Abstract | BACKGROUND/AIM: MATERIALS AND METHODS: The cell viability, cell adhesion, gelatin zymography assay, transwell migration and invasion assay, and western blotting analysis were used to investigate the effects of etomidate on A549 cells. RESULTS: In our study, etomidate showed low cytotoxicity, inhibited cell adhesion, and suppressed the migration and invasion in A549 cells. The activity of matrix metallopeptidase 2 (MMP2) was reduced by 48 h treatment of etomidate. Results of western blotting analysis indicated that etomidate down-regulated the expression of protein kinase C, MMP7, MMP1, MMP9, and p-p-38, but up-regulated that of RAS, phosphoinositide 3-kinase, and phosphor-extracellular-signal related kinase after 24 and 48 h treatment, in A549 cells. CONCLUSION:
Etomidate suppressed the migration and invasion of lung adenocarcinoma A549 cells via inhibiting the expression of MMP1, MMP2, MMP7 and MMP9, and provides potential therapeutic targets for lung cancer treatment.
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Authors | Chin-Nan Chu, King-Chuen Wu, Wai-Shan Chung, Li-Cheng Zheng, Ta-Kuo Juan, Yung-Ting Hsiao, Shu-Fen Peng, Jung-Long Yang, Yi-Shih Ma, Rick Sai-Chuen Wu, Jing-Gung Chung |
Journal | Anticancer research
(Anticancer Res)
Vol. 39
Issue 1
Pg. 215-223
(Jan 2019)
ISSN: 1791-7530 [Electronic] Greece |
PMID | 30591461
(Publication Type: Journal Article)
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Copyright | Copyright© 2019, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved. |
Chemical References |
- Neoplasm Proteins
- Metalloendopeptidases
- Etomidate
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Topics |
- A549 Cells
- Adenocarcinoma of Lung
(drug therapy, genetics, pathology)
- Apoptosis
(drug effects)
- Cell Adhesion
(drug effects)
- Cell Movement
(drug effects)
- Cell Proliferation
(drug effects)
- Etomidate
(pharmacology)
- Gene Expression Regulation, Neoplastic
(drug effects)
- Humans
- Metalloendopeptidases
(genetics)
- Neoplasm Invasiveness
(genetics)
- Neoplasm Proteins
(genetics)
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