Inhibitory effect of blue light emitting diode on migration and invasion of cancer cells.
Phil-Sun OhHyun-Soo KimEun-Mi KimHyosook HwangHyang Hwa RyuSeokTae LimMyung-Hee SohnHwan-Jeong JeongPublished in: Journal of cellular physiology (2017)
The aim of this study was to determine the effects and molecular mechanism of blue light emitting diode (LED) in tumor cells. A migration and invasion assay for the metastatic behavior of mouse colon cancer CT-26 and human fibrosarcoma HT-1080 cells was performed. Cancer cell migration-related proteins were identified by obtaining a 2-dimensional gel electrophoresis (2-DE) in total cellular protein profile of blue LED-irradiated cancer cells, followed by matrix-assisted laser desorption/ionization-time of flight (MALDI-TOF) analysis of proteins. Protein levels were examined by immunoblotting. Irradiation with blue LED inhibited CT-26 and HT-1080 cell migration and invasion. The anti-metastatic effects of blue LED irradiation were associated with inhibition of matrix metalloproteinase (MMP)-2 and MMP-9 expression. P38 MAPK phosphorylation was increased in blue LED-irradiated CT-26 and HT-1080 cells, but was inhibited after pretreatment with SB203580, a specific inhibitor of p38 MAPK. Inhibition of p38 MAPK phosphorylation by SB203580 treatment increased number of migratory cancer cells in CT-26 and HT-1080 cells, indicating that blue LED irradiation inhibited cancer cell migration via phosphorylation of p38 MAPK. Additionally blue LED irradiation of mice injected with CT-26 cells expressing luciferase decreased early stage lung metastasis compared to untreated control mice. These results indicate that blue LED irradiation inhibits cancer cell migration and invasion in vitro and in vivo.
Keyphrases
- light emitting
- cell migration
- induced apoptosis
- computed tomography
- cell cycle arrest
- early stage
- image quality
- contrast enhanced
- small cell lung cancer
- squamous cell carcinoma
- endothelial cells
- magnetic resonance imaging
- cell death
- signaling pathway
- high throughput
- stem cells
- magnetic resonance
- long non coding rna
- small molecule
- oxidative stress
- mesenchymal stem cells
- cell proliferation
- amino acid
- ms ms
- binding protein
- bone marrow
- combination therapy
- hyaluronic acid