MéDIAN Biophotonique et Technologies pour la Santé, Université de Reims Champagne-Ardenne, FRE CNRS 3481 MEDyC, UFR de Pharmacie, SFR Cap Santé, 51096 Reims Cedex, France.
Cytometry A. 2013 Mar;83(3):294-300. doi: 10.1002/cyto.a.22249. Epub 2013 Jan 9.
Complementary diagnostic methods to conventional histopathology are under scrutiny for various types of cancers for rapid and molecular level diagnostics. In this perspective, a biophotonic approach based on infrared spectral micro-imaging combined with multivariate statistical analysis has been implemented on colon tissues. The ability of infrared imaging to investigate the intrinsic biochemical features of cells and tissues has been exploited to develop a new concept of spectral bar coding. To implement this concept, 10 frozen colon tissue samples (five nontumoral and tumoral pairs from five patients) were imaged using infrared spectral micro-imaging in a nondestructive manner. The spectral images were processed by a multivariate clustering method to identify the histological organization in a label-free manner. Spectral information from the epithelial components was then automatically recovered on the basis of their intrinsic biochemical composition, and compared using a statistical method (Mann-Whitney U-test) to construct spectral barcodes specific to each patient. The spectral barcodes representing the discriminant infrared spectral wavenumbers (900-1,800 cm(-1) ) enabled characterization of some of the malignancy-associated biochemical alterations associated with mucin, nucleotides, carbohydrates, and protein regions. This approach not only allowed the identification of common biochemical alterations among all the colon cancer patients, but also revealed a difference of gradient within individual patients. This new concept of spectral bar coding gives insight into the potential of infrared spectral micro-imaging as a complementary diagnostic tool to conventional histopathology, for biochemical level understanding of malignancy in colon cancers in an objective and label-free manner.
补充诊断方法,以传统的组织病理学是在审查各种类型的癌症的快速和分子水平的诊断。从这个角度来看,一个基于生物光子学的方法,基于红外光谱的微观成像与多元统计分析已经实施了结肠组织。红外成像能力调查的内在生化特征的细胞和组织已经被利用来开发一个新的概念,光谱条形码。为了实现这一概念,10 个冷冻的结肠组织样本(五个非肿瘤和肿瘤对从五个病人)进行成像用红外光谱微观成像以非破坏性的方式。光谱图像进行了多元聚类方法来识别组织学的组织在一个无标签的方式。光谱信息从上皮成分,然后自动恢复基于其内在的生化组成,并比较用统计方法(Mann-Whitney U 检验)来构建光谱条形码特定的每个病人。光谱条形码代表的判别红外光谱波数(900-1800 厘米(-1))能够表征的一些与粘蛋白,核苷酸,碳水化合物,和蛋白质的区域相关的恶性相关的生化改变。这种方法不仅可以识别所有结肠癌患者常见的生化变化,但也揭示了梯度之间的差异内的个体病人。这种新的概念的光谱条形码提供了深入的潜力,作为一个补充的诊断工具,以传统的组织病理学,生化水平的理解的恶性肿瘤在结肠癌以客观和无标签的方式。