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阿霉素损伤:淋巴瘤细胞在体内的修复

Adriamycin damage: in vivo repair by lymphoma cells.

作者信息

Potmesil M, Levin M, Goldfeder A, Silber R

出版信息

J Natl Cancer Inst. 1981 Dec;67(6):1259-63.

PMID:6947109
Abstract

The in vivo repair of ADR-induced cell damage was investigated in the DBA3 transplantable mouse lymphoma. After a single injection of 5 or 15 mg ADR/kg body weight into DBA/2J mice, the survival fraction of clonogens showed a 2.2- to 4.4-fold decrease at 12 or 18 hours post injection and returned to pretreatment levels within 6 hours. These changes were accompanied by the appearance and disappearance of DNA crosslinks and breaks. Because cell division and/or cell loss could not explain the return of clonogens to pretreatment level, the results strongly suggest repair of ADR damage in tumor cells in situ. Such an efficient repair mechanism, responding to a high toxic dose of ADR, constitutes a therapeutically unfavorable event that may contribute to drug resistance.

摘要

在DBA3可移植性小鼠淋巴瘤模型中研究了阿霉素(ADR)诱导的细胞损伤的体内修复情况。向DBA/2J小鼠单次注射5或15mg ADR/kg体重后,克隆原细胞的存活分数在注射后12或18小时下降了2.2至4.4倍,并在6小时内恢复到预处理水平。这些变化伴随着DNA交联和断裂的出现与消失。由于细胞分裂和/或细胞丢失无法解释克隆原细胞恢复到预处理水平的现象,结果强烈提示肿瘤细胞原位存在ADR损伤修复。这种对高毒性剂量ADR产生反应的高效修复机制是一种治疗上不利的情况,可能导致耐药性。

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