首页> 美国卫生研究院文献>Neuro-Oncology >BI-27ANALYSIS OF THE BIOCHEMICAL PROFILE OF LOW GRADE GLIOMA WITH DIFFERENT IDH1 MUTATION STATUS USING VIBRATIONAL SPECTROSCOPY
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BI-27ANALYSIS OF THE BIOCHEMICAL PROFILE OF LOW GRADE GLIOMA WITH DIFFERENT IDH1 MUTATION STATUS USING VIBRATIONAL SPECTROSCOPY

机译:振动光谱法对不同IDH1突变状态的低级胶质瘤的生物化学特征进行BI-27分析

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摘要

Mutations in human cytosolic isocitrate dehydrogenases 1 (IDH1) are a common feature of low grade gliomas (LGG) and cause profound changes of the metabolites of the Krebs cycle. Vibrational spectroscopy comprises label-free techniques that probe a sample's molecular composition. Therefore, we investigated the ability of fourier-transform infrared (FT-IR) spectroscopy to analyze the IDH1-mutation status in cell culture systems and human brain tumor samples. Cell lines (U87-MG, SVG p12 and the primary glioblastoma cell lines HT7606, HT12346 and HT12347) were transduced with either IDH1 wild-type or mutated IDH1. Clusteranalysis and principal-component-analysis were able to detect differences in the respective FT-IR spectral datasets in regions assigned to saccharides (1050 and 1120 cm−1) and proteins (1236, 1545 and 1651 cm−1). Brain tumor samples of human LGG were obtained during routine surgery and the IDH1 mutation status was determined by DNA sequencing (n = 17). Difference spectra (IDH1-mut vs. IDH1-wt) showed changes in the region around 1100 cm−1 which is attributed to saccharides. Additionally, amide I and amide II spectral bands (around 1550 and 1650 cm−1, respectively) were reduced in the IDH1-mut dataset whereas the band at 1740 cm−1 assigned to C = O stretching vibrations was more pronounced. Principal-component-analysis confirmed differences between the two groups based on spectral regions assigned to saccharides, proteins and to C = O stretching vibrations, as identified previously in the difference spectra. Supervised classification recognized relevant spectral regions at 974, 1005, 1038-1044, 1078-1082, 1267-1275, 1342, 1417-1421, 1479 cm−1 and was able to assign 16 of the 17 tumor samples to the correct group. On the basis of FT-IR spectroscopy samples of LGG carrying IDH1 mutations can be discerned from IDH1 wildtype tumors. Relevant spectral regions assigned to saccharides and C = O stretching vibrations can be explained by changes in the Krebs cycle and in particular by the accumulation of 2-hydroxyglutarate (rich in C = O bonds).
机译:人胞质异柠檬酸脱氢酶1(IDH1)中的突变是低级神经胶质瘤(LGG)的共同特征,并引起克雷布斯循环代谢产物的深刻变化。振动光谱法包括探测样品分子组成的无标记技术。因此,我们研究了傅里叶变换红外(FT-IR)光谱分析细胞培养系统和人脑肿瘤样品中IDH1突变状态的能力。用IDH1野生型或突变的IDH1转导细胞系(U87-MG,SVG p12和原发​​性胶质母细胞瘤细胞系HT7606,HT12346和HT12347)。聚类分析和主成分分析能够检测到分配给糖(1050和1120 cm -1 )和蛋白质(1236、1545和1651 cm < sup> -1 )。在常规手术中获得了人类LGG的脑肿瘤样品,并通过DNA测序确定了IDH1突变状态(n = 17)。差异光谱(IDH1-mut vs. IDH1-wt)显示了在1100 cm -1 周围区域的变化,这归因于糖类。此外,IDH1-mut数据集中的酰胺I和酰胺II光谱带(分别在1550和1650 cm -1 处)减少,而在1740 cm -1 处的波段降低。分配给C = O的拉伸振动更为明显。主成分分析基于分配给糖类,蛋白质和C = O拉伸振动的光谱区域确认了两组之间的差异,如先前在差异光谱中所确定的。监督分类识别了974、1005、1038-1044、1078-1082、1267-1275、1342、1417-1421、1479 cm -1 的相关光谱区域,并能够分配17个肿瘤中的16个采样到正确的组。基于FT-IR光谱,可以从IDH1野生型肿瘤中识别出携带IDH1突变的LGG样品。分配给糖类和C = O拉伸振动的相关光谱区域可以通过Krebs循环的变化来解释,尤其可以通过2-羟基戊二酸的积累(富含C = O键)来解释。

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