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阿霉素和柔红霉素的嵌入和诱导链断裂:用人基因组 DNA 进行的研究。

Intercalation and induction of strand breaks by adriamycin and daunomycin: a study with human genomic DNA.

机构信息

School of Biotechnology and Biological Sciences, West Bengal University of Technology, Salt Lake, Kolkata, India.

出版信息

DNA Cell Biol. 2012 Mar;31(3):378-87. doi: 10.1089/dna.2011.1299. Epub 2011 Aug 17.

Abstract

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.

摘要

蒽环类抗癌药物阿霉素(ADR)和柔红霉素(DNM)在治疗多种癌症方面具有显著疗效。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发挥作用,但人们普遍认为与 DNA 的嵌入是其活性所必需的。然而,嵌入作用与导致细胞毒性的细胞过程之间的关系尚未建立。本研究旨在探讨嵌入作用与 DNA 链断裂之间是否存在任何关系。通过吸收和荧光方法观察到 ADR 和 DNM 是人类基因组 DNA 的强嵌入剂,这进一步通过热融解温度升高得到证实。DNM 是两者中更好的嵌入剂,这也可以从圆二色光谱变化中明显看出。DNA 链断裂被认为是遗传毒性的一个指标,通过单细胞凝胶电泳(SCGE;彗星试验)进行检测。ADR 和 DNM 在临床使用剂量下对正常人淋巴细胞产生等效的遗传毒性,尽管与嵌入效率无关,但与活性氧的产生呈正相关。

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