Byers Sarah A, Schafer Blanca, Sappal Darshan S, Brown Jeffery, Price David H
Department of Biochemistry, University of Iowa, 3130 MERF, Iowa City, IA 52242, USA.
Mol Cancer Ther. 2005 Aug;4(8):1260-7. doi: 10.1158/1535-7163.MCT-05-0109.
MLN944 is a novel compound currently being codeveloped by Millennium Pharmaceuticals and Xenova Ltd. as a cancer therapeutic and is in a phase I clinical trial for solid tumors. Although MLN944 was originally proposed to function as a topoisomerase I and II inhibitor, more recent data has shown that it is a DNA-intercalating agent that does not inhibit the catalytic activity of topoisomerase I or II. We show here that MLN944 inhibits incorporation of radiolabeled precursors into RNA preferentially over incorporation into DNA and protein in HCT116 and H460 cells. To determine if MLN944 inhibits transcription, a human RNA polymerase II in vitro transcription system was used. MLN944 inhibited initiation when added before or after the formation of preinitiation complexes and inhibited elongation at higher concentrations. The preferential inhibition of initiation differentiates MLN944 from actinomycin D, which more strongly inhibits elongation. Transcription of all RNA polymerases was inhibited in nuclei isolated from HeLa cells treated with low concentrations of MLN944. Our data are consistent with transcription as the target of the potent cytotoxic effects of MLN944.
MLN944是一种新型化合物,目前由千禧制药公司和泽诺瓦有限公司联合开发用作癌症治疗药物,正处于实体瘤的I期临床试验阶段。尽管最初认为MLN944作为拓扑异构酶I和II抑制剂发挥作用,但最近的数据表明它是一种DNA嵌入剂,并不抑制拓扑异构酶I或II的催化活性。我们在此表明,在HCT116和H460细胞中,MLN944优先抑制放射性标记前体掺入RNA,而非掺入DNA和蛋白质。为了确定MLN944是否抑制转录,使用了人RNA聚合酶II体外转录系统。在起始前复合物形成之前或之后添加时,MLN944均抑制起始,并在较高浓度下抑制延伸。对起始的优先抑制使MLN944与放线菌素D区分开来,后者更强烈地抑制延伸。在用低浓度MLN944处理的HeLa细胞分离的细胞核中,所有RNA聚合酶的转录均受到抑制。我们的数据与转录作为MLN944强大细胞毒性作用的靶点一致。