國家衛生研究院 NHRI:Item 3990099045/7200
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    題名: Mefloquine induces cell death in prostate cancer cells and provides a potential novel treatment strategy in vivo
    作者: Yan, KH;Lin, YW;Hsiao, CH;Wen, YC;Lin, KH;Liu, CC;Hsieh, MC;Yao, CJ;Yan, MD;Lai, GM;Chuang, SE;Lee, LM
    貢獻者: National Institute of Cancer Research
    摘要: Mefloquine (MQ) is currently in clinical use as a prophylactic treatment for malaria. Previous studies have shown that MQ induces oxidative stress in vitro. The present study investigated the anticancer effects of MQ treatment in PC3 cells. The cell viability was evaluated using sulphorhodamine-B (SRB) staining, while annexin V and propidium iodide (PI) were used as an assay for cell death. Reactive oxygen species (ROS) formation was detected with 2',7'-dichlorofluorescein-diacetate (DCFH-DA), a sensitive intracellular probe, and the alteration of cellular status was defined by trypan blue staining. The results of the present study indicated that MQ has a high cytotoxicity that causes cell death in PC3 cells. MQ markedly inhibited the PC3 cells through nonapoptotic cell death. MQ also induced significant ROS production. The MQ treatment mediated G1 cell cycle arrest and cyclin D1 accumulation through p21 upregulation in the PC3 cells. Moreover, the use of MQ improved the survival of the treatment group compared with the control group in the experimental mice. The present study indicates that MQ possesses potential therapeutic efficacy for the treatment of prostate cancer (PCa) in vivo. These findings provide insights that may aid the further optimization and application of new and existing therapeutic options.
    日期: 2013-05
    關聯: Oncology Letters. 2013 May;5(5):1567-1571.
    Link to: http://dx.doi.org/10.3892/ol.2013.1259
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=1792-1074&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000318385500025
    Cited Times(Scopus): http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84875716471
    顯示於類別:[莊雙恩] 期刊論文

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