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首页> 外文期刊>DNA and Cell Biology >Intercalation and induction of strand breaks by adriamycin and daunomycin: a study with human genomic DNA.
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Intercalation and induction of strand breaks by adriamycin and daunomycin: a study with human genomic DNA.

机译:阿霉素和道诺霉素的插入和链断裂的诱导:一项人类基因组DNA研究。

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摘要

The anticancer drugs Adriamycin (ADR) and Daunomycin (DNM) of the anthracycline family are effective in treating a variety of cancers. Although their interactions with other cellular targets may play a role in the selective cytotoxicity of these drugs, it is generally believed that intercalation with DNA is essential for their activity. However, a relationship has not yet been established between intercalation and cellular processes leading to cytotoxicity. The present study was designed to investigate the relationship, if any, between intercalation and DNA strand breaks. ADR and DNM were observed to be strong intercalators of human genomic DNA by absorption and fluorimetric methods that were further substantiated by rise in thermal melting temperature. DNM is the better intercalator of the two, which is also evident from circular dichroic spectral changes. DNA strand breaks, considered to be an index of genotoxicity, was assayed by single cell gel electrophoresis (SCGE; comet assay). ADR and DNM induced equivalent genotoxicity in normal human lymphocytes at a clinically used dose, which was observed to be independent of intercalation efficiency though positively correlated to yield of reactive oxygen species.
机译:蒽环类的抗癌药阿霉素(ADR)和道诺霉素(DNM)可有效治疗多种癌症。尽管它们与其他细胞靶标的相互作用可能在这些药物的选择性细胞毒性中起作用,但通常认为与DNA的插入对其活性至关重要。但是,在插入和导致细胞毒性的细胞过程之间尚未建立关系。本研究旨在调查嵌入和DNA链断裂之间的关系(如果有)。通过吸收和荧光法观察到ADR和DNM是人类基因组DNA的强插入物,其通过热解链温度的升高进一步证实。 DNM是两者中较好的嵌入剂,这也可以从圆二色性光谱变化中看出。通过单细胞凝胶电泳(SCGE;彗星试验)测定被认为是遗传毒性指标的DNA链断裂。在临床使用剂量下,ADR和DNM在正常人淋巴细胞中诱导了同等的遗传毒性,尽管与活性氧的产量呈正相关,但观察到它与插层效率无关。

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