Department of Pharmaceutical Sciences, Lipscomb University College of Pharmacy, Nashville, Tennessee 37204-3951, USA.
Biochemistry. 2011 Jun 28;50(25):5660-7. doi: 10.1021/bi200438m. Epub 2011 Jun 2.
Etoposide is a topoisomerase II poison that is used to treat a variety of human cancers. Unfortunately, 2-3% of patients treated with etoposide develop treatment-related leukemias characterized by 11q23 chromosomal rearrangements. The molecular basis for etoposide-induced leukemogenesis is not understood but is associated with enzyme-mediated DNA cleavage. Etoposide is metabolized by CYP3A4 to etoposide catechol, which can be further oxidized to etoposide quinone. A CYP3A4 variant is associated with a lower risk of etoposide-related leukemias, suggesting that etoposide metabolites may be involved in leukemogenesis. Although etoposide acts at the enzyme-DNA interface, several quinones poison topoisomerase II via redox-dependent protein adduction. The effects of etoposide quinone on topoisomerase IIα-mediated DNA cleavage have been examined previously. Although findings suggest that the activity of the quinone is slightly greater than that of etoposide, these studies were carried out in the presence of significant levels of reducing agents (which should reduce etoposide quinone to the catechol). Therefore, we examined the ability of etoposide quinone to poison human topoisomerase IIα in the absence of reducing agents. Under these conditions, etoposide quinone was ∼5-fold more active than etoposide at inducing enzyme-mediated DNA cleavage. Consistent with other redox-dependent poisons, etoposide quinone inactivated topoisomerase IIα when incubated with the protein prior to DNA and lost activity in the presence of dithiothreitol. Unlike etoposide, the quinone metabolite did not require ATP for maximal activity and induced a high ratio of double-stranded DNA breaks. Our results support the hypothesis that etoposide quinone contributes to etoposide-related leukemogenesis.
依托泊苷是一种拓扑异构酶 II 抑制剂,用于治疗多种人类癌症。不幸的是,2-3%接受依托泊苷治疗的患者会出现以 11q23 染色体重排为特征的治疗相关白血病。依托泊苷诱导白血病发生的分子基础尚不清楚,但与酶介导的 DNA 断裂有关。依托泊苷被 CYP3A4 代谢为依托泊苷儿茶酚,后者可进一步氧化为依托泊苷醌。CYP3A4 的一种变体与较低的依托泊苷相关白血病风险相关,表明依托泊苷代谢物可能参与白血病的发生。尽管依托泊苷作用于酶-DNA 界面,但几种醌类通过氧化还原依赖的蛋白质加合使拓扑异构酶 II 中毒。先前已经研究了依托泊苷醌对拓扑异构酶 IIα 介导的 DNA 断裂的影响。尽管研究结果表明醌的活性略高于依托泊苷,但这些研究是在存在大量还原剂的情况下进行的(还原剂应将依托泊苷醌还原为儿茶酚)。因此,我们在没有还原剂的情况下检查了依托泊苷醌使人类拓扑异构酶 IIα中毒的能力。在这些条件下,依托泊苷醌诱导酶介导的 DNA 断裂的活性比依托泊苷高约 5 倍。与其他氧化还原依赖的毒物一致,依托泊苷醌在与蛋白质孵育之前与拓扑异构酶 IIα 失活,在存在二硫苏糖醇的情况下失去活性。与依托泊苷不同,醌类代谢物不需要 ATP 即可达到最大活性,并诱导双链 DNA 断裂的高比值。我们的结果支持这样的假设,即依托泊苷醌有助于依托泊苷相关的白血病发生。