Wehbe Katia, Forfar Isabelle, Eimer Sandrine, Cinque Gianfelice
Diamond Light Source, Harwell Science and Innovation Campus, Didcot, Oxfordshire, OX11 0DE, UK.
INSERM U1034, Université Bordeaux, 33600, Pessac, France.
Anal Bioanal Chem. 2015 Sep;407(24):7295-305. doi: 10.1007/s00216-015-8891-z. Epub 2015 Jul 14.
Gliomas are brain tumours classified into four grades with increasing malignancy from I to IV. The development and the progression of malignant glioma largely depend on the tumour vascularization. Due to their tissue heterogeneity, glioma cases can be difficult to classify into a specific grade using the gold standard of histological observation, hence the need to base classification on a quantitative and reliable analytical method for accurately grading the disease. Previous works focused specifically on vascularization study by Fourier transform infrared (FTIR) spectroscopy, proving this method to be a way forward to detect biochemical changes in the tumour tissue not detectable by visual techniques. In this project, we employed FTIR imaging using a focal plane array (FPA) detector and globar source to analyse large areas of glioma tumour tissue sections via molecular fingerprinting in view of helping to define markers of the tumour grade. Unsupervised multivariate analysis (hierarchical cluster analysis and principal component analysis) of blood vessel spectral data, retrieved from the FPA images, revealed the fine structure of the borderline between two areas identified by a pathologist as grades III and IV. Spectroscopic indicators are found capable of discriminating different areas in the tumour tissue and are proposed as biomolecular markers for potential future use of grading gliomas. Graphical Abstract Infrared imaging of glioma blood vessels provides a means to revise the pathologists' line of demarcation separating grade III (GIII) from grade IV (GIV) parts.
胶质瘤是分为I至IV级的脑肿瘤,恶性程度逐渐增加。恶性胶质瘤的发生和进展在很大程度上取决于肿瘤血管生成。由于其组织异质性,使用组织学观察的金标准将胶质瘤病例准确分类到特定级别可能存在困难,因此需要基于一种定量且可靠的分析方法来对疾病进行准确分级。以往的研究专门聚焦于通过傅里叶变换红外(FTIR)光谱进行血管生成研究,证明该方法是检测肿瘤组织中视觉技术无法检测到的生化变化的有效途径。在本项目中,我们使用焦平面阵列(FPA)探测器和球形光源进行FTIR成像,通过分子指纹图谱分析大面积的胶质瘤肿瘤组织切片,以帮助确定肿瘤级别的标志物。从FPA图像中获取的血管光谱数据的无监督多变量分析(层次聚类分析和主成分分析)揭示了病理学家确定为III级和IV级的两个区域之间边界的精细结构。发现光谱指标能够区分肿瘤组织中的不同区域,并被提议作为未来胶质瘤分级潜在使用的生物分子标志物。图形摘要 胶质瘤血管的红外成像提供了一种手段来修正病理学家区分III级(GIII)和IV级(GIV)部分的分界线。