Tewey K M, Rowe T C, Yang L, Halligan B D, Liu L F
Science. 1984 Oct 26;226(4673):466-8. doi: 10.1126/science.6093249.
Adriamycin (doxorubicin), a potent antitumor drug in clinical use, interacts with nucleic acids and cell membranes, but the molecular basis for its antitumor activity is unknown. Similar to a number of intercalative antitumor drugs and nonintercalative epipodophyllotoxins (VP-16 and VM-26), adriamycin has been shown to induce single- and double-strand breaks in DNA. These strand breaks are unusual because a covalently bound protein appears to be associated with each broken phosphodiester bond. In studies in vitro, mammalian DNA topoisomerase II mediates DNA damage by adriamycin and other related antitumor drugs.
阿霉素(多柔比星)是一种临床使用的强效抗肿瘤药物,它与核酸和细胞膜相互作用,但其抗肿瘤活性的分子基础尚不清楚。与许多嵌入性抗肿瘤药物和非嵌入性鬼臼毒素(依托泊苷和替尼泊苷)类似,阿霉素已被证明可诱导DNA单链和双链断裂。这些链断裂很不寻常,因为每个断裂的磷酸二酯键似乎都与一种共价结合的蛋白质相关。在体外研究中,哺乳动物DNA拓扑异构酶II介导阿霉素和其他相关抗肿瘤药物对DNA的损伤。