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青蒿琥酯具有抗白血病特性,三氧化二砷可增强其抗白血病特性。

Artesunate possesses anti-leukemia properties that can be enhanced by arsenic trioxide.

作者信息

Li Ying, Feng Lili, Li Ying, Jiang Wen, Shan Ningning, Wang Xin

机构信息

Department of Hematology, Provincial Hospital Affiliated to Shandong University , Jinan , P. R. China.

出版信息

Leuk Lymphoma. 2014 Jun;55(6):1366-72. doi: 10.3109/10428194.2013.829573. Epub 2013 Sep 9.

Abstract

Artesunate (ART), an effective and safe anti-malaria drug, also exhibits anticancer activity. We studied the effects of ART on proliferation and apoptosis of human K562 and U937 leukemia cell lines. MTT [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] assay demonstrated that ART inhibits cell growth in a dose- and time-dependent manner. Based on the findings obtained from light, fluorescence and transmission electron microscopy and propidium iodide staining, the effect of ART was shown to be mediated through apoptosis. In parallel, ART treatment increased Fas expression, while it decreased the c-Fos level in K562 cells. Furthermore, co-treatment with arsenic trioxide (ATO) significantly facilitated ART-induced K562 cell apoptosis. These findings demonstrated that ART had an antitumor activity against K562 and U937 leukemia cells, largely due to inhibition of proliferation and induction of apoptosis via the intrinsic pathway; and this tumoricidal function could be enhanced by ATO.

摘要

青蒿琥酯(ART)是一种有效且安全的抗疟疾药物,也具有抗癌活性。我们研究了ART对人K562和U937白血病细胞系增殖和凋亡的影响。MTT [3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐] 实验表明,ART以剂量和时间依赖性方式抑制细胞生长。基于光学、荧光和透射电子显微镜以及碘化丙啶染色的结果,显示ART的作用是通过凋亡介导的。同时,ART处理增加了Fas表达,而降低了K562细胞中的c-Fos水平。此外,与三氧化二砷(ATO)联合处理显著促进了ART诱导的K562细胞凋亡。这些发现表明,ART对K562和U937白血病细胞具有抗肿瘤活性,主要是由于通过内源性途径抑制增殖和诱导凋亡;并且ATO可以增强这种杀瘤功能。

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