Dexamethasone modified by gamma-irradiation as a novel anticancer drug in human non-small cell lung cancer.
Eun-Hee LeeChul Hong ParkHyo Jin ChoiRemigius Ambrose KawalaHyoung-Woo BaiByung Yeoup ChungPublished in: PloS one (2018)
Dexamethasone (Dex) is widely used in the management of leukemia and lymphoma. While Dex is commonly used for hematological malignancies, the effects of Dex in solid cancer cells remain controversial. To develop a more effective anticancer drug for solid cancers, Dex was modified by ionizing radiation and the anticancer activity of ionizing-radiation-irradiated Dex (Dex-IR) was investigated in human lung cancer cells. Using the MTT assay, the proliferation of non-small cell lung cancer cells was significantly inhibited after treatment with Dex-IR compared with Dex. Furthermore, Dex-IR induced apoptotic cell death and cell cycle arrest of H1650 human lung cancer cells. The invasiveness of H1650 cells was significantly reduced and the matrix metalloproteinase activity was strongly suppressed. These results indicate that Dex-IR acts as a tumor suppressor by both inducing apoptosis and arresting the cell cycle. Although the structure of Dex-IR remains to be determined, our results suggest it may be useful as a novel anticancer agent for the treatment of solid cancers.
Keyphrases
- cell cycle arrest
- cell death
- cell cycle
- endothelial cells
- pi k akt
- induced pluripotent stem cells
- cell proliferation
- high throughput
- emergency department
- induced apoptosis
- stem cells
- diffuse large b cell lymphoma
- mesenchymal stem cells
- endoplasmic reticulum stress
- young adults
- cell therapy
- atomic force microscopy
- combination therapy