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与亲本系AA8相比,DNA拓扑异构酶I抑制剂喜树碱对CHO突变体EM9染色体损伤诱导的G2敏感性更高。

Higher G2 sensitivity to the induction of chromosomal damage in the CHO mutant EM9 than in its parental line AA8 by camptothecin, an inhibitor of DNA topoisomerase I.

作者信息

Palitti F, Cortés F, Bassi L, Di Chiara D, Fiore M, Pinero J

机构信息

Dipartimento di Agrobiologia e Agrochimica, Università degli Studi della Tuscia, Viterbo, Italy.

出版信息

Mutat Res. 1993 Feb;285(2):281-5. doi: 10.1016/0027-5107(93)90116-w.

Abstract

The induction of chromosomal alterations by camptothecin (CPT), an inhibitor of DNA topoisomerase I, in the G2 stage was studied in a CHO mutant cell line EM9, which has an elevated baseline frequency of SCEs, and in its parental cell line AA8. EM9 cells were found to be more sensitive to CPT than the parental cell line. It is proposed that the effect of camptothecin in this phase of the cell cycle is caused by a 'residual' DNA synthesis which is higher in EM9 than in AA8 cells.

摘要

在一个姐妹染色单体互换(SCE)基线频率升高的中国仓鼠卵巢(CHO)突变细胞系EM9及其亲本细胞系AA8中,研究了DNA拓扑异构酶I抑制剂喜树碱(CPT)在G2期诱导染色体改变的情况。发现EM9细胞比亲本细胞系对CPT更敏感。有人提出,喜树碱在细胞周期这个阶段的作用是由一种“残留”DNA合成引起的,这种合成在EM9细胞中比在AA8细胞中更高。

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