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http://purl.uniprot.org/citations/29448250http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/29448250http://www.w3.org/2000/01/rdf-schema#comment"

Background/aims

Lymphocyte antigen 6 complex, locus E (LY6E) is a member of the lymphostromal cell membrane Ly6 superfamily protein. The present study investigated the clinical significance and potential biological function of LY6E in gastric cancer (GC).

Methods

LY6E mRNA and protein expressions in human GC tissues and GC cells were tested. Relationship between LY6E expression and the GC patients' clinicopathologic characteristics was analyzed. LY6E was silenced by siRNA in the cultured GC cells.

Results

The RNA expression microarray profiling assay results demonstrated that LY6E mRNA was significantly increased in multiple human GC tumor tissues. Immunohistochemistry (IHC) staining analysis revealed that 59 of 75 (78.7%) GC specimens were LY6E positive. LY6E over-expression in human GC was correlated with the histology grade, AJCC stage, N classification, lymphatic invasion, and tumor location. Notably, functional LY6E expression was also detected in AGS and other established GC cell lines. LY6E knockdown by targeted-siRNA inhibited AGS cell survival and proliferation. Meanwhile, the LY6E siRNA induced G1-S cell cycle arrest and apoptosis in AGC cells. Additionally, AGC cell migration was also inhibited by LY6E knockdown. Expressions of tumor-suppressing proteins, including PTEN (phosphatase and tensin homolog) and E-Cadherin, were increased in LY6E-silenced AGS cells.

Conclusion

LY6E over-expression in GC is potentially required for cancer cell survival, proliferation and migration."xsd:string
http://purl.uniprot.org/citations/29448250http://purl.org/dc/terms/identifier"doi:10.1159/000487453"xsd:string
http://purl.uniprot.org/citations/29448250http://purl.uniprot.org/core/author"Chen Z."xsd:string
http://purl.uniprot.org/citations/29448250http://purl.uniprot.org/core/author"Cao C."xsd:string
http://purl.uniprot.org/citations/29448250http://purl.uniprot.org/core/author"Lv Y."xsd:string
http://purl.uniprot.org/citations/29448250http://purl.uniprot.org/core/author"Jiang Q."xsd:string
http://purl.uniprot.org/citations/29448250http://purl.uniprot.org/core/author"Song Y."xsd:string
http://purl.uniprot.org/citations/29448250http://purl.uniprot.org/core/author"Shi X."xsd:string
http://purl.uniprot.org/citations/29448250http://purl.uniprot.org/core/author"Wang S."xsd:string
http://purl.uniprot.org/citations/29448250http://purl.uniprot.org/core/author"Zuo Y."xsd:string
http://purl.uniprot.org/citations/29448250http://purl.uniprot.org/core/author"Ni C."xsd:string
http://purl.uniprot.org/citations/29448250http://purl.uniprot.org/core/date"2018"xsd:gYear
http://purl.uniprot.org/citations/29448250http://purl.uniprot.org/core/name"Cell Physiol Biochem"xsd:string
http://purl.uniprot.org/citations/29448250http://purl.uniprot.org/core/pages"1219-1229"xsd:string
http://purl.uniprot.org/citations/29448250http://purl.uniprot.org/core/title"Overexpression of Lymphocyte Antigen 6 Complex, Locus E in Gastric Cancer Promotes Cancer Cell Growth and Metastasis."xsd:string
http://purl.uniprot.org/citations/29448250http://purl.uniprot.org/core/volume"45"xsd:string
http://purl.uniprot.org/citations/29448250http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/29448250
http://purl.uniprot.org/citations/29448250http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/29448250
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http://purl.uniprot.org/uniprot/Q7Z787http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/29448250
http://purl.uniprot.org/uniprot/Q16553http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/29448250