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http://purl.uniprot.org/citations/34296545http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/34296545http://www.w3.org/2000/01/rdf-schema#comment"

Purpose

Eph receptors are differentially expressed in numerous malignant tumors. This study intended to analyze the roles of EphB receptors (EphB2, B3, and B4) in urinary bladder cancer.

Materials and methods

Tissue microarray-based immunohistochemical analysis was used to investigate the expression patterns of EphB2, EphB3, and EphB4 in 154 bladder cancer specimens. Immunohistochemical staining was conducted examining the extent of stained cells and staining intensity. EphB was considered to be highly expressed when the intensity of staining was more than moderate in >25% of cells in the tissue section. Small interfering RNA (siRNA) was used to knock down EphB expression in bladder cancer cell lines (T24, 5637) to determine the effects of EphB on tumor cell invasion, proliferation, and migration.

Results

EphB receptors (B2, B3, and B4) were detected in 40.9% (EphB2, 63/154), 71.4% (EphB3, 110/154), and 53.2% (EphB4, 82/154) of bladder cancer specimens. Low expression of EphB2, B3, and B4 receptors were significantly associated with higher tumor grade (EphB2, p<0.001; EphB3, p=0.032; EphB4, p<0.001) and muscular invasion (EphB2, p=0.002; EphB3, p=0.009; EphB4, p<0.001). No obvious correlation was observed with other clinicopathological variables, such as age, sex, recurrence, lymph node involvement, metastasis, and overall survival. Inactivation of EphB receptors by siRNA transfection increased cell viability, tumor cell invasion, proliferation, and migration in comparison with untransfected cancer cells.

Conclusion

Low expression of EphB receptors (B2, B3, and B4) can be a predictive marker for muscular invasion of bladder cancer."xsd:string
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http://purl.uniprot.org/citations/34296545http://purl.uniprot.org/core/author"Lee T.H."xsd:string
http://purl.uniprot.org/citations/34296545http://purl.uniprot.org/core/author"Lee G.H."xsd:string
http://purl.uniprot.org/citations/34296545http://purl.uniprot.org/core/author"Park D.S."xsd:string
http://purl.uniprot.org/citations/34296545http://purl.uniprot.org/core/author"Kim T.H."xsd:string
http://purl.uniprot.org/citations/34296545http://purl.uniprot.org/core/author"Jeong J.Y."xsd:string
http://purl.uniprot.org/citations/34296545http://purl.uniprot.org/core/author"Heo J.H."xsd:string
http://purl.uniprot.org/citations/34296545http://purl.uniprot.org/core/date"2021"xsd:gYear
http://purl.uniprot.org/citations/34296545http://purl.uniprot.org/core/name"Yonsei Med J"xsd:string
http://purl.uniprot.org/citations/34296545http://purl.uniprot.org/core/pages"679-690"xsd:string
http://purl.uniprot.org/citations/34296545http://purl.uniprot.org/core/title"Low Expression of EphB2, EphB3, and EphB4 in Bladder Cancer: Novel Potential Indicators of Muscular Invasion."xsd:string
http://purl.uniprot.org/citations/34296545http://purl.uniprot.org/core/volume"62"xsd:string
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