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Direct evidence of mitochondrial G-quadruplex DNA by using fluorescent anti-cancer agents

机译:使用荧光抗癌剂的线粒体G四联体DNA的直接证据

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摘要

G-quadruplex (G4) is a promising target for anti-cancer treatment. In this paper, we provide the first evidence supporting the presence of G4 in the mitochondrial DNA (mtDNA) of live cells. The molecular engineering of a fluorescent G4 ligand, 3,6-bis(1-methyl-4-vinylpyridinium) carbazole diiodide (BMVC), can change its major cellular localization from the nucleus to the mitochondria in cancer cells, while remaining primarily in the cytoplasm of normal cells. A number of BMVC derivatives with sufficient mitochondrial uptake can induce cancer cell death without damaging normal cells. Fluorescence studies of these anti-cancer agents in live cells and in isolated mitochondria from HeLa cells have demonstrated that their major target is mtDNA. In this study, we use fluorescence lifetime imaging microscopy to verify the existence of mtDNA G4s in live cells. Bioactivity studies indicate that interactions between these anti-cancer agents and mtDNA G4 can suppress mitochondrial gene expression. This work underlines the importance of fluorescence in the monitoring of drug-target interactions in cells and illustrates the emerging development of drugs in which mtDNA G4 is the primary target.
机译:G-四联体(G4)是抗癌治疗的有希望的目标。在本文中,我们提供了第一个支持活细胞线粒体DNA(mtDNA)中存在G4的证据。荧光G4配体3,6-双(1-甲基-4-乙烯基吡啶)咔唑二碘化物(BMVC)的分子工程学可以改变其主要细胞定位,从癌细胞的核到线粒体,而主要保留在癌细胞中。正常细胞的细胞质。许多具有足够线粒体摄取的BMVC衍生物可以诱导癌细胞死亡而不会损害正常细胞。对这些抗癌剂在活细胞和HeLa细胞分离的线粒体中的荧光研究表明,它们的主要靶标是mtDNA。在这项研究中,我们使用荧光寿命成像显微镜来验证活细胞中mtDNA G4s的存在。生物活性研究表明,这些抗癌药与mtDNA G4之间的相互作用可以抑制线粒体基因表达。这项工作强调了荧光在监测细胞中药物-靶标相互作用中的重要性,并阐明了以mtDNA G4为主要靶标的药物的新兴发展。

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