Berger S J, Gupta S, Belfi C A, Gosky D M, Mukhtar H
Department of Medicine, Case Western Reserve University, 10900 Euclid Avenue, Cleveland, OH 44106, USA.
Biochem Biophys Res Commun. 2001 Oct 19;288(1):101-5. doi: 10.1006/bbrc.2001.5736.
DNA topoisomerases I and II are essential for cell survival and play critical roles in DNA metabolism and structure. Inhibitors of topoisomerase constitute a novel family of antitumor agents with demonstrated clinical activity in human malignancies. The clinical use of these agents is limited due to severe toxic effects on normal cells. Therefore, there is a need to develop novel, nontoxic topoisomerase inhibitors that have the ability to spare normal cells. Recent studies have shown that green tea and its major polyphenolic constituent, epigallocatechin-3-gallate (EGCG), impart growth inhibitory responses to cancer cells but not to normal cells. Based on the knowledge that EGCG induces DNA damage, cell cycle arrest, and apoptosis, we considered the possibility of the involvement of topoisomerase in the antiproliferative response of EGCG. Here, for the first time, we show that EGCG inhibits topoisomerase I, but not topoisomerase II in several human colon carcinoma cell lines. Based on this study it is tempting to suggest that combination of EGCG with other conventional topoisomerase inhibitors could be an improved strategy for treatment of colon cancer. The possible role of EGCG as a chemotherapeutic agent needs to be investigated.
DNA拓扑异构酶I和II对细胞存活至关重要,在DNA代谢和结构中发挥关键作用。拓扑异构酶抑制剂构成了一类新型抗肿瘤药物,在人类恶性肿瘤中已显示出临床活性。由于对正常细胞有严重毒性作用,这些药物的临床应用受到限制。因此,需要开发新型、无毒的拓扑异构酶抑制剂,使其能够保护正常细胞。最近的研究表明,绿茶及其主要多酚成分表没食子儿茶素-3-没食子酸酯(EGCG)对癌细胞有生长抑制作用,但对正常细胞没有。基于EGCG可诱导DNA损伤、细胞周期停滞和凋亡这一认识,我们考虑了拓扑异构酶参与EGCG抗增殖反应的可能性。在此,我们首次表明,EGCG在几种人结肠癌细胞系中抑制拓扑异构酶I,但不抑制拓扑异构酶II。基于这项研究,很诱人地提出,EGCG与其他传统拓扑异构酶抑制剂联合使用可能是治疗结肠癌的一种改进策略。EGCG作为化疗药物的潜在作用需要进一步研究。