http://purl.uniprot.org/citations/30576678 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Journal_Citation |
http://purl.uniprot.org/citations/30576678 | http://www.w3.org/2000/01/rdf-schema#comment | "Growth-arrest-specific transcript 5 (GAS5) functions as a tumor suppressor in a variety of cancers. GAS5 has been reported to be down-regulated in oral squamous cell carcinoma (OSCC). The aim of this study was to investigate the mechanisms of how GAS5 acts as a tumor suppressor in OSCC. qRT-PCR, cell viability, wound-healing, and transwell assays showed that knockdown of GAS5 increased miR-21 expression and promoted proliferation, migration, invasion, and epithelial-mesenchymal transition of OSCC cells. In contrast, overexpression of GAS5 showed the opposite effects. Furthermore, miR-21 overexpression reversed the effect of GAS5. Western blot showed that knockdown of GAS5 suppressed PTEN, while phosphorylation of Akt was promoted. PCNA, cyclinD1, and Ki-67 were up-regulated, indicating enhanced proliferation. E-cadherin was down-regulated, while N-cadherin, vimentin, and snail1 were increased, indicating augmented epithelial-mesenchymal transition. Overexpression of GAS5 regulated these proteins inversely. Overexpression of miR-21 reversed the effect of GAS5 on these proteins. Taken together, GAS5 suppresses proliferation, migration, invasion, and epithelial-mesenchymal transition in OSCC through the miR-21/PTEN axis and might be a novel therapeutic target for OSCC."xsd:string |
http://purl.uniprot.org/citations/30576678 | http://purl.org/dc/terms/identifier | "doi:10.1016/j.yexcr.2018.12.014"xsd:string |
http://purl.uniprot.org/citations/30576678 | http://purl.uniprot.org/core/author | "Chen G."xsd:string |
http://purl.uniprot.org/citations/30576678 | http://purl.uniprot.org/core/author | "Li Y."xsd:string |
http://purl.uniprot.org/citations/30576678 | http://purl.uniprot.org/core/author | "Jiang F."xsd:string |
http://purl.uniprot.org/citations/30576678 | http://purl.uniprot.org/core/author | "Zhang W."xsd:string |
http://purl.uniprot.org/citations/30576678 | http://purl.uniprot.org/core/author | "Zhao W."xsd:string |
http://purl.uniprot.org/citations/30576678 | http://purl.uniprot.org/core/author | "Yu D."xsd:string |
http://purl.uniprot.org/citations/30576678 | http://purl.uniprot.org/core/author | "Wei C."xsd:string |
http://purl.uniprot.org/citations/30576678 | http://purl.uniprot.org/core/author | "Zeng B."xsd:string |
http://purl.uniprot.org/citations/30576678 | http://purl.uniprot.org/core/date | "2019"xsd:gYear |
http://purl.uniprot.org/citations/30576678 | http://purl.uniprot.org/core/name | "Exp Cell Res"xsd:string |
http://purl.uniprot.org/citations/30576678 | http://purl.uniprot.org/core/pages | "365-373"xsd:string |
http://purl.uniprot.org/citations/30576678 | http://purl.uniprot.org/core/title | "LncRNA GAS5 suppresses proliferation, migration, invasion, and epithelial-mesenchymal transition in oral squamous cell carcinoma by regulating the miR-21/PTEN axis."xsd:string |
http://purl.uniprot.org/citations/30576678 | http://purl.uniprot.org/core/volume | "374"xsd:string |
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