Antitumour Complexes and DNA Interactions and their Tools of Analysis: an Approach to Metalointercalators

被引：11

作者：

Barra, Carolina Valerio ^{[1
]}

Netto, Adelino V. G. ^{[1
]}

机构：

[1] Univ Estadual Paulista, Inst Quim Araraquara, Dept Quim Geral & Inorgan, BR-14800060 Araraquara, SP, Brazil

来源：

REVISTA VIRTUAL DE QUIMICA | 2015年 / 7卷 / 06期

关键词：

Antitumour complexes; DNA interaction; metallointercalators;

D O I：

10.5935/1984-6835.20150118

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

DNA is considered to be one of the major targets of anticancer drugs. Cisplatin and its analogues exert their activity by forming covalent bonds with the DNA base pairs. However, the DNA structure enables its interaction with metal complexes in many different modes and intercalation is often observed. Particularly, metallointercalators stand out as a class of potential antitumour agents that could circumvent problems such cellular resistance since their mechanism of action is different from that of cisplatin. The interaction complex-DNA can be studied by various techniques, including reaction with guanosine, electrophoretic mobility shift assay (EMSA), viscosity measurements, spectrocphotometric titration for determination of K-b, DNA thermal denaturation and fluorescence spectroscopy.

引用

收藏

页码：1998 / 2016

页数：19

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