Abstract | BACKGROUND/AIM: Lewis y is expressed in oral squamous cell carcinoma (OSCC) cells and tumors. Previously, we reported that Lewis y was not expressed in invasion areas, and attenuation of proliferation and invasion in OSCC cells was caused by over-expression of Lewis y. However, the roles of Lewis y in the attenuation of malignant properties have not been clarified. In this study, we investigated the roles of Lewis y in OSCC. MATERIALS AND METHODS: The levels of Lewis y on EGFR and the phosphorylation levels of EGFR in OSCC cells were analyzed by immunoprecipitation and western blot. EGFR cross-linking and binding kinetics of EGF were performed. RESULTS: Upon EGF stimulation, phosphorylation and dimer formation of EGFR were more prominent in Lewis y- cells. EGF binding kinetics showed reduced binding sites in Lewis y+ cells. CONCLUSION: Lewis y reduced EGF binding to EGFR, leading to suppression of malignant properties through suppression of EGF signaling.
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Authors | Hiroshi Hotta, Kazunori Hamamura, Hidenobu Shibuya, Yuhsuke Ohmi, Keiko Furukawa, Koichi Furukawa |
Journal | Anticancer research
(Anticancer Res)
Vol. 41
Issue 4
Pg. 1821-1830
(Apr 2021)
ISSN: 1791-7530 [Electronic] Greece |
PMID | 33813387
(Publication Type: Journal Article)
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Copyright | Copyright © 2021 International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved. |
Chemical References |
- Lewis Blood Group Antigens
- Lewis Y antigen
- Epidermal Growth Factor
- EGFR protein, human
- ErbB Receptors
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Topics |
- Binding Sites
- Cell Adhesion
- Cell Line, Tumor
- Cell Movement
- Cell Shape
- Epidermal Growth Factor
(metabolism)
- ErbB Receptors
(metabolism)
- Humans
- Kinetics
- Lewis Blood Group Antigens
(metabolism)
- Mouth Neoplasms
(metabolism, pathology)
- Neoplasm Invasiveness
- Phosphorylation
- Protein Binding
- Signal Transduction
- Squamous Cell Carcinoma of Head and Neck
(metabolism, pathology)
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