Calotropis gigantea extract induces apoptosis through extrinsic/intrinsic pathways and reactive oxygen species generation in A549 and NCI-H1299 non-small cell lung cancer cells
文献类型: 外文期刊
第一作者: Lee, Jiyon
作者: Lee, Jiyon;Jang, Hui-Ju;Chun, Hyunwoo;Pham, Thu-Huyen;Bak, Yesol;Shin, Jong-Woon;Jin, Hang;Yoon, Do-Young;Jin, Hang;Kim, Yong-In;Ryu, Hyung Won;Oh, Sei Ryang;Yoon, Do-Young
作者机构:
关键词: Calotropis gigantea; Non-small cell lung cancer cell; Anti-cancer; Apoptosis; ROS
期刊名称:BMC COMPLEMENTARY AND ALTERNATIVE MEDICINE ( 影响因子:3.659; 五年影响因子:3.767 )
ISSN: 1472-6882
年卷期: 2019 年 19 卷
页码:
收录情况: SCI
摘要: BackgroundCalotropis gigantea (CG) is a tall and waxy flower that is used as a traditional remedy for fever, indigestion, rheumatism, leprosy, and leukoderma. However, the precise mechanisms of its anticancer effects have not yet been examined in human non-small cell lung cancer (NSCLC) cells. In this study, we investigated whether CG extract exerted an apoptotic effect in A549 and NCI-H1299 NSCLC cells.MethodsThe ethanol extract of CG was prepared, and its apoptotic effects on A549 and NCI-H1299 NSCLC cells were assessed by using the 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxy methoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium (MTS) assay, annexin V-fluorescein isothiocyanate/propidium iodide (PI) staining, cell cycle analysis, real-time polymerase chain reaction (RT-PCR), western blotting, JC-1 staining, and ROS detection assay.ResultsThe CG extract induced apoptosis through the stimulation of intrinsic and extrinsic signaling pathways in A549 and NCI-H1299 lung cancer cells. Cell cycle arrest was induced by the CG extract in both cell lines. Reactive oxygen species (ROS), which can induce cell death, were also generated in the CG-treated A549 and NCI-H1299 cells.ConclusionsThese data confirmed that CG caused apoptosis through the activation of extrinsic and intrinsic pathways, cell cycle arrest, and ROS generation in A549 and NCI-H1299 lung cancer cells. Thus, CG can be suggested as a potential agent for lung cancer therapy.
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