000/01/rdf-schema#comment | "BackgroundmicroRNAs have been shown to regulate the chemosensitivity of cancer cells. The aim of this study is to investigate the role and mechanism of mir-23a in enhancing the anti-tumor effect of topoisomerase 2A (TOP2A) poison etoposide in human hepatocellular carcinoma (HCC).MethodsThe anti-tumor effect of chemotherapeutic agents in HCC cells were examined in vitro and in vivo xenograft model. Expression of mRNA and miRNAs were determined by quantitative real-time PCR. Protein expression was analyzed by immunoblotting.ResultsOverexpression of mir-23a could significantly potentiate the in vitro and in vivo anti-tumor effect of etoposide; however, ectopic expression of miR-23a fails to sensitize HCC cells to 5-fluorouracil treatment, indicating the miR-23a-induced cancer cell hypersensitivity in chemotherapy is TOP2A-specific though miR-23a overexpression could not directly up-regulate TOP2A expression. Topoisomerase 1(TOP1) is down-regulated in miR-23a-overexpressed HCC cells. MiR-23a could directly bind to 3'untranslated region of TOP1 mRNA, and suppress the corresponding protein expression and inhibition of miR-23a further arguments the expression of TOP1. MiR-23a was up-regulated during DNA damage in cancer cells in line with the p53 expression. Up-regulation of p53 induces mir-23a expression, while suppression of p53 inhibits miR-23a in HCC cells.ConclusionOur study sheds light on the role of miR-23a as a potential target in regulating chemosensitivity of HCC cells."xsd:string |
http://purl.uniprot.org/citations/24103454 | http://purl.org/dc/terms/identifier | "doi:10.1186/1476-4598-12-119"xsd:string |
http://purl.uniprot.org/citations/24103454 | http://purl.uniprot.org/core/author | "Feng Y."xsd:string |
http://purl.uniprot.org/citations/24103454 | http://purl.uniprot.org/core/author | "Zhang Z."xsd:string |
http://purl.uniprot.org/citations/24103454 | http://purl.uniprot.org/core/author | "Tsao S.W."xsd:string |
http://purl.uniprot.org/citations/24103454 | http://purl.uniprot.org/core/author | "Wang N."xsd:string |
http://purl.uniprot.org/citations/24103454 | http://purl.uniprot.org/core/author | "Zhu M."xsd:string |
http://purl.uniprot.org/citations/24103454 | http://purl.uniprot.org/core/author | "Man K."xsd:string |
http://purl.uniprot.org/citations/24103454 | http://purl.uniprot.org/core/date | "2013"xsd:gYear |
http://purl.uniprot.org/citations/24103454 | http://purl.uniprot.org/core/name | "Mol Cancer"xsd:string |
http://purl.uniprot.org/citations/24103454 | http://purl.uniprot.org/core/pages | "119"xsd:string |
http://purl.uniprot.org/citations/24103454 | http://purl.uniprot.org/core/title | "MiR-23a-mediated inhibition of topoisomerase 1 expression potentiates cell response to etoposide in human hepatocellular carcinoma."xsd:string |
http://purl.uniprot.org/citations/24103454 | http://purl.uniprot.org/core/volume | "12"xsd:string |
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