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RNAm expression profile of cancer marker genes in HepG2 cells treated with different concentrations of a new indolin-3-one from Pseudomonas aeruginosa

机译:不同浓度铜绿假单胞菌新吲哚-3-酮处理后的HepG2细胞中癌标志物基因的RNAm表达谱

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摘要

The present study tested the effects of a newly identified indolin-3-one compound (compound >1), produced by Pseudomonas aeruginosa, on HepG2 cells. The MTT assays demonstrated decreased metabolic activities in HepG2 cells treated with compound >1, with dose- and time-dependent intensifying effect, starting at a concentration of 40 µM. The IC50 after 24, 48, 72, and 96 h treatments were 41.35, 52.7, 92.79 and 66.65 μM of compound >1, respectively. Below 80 µM, no significative damage on erythrocytes membranes was observed by the hemolytic assays. The RT-qPCR revealed that the compound modulated key genes involved in carcinogenesis process, indicating possible indolin-3-one mechanisms of action. The data showed that gene expression alterations promoted by compound >1, in concentrations up to 60 μM after 48 h, led to a decrease in cellular progression and there was no direct cellular damage. In addition, non-cytotoxic concentrations of compound >1 halved the concentration of the chemotherapeutic doxorubicin, maintaining similar therapeutic effect against HepG2 cells. The novelty of the molecule and the biological activities observed in the present study emphasize the potential of the compound >1 in cancer therapy research.
机译:本研究测试了由铜绿假单胞菌产生的一种新鉴定的吲哚-3-酮化合物(化合物> 1 )对HepG2细胞的作用。 MTT分析表明,化合物> 1 处理后的HepG2细胞代谢活性降低,剂量和时间依赖性增强作用,起始浓度为40μmM。 24、48、72和96 h处理后的IC50分别为化合物> 1 的41.35、52.7、92.79和66.65μM。在80μm以下,通过溶血分析未观察到对红细胞膜的显着损害。 RT-qPCR显示该化合物调节了致癌过程中涉及的关键基因,表明可能是吲哚3的一个作用机理。数据表明,化合物> 1 促进的基因表达改变在浓度达48 afterh后高达60μM,导致细胞进程减少,并且没有直接的细胞损伤。此外,化合物> 1 的非细胞毒性浓度使化疗药物阿霉素的浓度减半,从而保持了对HepG2细胞的相似治疗效果。本研究中观察到的分子的新颖性和生物学活性强调了化合物> 1 在癌症治疗研究中的潜力。

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