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Photonic modulation of epidermal growth factor receptor halts receptor activation and cancer cell migration
Authors:Cláudia M. Botelho  Odete Gonçalves  Rogério Marques  Viruthachalam Thiagarajan  Henrik Vorum  Andreia C. Gomes  Maria Teresa Neves‐Petersen
Affiliation:1. Centre of Biological Engineering, Universidade do Minho, Braga, Portugal;2. Centre of Molecular and Environmental Biology (CBMA), Universidade do Minho, Braga, Portugal;3. Department of Health Science and Technology, Aalborg University, Aalborg, Denmark;4. International Iberian Nanotechnology Laboratory (INL), P‐4715‐310 Braga, Portugal;5. School of Chemistry, Bharathidasan University, Tiruchirappalli, India;6. Department of Clinical Medicine, Aalborg University Hospital, Aalborg, Denmark
Abstract:Epidermal growth factor receptor (EGFR) plays a key role in regulating cell survival, proliferation and migration, and its overexpression and activation has been correlated with cancer progression. Cancer therapies targeting EGFR have been applied in the clinic with some success. We show, by confocal microscopy analysis, that illumination of adenocarcinomic human alveolar basal epithelial cells (Human A549—EGFR biosensor cell line) with 280 nm at irradiance levels up to 20 times weaker than the Ultraviolet B (UVB) solar output for short periods of time (15‐45 minutes) prevents epidermal growth factor‐mediated activation of EGFR located on the cell membrane, preventing or reducing cellular disaggregation, formation of filopodia and cell migration. This effect of Ultraviolet (UV) light illumination was confirmed further in a functional scratch assay, and shown to be more effective than that of a specific EGFR‐signaling inhibitor. This new photonic approach may be applicable to the treatment of various types of cancer, alone or in combination with other therapies. image
Keywords:arrest cancer cell migration  EGF  EGFR  metastasis  photonic cancer therapy  protein photochemistry
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