Dziegielewska Barbara, Kowalski David, Beerman Terry A
Department of Pharmacology and Therapeutics, Roswell Park Cancer Institute, Elm and Carlton Streets, Buffalo, New York 14263, USA.
Biochemistry. 2004 Nov 9;43(44):14228-37. doi: 10.1021/bi049407x.
Ecteinascidin 743 (Et743) is a highly cytotoxic anticancer agent isolated from the squirt Ecteinascidia turbinate, which alkylates DNA in the minor groove at GC-rich sequences resulting in an unusual bending toward the major groove. The ability of Et743 to block DNA replication was studied using the well-established simian virus (SV40) model for mammalian DNA replication in cells and cell-free extracts. Intracellular SV40 DNA isolated from Et743-treated BSC-1 cells was analyzed by native, two-dimensional agarose gel electrophoresis. A low frequency of Et743 adducts detected at 30-100 nM drug concentrations inhibited SV40 origin activity and induced formation of unusual DNA replication intermediates. Under cell-free conditions, only a high Et743 adduct frequency reduced SV40 DNA synthesis. Comparative studies involving related DNA alkylators, tomamycin and saframycin A, revealed inhibition of SV40 DNA replication in cells at concentrations approximately 10 times higher than Et743. Under cell-free conditions tomamycin- or saframycin-A-adducted DNA templates inhibited DNA synthesis similarly to Et743. Et743 appears to be unusual among other alkylators, because its adducts strongly inhibit intracellular SV40 DNA replication but are relatively weak as cis inhibitors as measured under cell-free conditions.
埃博霉素743(Et743)是一种从被囊动物海鞘中分离出的具有高度细胞毒性的抗癌药物,它能使富含GC序列的DNA小沟中的DNA发生烷基化,导致DNA向大沟方向发生异常弯曲。利用成熟的猿猴病毒(SV40)模型,在细胞和无细胞提取物中研究了Et743阻断DNA复制的能力。通过天然的二维琼脂糖凝胶电泳分析从经Et743处理的BSC-1细胞中分离出的细胞内SV40 DNA。在30 - 100 nM药物浓度下检测到的低频Et743加合物抑制了SV40的起始活性,并诱导形成异常的DNA复制中间体。在无细胞条件下,只有高频率的Et743加合物会降低SV40 DNA的合成。涉及相关DNA烷基化剂托马霉素和沙弗霉素A的比较研究表明,在细胞中抑制SV40 DNA复制的浓度比Et743高约10倍。在无细胞条件下,托马霉素或沙弗霉素A加合的DNA模板对DNA合成的抑制作用与Et743类似。Et743在其他烷基化剂中似乎很特别,因为其加合物强烈抑制细胞内SV40 DNA复制,但在无细胞条件下作为顺式抑制剂相对较弱。