首页> 外文期刊>Expert opinion on therapeutic targets >Antiproliferative effects of a new α-lipoic acid derivative, DHL-HisZnNa, in HT29 human colon cancer cells in vitro.
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Antiproliferative effects of a new α-lipoic acid derivative, DHL-HisZnNa, in HT29 human colon cancer cells in vitro.

机译:新的α-硫辛酸衍生物DHL-HisZnNa在HT29人结肠癌细胞中的抗增殖作用。

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α-Lipoic acid has been reported to induce apoptosis in several cancer cell lines. However, it is prone to oxidation, polymerization and desulfurization, and is insoluble in water. In this study an α-lipoic acid derivative, sodium N-(dihydrolipoyl)-l-histidinate zinc complex (DHL-HisZnNa), was synthesized, which can eliminate active oxygen species. The antiproliferative effects of DHL-HisZnNa, on human colon cancer cell HT29 in vitro, were evaluated.Whether DHL-HisZnNa elicits its antiproliferative effects by inducing apoptosis and cell cycle arrest, was investigated. Expressions of cell-cycle-related proteins and their phosphorylation on HT-29 was also analyzed.DHL-HisZnNa inhibited cancer cell growth in cultures. Cell cycle analysis by flow cytometry showed time-dependent accumulation of HT-29 cells in G1 phase after exposure to DHL-HisZnNa. Analysis of DNA fragmentation did not reveal evidence of apoptosis after exposure to DHL-HisZnNa. Cells treated with DHL-HisZnNa showed an increase in p53 phosphorylation with the Bio-Plex Phosphoprotein assay. DHL-HisZnNa increased protein levels of the cyclin-dependent kinase inhibitor p21 and decreased that of phosphorylated retinoblastoma protein (Rb) by western blot analysis. Results obtained with DHL-HisZnNa are on a single colon cancer cell line and not comparative experiments with α-lipoic acid.This is the first study, to our knowledge, to report the antiproliferative effects of DHL-HisZnNa and the molecular mechanisms by which it inhibits growth of HT29.
机译:据报道,α-硫辛酸可在几种癌细胞系中诱导凋亡。但是,它易于氧化,聚合和脱硫,并且不溶于水。在这项研究中,合成了α-硫辛酸衍生物N-(二氢硫酰基)-1-组氨酸钠锌复合物(DHL-HisZnNa),它可以消除活性氧。研究了DHL-HisZnNa对人结肠癌细胞HT29的体外抗增殖作用。还分析了细胞周期相关蛋白的表达及其在HT-29上的磷酸化。DHL-HisZnNa抑制培养物中癌细胞的生长。通过流式细胞仪进行的细胞周期分析显示,在暴露于DHL-HisZnNa后,G1期的HT-29细胞具有时间依赖性。 DNA片段分析未显示出暴露于DHL-HisZnNa后的凋亡迹象。用Bio-Plex磷酸蛋白测定法,用DHL-HisZnNa处理的细胞显示p53磷酸化增加。通过蛋白质印迹分析,DHL-HisZnNa可增加细胞周期蛋白依赖性激酶抑制剂p21的蛋白水平,并降低磷酸化视网膜母细胞瘤蛋白(Rb)的蛋白水平。 DHL-HisZnNa的结果是在单个结肠癌细胞系上进行的,而不是与α-硫辛酸的对比实验。据我们所知,这是第一个报道DHL-HisZnNa的抗增殖作用及其分子机制的研究。抑制HT29的生长。

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