2010Medical Journal of West ChinaRequires access

Effects of S1P5 on adhesion of human esophageal cancer cell line Eca109

Tang En-jie

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Abstract

Objective To investigate the effect of S1P5 on adhesion of human esophageal squamous cell carcinoma(ESCC) cell line Eca109.Methods Human S1P5 gene was cloned from normal esophageal mucosal epithelium.S1P5-EGFP vector was constructed and transfected into Eca109 cells.The S1P5 expressing Eca109 cell was designated S1P5-EGFP/Eca109.With Control-EGFP vector transfecting Eca109 cell as control,cell morphology and adhesion were analyzed by fluorescence microscopy and cell adhesion assay,respectively.Results S1P5-EGFP and Control-EGFP vectors,and their corresponding stably-transfected Eca109 cells were successfully constructed.S1P5 overexpressing Eca109 cells displayed spindle cell morphology and S1P5 was expressed on the plasma membrane.The cell adhesion of S1P5-transfected Eca109 cells was lower than control vector-transfected cells with or without sphingosine 1-phosphate(P0.05).Conclusion The data demonstrate that S1P5 constitutively inhibits Eca109 cell adhesion.Esophageal cancer cells may down-regulate the expression of S1P5 to promote adhesion.

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Objective To investigate the effect of S1P5 on adhesion of human esophageal squamous cell carcinoma(ESCC) cell line Eca109.Methods Human S1P5 gene was cloned from normal esophageal mucosal epithelium.S1P5-EGFP vector was constructed and transfected into Eca109 cells.The S1P5 expressing Eca109 cell was designated S1P5-EGFP/Eca109.With Control-EGFP vector transfecting Eca109 cell as control,cell morphology and adhesion were analyzed by fluorescence microscopy and cell adhesion assay,respectively.Results S1P5-EGFP and Control-EGFP vectors,and their corresponding stably-transfected Eca109 cells were successfully constructed.S1P5 overexpressing Eca109 cells displayed spindle cell morphology and S1P5 was expressed on the plasma membrane.The cell adhesion of S1P5-transfected Eca109 cells was lower than control vector-transfected cells with or without sphingosine 1-phosphate(P0.05).Conclusion The data demonstrate that S1P5 constitutively inhibits Eca109 cell adhesion.Esophageal cancer cells may down-regulate the expression of S1P5 to promote adhesion.

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Available abstract

Objective To investigate the effect of S1P5 on adhesion of human esophageal squamous cell carcinoma(ESCC) cell line Eca109.Methods Human S1P5 gene was cloned from normal esophageal mucosal epithelium.S1P5-EGFP vector was constructed and transfected into Eca109 cells.The S1P5 expressing Eca109 cell was designated S1P5-EGFP/Eca109.With Control-EGFP vector transfecting Eca109 cell as control,cell morphology and adhesion were analyzed by fluorescence microscopy and cell adhesion assay,respectively.Results S1P5-EGFP and Control-EGFP vectors,and their corresponding stably-transfected Eca109 cells were successfully constructed.S1P5 overexpressing Eca109 cells displayed spindle cell morphology and S1P5 was expressed on the plasma membrane.The cell adhesion of S1P5-transfected Eca109 cells was lower than control vector-transfected cells with or without sphingosine 1-phosphate(P0.05).Conclusion The data demonstrate that S1P5 constitutively inhibits Eca109 cell adhesion.Esophageal cancer cells may down-regulate the expression of S1P5 to promote adhesion.

Key concepts: Transfection, Adhesion, Cell adhesion, Cell, Cell culture, Molecular biology, Cell biology, Medicine

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