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A platinum blue complex exerts its cytotoxic activity via DNA damage and induces apoptosis in cancer cells

机译:铂蓝色复合物通过DNA损伤发挥其细胞毒性活性,并在癌细胞中诱导细胞凋亡

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摘要

Here, we describe the characteristics of a Pt-blue complex [Pt-4(2-atp)(8)(H2O)(OH)] (2-atp: 2-aminothiophenol) as a prodrug for its DNA-binding properties and its use in cancer therapy. The nature of the interaction between the Pt-blue complex and DNA was evaluated based on spectroscopic measurements, the electronic absorption spectra, thermal behavior, viscosity, fluorometric titration, and agarose gel electrophoresis. Our results suggested that the compound was able to partially intercalate DNA and appeared to induce both single- and double-stranded breaks (DBS) on DNA in vitro, but no DSBs in cells. The ability of the compound to induce DNA damage was dependent on reactive oxygen species (ROS) in vitro. There was also elevated formation of ROS and SOD expression in response to drug treatment in cell culture. The complex was found to be more cytotoxic to cancer cells in comparison with noncancer controls using WST-1 assay. The mean of cell death was determined to be apoptosis as assessed via biochemical, morphological, and molecular observations, including DNA condensation/fragmentation analysis, live cell imaging microscopy, TUNEL analyses, and increase in the levels of pro-apoptotic genes such as Bag3, Bak, Bik, Bmf, and Hrk. Hence, the Pt-blue complex under study grants premise for further studies.
机译:在此,我们描述了Pt-Blue络合物[Pt-4(2-ATP)(8)(H2O)(OH)](2-ATP:2-氨基噻吩苯酚)作为其DNA结合性能的前药的特性和它在癌症治疗中的用途。基于光谱测量,电子吸收光谱,热行为,粘度,荧光滴定和琼脂糖凝胶电泳评估Pt-Blue复合物和DNA之间的相互作用性质。我们的结果表明该化合物能够部分地插入DNA,并且似乎在体外诱导单链和双链突破(DBS),但细胞中没有DSB。化合物诱导DNA损伤的能力依赖于体外反应性氧物质(ROS)。响应于细胞培养的药物治疗,还升高了ROS和SOD表达的形成。与使用WST-1测定的非癌症对照相比,发现该复合物对癌细胞更具细胞毒性。确定细胞死亡的平均值是通过生物化学,形态学和分子观察评估的细胞凋亡,包括DNA缩合/碎片分析,活细胞成像显微镜,TUNEL分析和增加促群凋亡基因,如BAG3, Bak,Bik,BMF和HRK。因此,PT-Blue复合体正在研究授予进一步研究的前提。

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