Radiosensitizing effect of diosmetin on radioresistant lung cancer cells via Akt signaling pathway.
Zhijie XuYuanliang YanLingfang XiaoShuang DaiShuangshuang ZengLong QianLin WangXue YangYi XiaoZhicheng GongPublished in: PloS one (2017)
Radiotherapy is a powerful tool in the treatment of cancer that has the advantage of preserving normal tissues. However, tumor radioresistance currently remains a major impediment to effective RT. Thus, exploring effective radiation sensitizers is urgently needed. In this study, we have shown that diosmetin, the aglycone of the lavonoid glycoside from olive leaves, citrus fruits and some medicinal herbs, has a promising effect on radiotherapy sensitization. In our results, DIO could induce G1 phase arrest and thus enhance the radiosensitivity of radioresistant A549/IR lung cancer cells. Furthermore, DIO also restrains the IR-induced DNA damage repair by inhibiting the activated Akt signaling pathway. The combination of Akt inhibition (DIO, LY294002 or MK-2206) and radiation potently blocked A549/IR cancer cell proliferation. In summary, these observations suggest that the natural compound DIO could act as a potential drug for the treatment of radioresistant lung cancer cells.
Keyphrases
- signaling pathway
- cell proliferation
- pi k akt
- dna damage
- papillary thyroid
- epithelial mesenchymal transition
- early stage
- induced apoptosis
- radiation induced
- radiation therapy
- oxidative stress
- squamous cell carcinoma
- squamous cell
- locally advanced
- drug induced
- young adults
- combination therapy
- dna repair
- childhood cancer
- climate change
- smoking cessation
- adverse drug
- electronic health record
- endoplasmic reticulum stress