Ishino A, Kusama K, Watanabe S, Sakagami H
Department of Dental Pharmacology, Meikai University School of Dentistry, Saitama, Japan.
Anticancer Res. 1999 Nov-Dec;19(6B):5197-201.
Epigallocatechin gallate (EGCG) induced apoptotic cell death in two human oral tumor cell lines (HSC-2, HSG), as judged by TUNEL method which detects DNA nick. Furthermore, the cytoplasm of EGCG-treated HSG cells was stained by M30 monoclonal antibody, which detects the degradation product of cytokeratin by activated caspase. The apoptosis-inducing activity of EGCG was significantly reduced by millimolar concentrations of CoCl2. CoCl2 also inhibited the cytotoxic activity of sodium ascorbate, gallic acid and curcumin, but not that of sodium-5, 6-benzylidene-L-ascorbate (SBA). This suggests that SBA, an antitumor agent, induces cell death by a different mechanism from that of other antioxidants used in this study. The possible role of CoCl2 for cell survival was discussed.
通过检测DNA切口的TUNEL法判断,表没食子儿茶素没食子酸酯(EGCG)可诱导两种人类口腔肿瘤细胞系(HSC-2、HSG)发生凋亡性细胞死亡。此外,用检测活化半胱天冬酶切割细胞角蛋白产生的降解产物的M30单克隆抗体对经EGCG处理的HSG细胞的细胞质进行染色。毫摩尔浓度的CoCl2可显著降低EGCG的凋亡诱导活性。CoCl2还抑制了抗坏血酸钠、没食子酸和姜黄素的细胞毒活性,但不抑制5,6-亚苄基-L-抗坏血酸钠(SBA)的细胞毒活性。这表明,作为一种抗肿瘤剂,SBA通过与本研究中使用的其他抗氧化剂不同的机制诱导细胞死亡。文中讨论了CoCl2对细胞存活的可能作用。