Sheng Y, Pero R W, Amiri A, Bryngelsson C
Department of Cell and Molecular Biology, University of Lund, Sweden.
Anticancer Res. 1998 Sep-Oct;18(5A):3363-8.
Growth inhibitory activities of novel water extracts of Uncaria tomentosa (C-Med-100) were examined in vitro using two human leukemic cell lines (K562 and HL60) and one human EBV-transformed B lymphoma cell line (Raji). The proliferative capacities of HL60 and Raji cells were strongly suppressed in the presence of the C-Med-100 while K562 was more resistant to the inhibition. Furthermore, the antiproliferative effect was confirmed using the clonogenic assay, which showed a very close correlation between C-Med-100 concentration and the surviving fraction. The suppressive effect of Uncaria tomentosa extracts on tumor cell growth appears to be mediated through induction of apoptosis which was demonstrated by characteristic morphological changes, internucleosomal DNA fragmentation after agarose gel electrophoresis and DNA fragmentation quantification. C-Med-100 induced a delayed type of apoptosis becoming most dose-dependently prominent after 48 hours of exposure. Both DNA single and double strand breaks were increased 24 hours after C-Med-100 treatment, which suggested a well-established linkage between the DNA damage and apoptosis. The induction of DNA strand breaks coupled to apoptosis may explain the growth inhibition of the tumor cells by Uncaria tomentosa extracts. These results provide the first direct evidence for the antitumor properties of Uncaria tomentosa extracts to be via a mechanism of selective induction of apoptosis.
使用两种人类白血病细胞系(K562和HL60)和一种人类EB病毒转化的B淋巴瘤细胞系(Raji),在体外检测了钩藤(C-Med-100)新型水提取物的生长抑制活性。在存在C-Med-100的情况下,HL60和Raji细胞的增殖能力受到强烈抑制,而K562对这种抑制更具抗性。此外,通过克隆形成试验证实了抗增殖作用,该试验表明C-Med-100浓度与存活分数之间存在非常密切的相关性。钩藤提取物对肿瘤细胞生长的抑制作用似乎是通过诱导凋亡介导的,这通过特征性形态变化、琼脂糖凝胶电泳后核小体间DNA片段化和DNA片段化定量得以证明。C-Med-100诱导了一种延迟型凋亡,在暴露48小时后最呈剂量依赖性显著。在C-Med-100处理24小时后,DNA单链和双链断裂均增加,这表明DNA损伤与凋亡之间存在明确的联系。与凋亡相关的DNA链断裂的诱导可能解释了钩藤提取物对肿瘤细胞的生长抑制作用。这些结果为钩藤提取物的抗肿瘤特性是通过选择性诱导凋亡机制提供了首个直接证据。