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蒽环类药物诱导的链间DNA交联与其生物学活性的相关性。

Relevance of interstrand DNA crosslinking induced by anthracyclines for their biological activity.

作者信息

Skladanowski A, Konopa J

机构信息

Department of Pharmaceutical Technology and Biochemistry, Technical University of Gdańsk, Poland.

出版信息

Biochem Pharmacol. 1994 Jun 15;47(12):2279-87. doi: 10.1016/0006-2952(94)90266-6.

Abstract

The relevance of interstrand DNA crosslinking induced by anthracyclines for their cytotoxic action was studied in several biological systems with cells differing in sensitivity towards these compounds. It was done by establishing the correlation between DNA crosslinking and cytotoxic activity of anthracyclines. The study showed that there is a strong positive correlation between cytotoxic activity of anthracyclines and their DNA crosslinking potency in HeLa S3 cells for a group of six Daunomycin derivatives (r = 0.97) as well as for all the studied 13 anthracyclines of divergent chemical structure (r = 0.95). Similar relationships between cytotoxic activity and DNA crosslinking ability was found for Adriamycin and Daunomycin in three other cellular systems: (i) in LoVo and about 20-fold Adriamycin-resistant LoVo/DX human colon adenocarcinoma cells, (ii) CHO-K1 and its Adriamycin-hypersensitive mutant CHO-ADR5 Chinese hamster ovary cells and (iii) HeLa S3 cells sensitized about 3-fold to cytotoxic action of Adriamycin and Daunomycin by lowering intracellular glutathione content, to about 10% of normal level, by buthionine sulfoximine treatment. The presented results show that DNA crosslinking induced by anthracyclines may be responsible for the cytotoxic activity of these compounds.

摘要

在几个对这些化合物敏感性不同的细胞生物系统中,研究了蒽环类药物诱导的链间DNA交联与其细胞毒性作用的相关性。这是通过建立DNA交联与蒽环类药物细胞毒性活性之间的相关性来完成的。研究表明,对于一组六种柔红霉素衍生物(r = 0.97)以及所有研究的13种化学结构不同的蒽环类药物(r = 0.95),在HeLa S3细胞中,蒽环类药物的细胞毒性活性与其DNA交联能力之间存在很强的正相关。在其他三个细胞系统中,阿霉素和柔红霉素也发现了细胞毒性活性与DNA交联能力之间的类似关系:(i)在LoVo和对阿霉素耐药约20倍的LoVo/DX人结肠腺癌细胞中;(ii)在CHO-K1及其对阿霉素敏感的突变体CHO-ADR5中国仓鼠卵巢细胞中;(iii)通过丁硫氨酸亚砜胺处理将细胞内谷胱甘肽含量降低至正常水平的约10%,从而使HeLa S3细胞对阿霉素和柔红霉素的细胞毒性作用敏感约3倍。所呈现的结果表明,蒽环类药物诱导的DNA交联可能是这些化合物细胞毒性活性的原因。

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