Discriminating healthy from tumor and necrosis tissue in rat brain tissue samples by Raman spectral imaging

被引:80
作者
Amharref, Nadia
Bejebbar, Abdelilah
Dukie, Sylvain
Venteo, Lydie
Schneider, Laurence
Pluot, Michel
Manfait, Michel
机构
[1] Univ Reims, IFR 53, UFR Pharm, Unite MeDIAN,CNRS,UMR 6142, F-51096 Reims, France
[2] CHU Robert Debre, Lab Cent Anat & Cytol Pathol, F-51092 Reims, France
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2007年 / 1768卷 / 10期
关键词
Raman imaging; glioma; invasion; necrosis; brain structure; edema;
D O I
10.1016/j.bbamem.2007.06.032
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
The purpose of this study was to investigate molecular changes associated with glioma tissues by Raman microspectroscopy in order to develop its use in clinical practice. Spectroscopic markers obtained from C6 glioma tissues were compared to conventional histological and histochemical techniques. Cholesterol and phospholipid contents were highest in corpus callosum and decreased gradually towards the cortex surface as well as in the tumor. Two different necrotic areas have been identified: a fully necrotic zone characterized by the presence of plasma proteins and a peri-necrotic area with a high lipid content. This result was confirmed by Nile Red staining. Additionally, one structure was detected in the periphery of the tumor. Invisible with histopathological hematoxylin and eosin staining, it was revealed by immunohistochemical Ki-67 and MTI-MMP staining used to visualize the proliferative and invasive activities of glioma, respectively. Hierarchical cluster analysis on the only cluster averaged spectra showed a clear distinction between normal, tumoral, necrotic and edematous tissues. Raman microspectroscopy can discriminate between healthy and tumoral brain tissue and yield spectroscopic markers associated with the proliferative and invasive properties of glioblastoma. Development of in vivo Raman spectroscopy could thus accurately define tumor margins, identify tumor remnants, and help in the development of novel therapies for glioblastoma. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:2605 / 2615
页数:11
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