中山醫學大學機構典藏 CSMUIR:Item 310902500/11463
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    题名: The in vitro and in vivo apoptotic effects of Mahonia oiwakensis on human lung cancer cells.
    作者: Wong, BS
    Hsiao, YC
    Lin, TW
    Chen, KS
    Chen, PN
    Kuo, WH
    Chu, SC
    Hsieh, YS
    贡献者: 中山醫學大學
    关键词: Mahonia;NSCLC;Chemoprevention;Apoptosis
    日期: 2009
    上传时间: 2015-07-21T07:51:53Z (UTC)
    ISSN: 0009-2797
    摘要: Both the root and stem bark of Mahonia species were popular folk medicines. The plant has several proven biological activities including anti-bacterial, anti-fungal, and anti-inflammatory effects. However, Mahonia has not been studied for its anticancer effects. In the present study, we made extracts from Mahonia oiwakensis (MOE), a selected species in Taiwan, and investigated their effects on various human lung cells. We found that MOE-induced apoptotic death in human A549 non-small-cell lung carcinoma (NSCLC) cells in a dose- and time-dependent manner. Treatment with the extracts also caused an increase in the sub-G1 fraction of cells, chromosome condensation, and DNA fragmentation. The mitochondrial-mediated pathway was implicated in this MOE-induced apoptosis as evidenced by the activation of the caspase cascade, cleavage of poly (ADP-ribose) polymerase (PARP), disruption of mitochondrial membrane potential, and release of cytochrome C. A higher ratio of Bax/Bcl-2 proteins and cleavage of Bid were also observed in MOE-induced cell apoptosis. In A549 tumor-xenografted nude mice, MOE also retarded in vivo proliferation (P<0.05) and induced apoptosis in tumor cells, as shown by a decrease in Ki-67-positive staining (P<0.05) and increased transferase-mediated dUTP nick-end labeling (TUNEL)-positive staining (P<0.05). In conclusion, MOE inhibits the growth of human lung cancer cells in vitro and in vivo, suggesting that it may have therapeutic potential against human lung cancer.
    URI: https://ir.csmu.edu.tw:8080/ir/handle/310902500/11463
    http://dx.doi.org/10.1016/j.cbi.2009.02.011
    關聯: Chem Biol Interact. 2009 Jul 15;180(2):165-74.
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