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首页> 外文期刊>Lipids in Health Disease >Combination of unsaturated fatty acids and ionizing radiation on human glioma cells: cellular, biochemical and gene expression analysis
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Combination of unsaturated fatty acids and ionizing radiation on human glioma cells: cellular, biochemical and gene expression analysis

机译:人胶质瘤细胞中不饱和脂肪酸与电离辐射的结合:细胞,生化和基因表达分析

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Background Based on previous observations a potential resort in the therapy of the particularly radioresistant glioma would be its treatment with unsaturated fatty acids (UFAs) combined with irradiation. Methods We evaluated the effect of different UFAs (arachidonic acid (AA), docosahexaenoic acid (DHA), gamma-linolenic acid (GLA), eicosapentaenoic acid (EPA) and oleic acid (OA)) on human U87 MG glioma cell line by classical biochemical end-point assays, impedance-based, real-time cellular and holographic microscopic analysis. We further analyzed AA, DHA, and GLA at morphological, gene and miRNA expression level. Results Corresponding to LDH-, MTS assays and real-time cytoxicity profiles AA, DHA, and GLA enhanced the radio sensitivity of glioma cells. The collective application of polyunsaturated fatty acids (PUFAs) and irradiation significantly changed the expression of EGR1, TNF-α, NOTCH1, c-MYC, TP53, HMOX1, AKR1C1, NQO1, while up-regulation of GADD45A, EGR1, GRP78, DDIT3, c-MYC, FOSL1 were recorded both in response to PUFA treatment or irradiation alone. Among the analyzed miRNAs miR-146 and miR-181a were induced by DHA treatment. Overexpression of miR-146 was also detected by combined treatment of GLA and irradiation. Conclusions Because PUFAs increased the radio responsiveness of glioma cells as assessed by biochemical and cellular assays, they might increase the therapeutic efficacy of radiation in treatment of gliomas. We demonstrated that treatment with DHA, AA and GLA as adjunct to irradiation up-regulated the expression of oxidative-stress and endoplasmic reticulum stress related genes, and affected NOTCH1 expression, which could explain their additive effects.
机译:背景技术基于先前的观察,在特别耐辐射的神经胶质瘤的治疗中,潜在的手段将是用不饱和脂肪酸(UFA)结合放射治疗。方法我们通过经典方法评估了不同的UFA(花生四烯酸(AA),二十二碳六烯酸(DHA),γ-亚麻酸(GLA),二十碳五烯酸(EPA)和油酸(OA))对人U87 MG胶质瘤细胞系的影响生化终点分析,基于阻抗的实时细胞和全息显微分析。我们在形态,基因和miRNA表达水平上进一步分析了AA,DHA和GLA。结果与LDH-,MTS分析和实时细胞毒性谱AA,DHA和GLA相对应,增强了神经胶质瘤细胞的放射敏感性。多不饱和脂肪酸(PUFA)和辐射的共同应用显着改变了EGR1,TNF-α,NOTCH,c-MYC,TP53,HMOX1,AKR1C1,NQO1的表达,同时上调了GADD45A,EGR1,GRP78,DDIT3,记录c-MYC,FOSL1分别响应PUFA处理或单独照射。在分析的miRNA中,miR-146和miR-181a是通过DHA处理诱导的。通过联合治疗GLA和照射,也检测到miR-146的过表达。结论由于PUFA通过生化和细胞分析评估可提高神经胶质瘤细胞的放射反应性,因此它们可能会提高放射线治疗神经胶质瘤的疗效。我们证明用DHA,AA和GLA辅助放射治疗可上调氧化应激和内质网应激相关基因的表达,并影响NOTCH1的表达,这可以解释它们的累加效应。

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