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8-甲氧基咖啡因诱导分离的L1210细胞核中与蛋白质相关的DNA断裂。

8-methoxycaffeine-induced protein-associated DNA breaks in isolated L1210 cell nuclei.

作者信息

Zignaigo G, Vigani A, Billi G, Brega I, Piccini D, Poggi L, Parodi S, Russo P

机构信息

Istituto Nazionale per la Ricerca sul Cancro, Sezione di Genova.

出版信息

Boll Soc Ital Biol Sper. 1990 Jun;66(6):587-94.

PMID:2175203
Abstract

8-methoxycaffeine (8-MOC) is a caffeine derivative more potent than its parental compound in inducing chromosomal aberrations. 8-MOC has been postulated to produce chromosomal aberrations by DNA topoisomerase II inhibition. The effect of 8-MOC on nuclear DNA were studied by alkaline elution experiments and compared with those of Ellipticine and Adriamycin (ADR). Like Ellipticine and ADR, 8-MOC induced single strand breaks (SSBs), double strand breaks (DSBs), and DNA-protein cross-links (DPCs) in a bell-shaped manner with respect to drug concentration. As in the case of ADR and Ellipticine, 8-MOC induced equal SSB and DPC frequencies. These results could suggest that 8-MOC induces DNA breaks by interacting with DNA topoisomerase II or with a similar DNA metabolism enzyme.

摘要

8-甲氧基咖啡因(8-MOC)是一种咖啡因衍生物,在诱导染色体畸变方面比其母体化合物更具效力。据推测,8-MOC通过抑制DNA拓扑异构酶II产生染色体畸变。通过碱性洗脱实验研究了8-MOC对核DNA的影响,并与椭圆玫瑰树碱和阿霉素(ADR)的影响进行了比较。与椭圆玫瑰树碱和ADR一样,8-MOC以钟形方式诱导单链断裂(SSB)、双链断裂(DSB)和DNA-蛋白质交联(DPC),与药物浓度有关。与ADR和椭圆玫瑰树碱的情况一样,8-MOC诱导的SSB和DPC频率相等。这些结果可能表明,8-MOC通过与DNA拓扑异构酶II或类似的DNA代谢酶相互作用诱导DNA断裂。

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