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GC-MS-based metabolomics analysis of 3,2-trans-enoyl-CoA isomerase knockdown mutants in human hepatoma cells

机译:基于GC-MS的代谢组合分析人肝癌细胞3,2-反式烯库 - COA异构酶敲低突变体

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732 features were identified by matching the GC-MS data to entries in the Fiehn Metabolomics RTL Library. 37 metabolites were identified as having significant differences (q < 0.05) in abundance among the four cell types based on ANOVA, while a G-test analysis identified an additional 64 metabolites as significantly different (p < 0.05) based on occurrence. Most amino acids and their derivatives, fatty acids, sugars, and vitamins were increased in DCI-1 knockdown cells relative to the other three cell types, while nucleobases and aromatic metabolites were decreased. Increases in amino acids and intermediates of urea synthesis are consistent with multiple fatty acid oxidation deficient mouse models and suggest an increased dependence on amino acids for energy production in the absence of mitochondrial beta-oxidation of fatty acids.
机译:通过将GC-MS数据与Fiehn代谢组合RTL库中的条目匹配来识别732个功能。 37代谢物被鉴定为基于ANOVA的四种细胞类型的丰富具有显着差异(Q <0.05),而G-Test分析鉴定了另外的64种代谢物,显着不同(P <0.05)基于发生。 在DCI-1敲低细胞相对于其他三种细胞类型中,大多数氨基酸及其衍生物,脂肪酸,糖和维生素增加,而核碱基和芳族代谢物减少。 氨基酸和尿素合成中间体的增加与多种脂肪酸氧化不足小鼠模型一致,并表明在没有线粒体β-氧化脂肪酸的情况下对能量产生的氨基酸增加依赖性。

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