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Lewis y Expressed in Oral Squamous Cell Carcinoma Attenuates Malignant Properties via Down-regulation of EGF Signaling.

AbstractBACKGROUND/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.
AuthorsHiroshi Hotta, Kazunori Hamamura, Hidenobu Shibuya, Yuhsuke Ohmi, Keiko Furukawa, Koichi Furukawa
JournalAnticancer research (Anticancer Res) Vol. 41 Issue 4 Pg. 1821-1830 (Apr 2021) ISSN: 1791-7530 [Electronic] Greece
PMID33813387 (Publication Type: Journal Article)
CopyrightCopyright © 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
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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