Stefanakis Mona, Bassler Miriam C, Walczuch Tobias R, Gerhard-Hartmann Elena, Youssef Almoatazbellah, Scherzad Agmal, Stöth Manuel Bernd, Ostertag Edwin, Hagen Rudolf, Steinke Maria R, Hackenberg Stephan, Brecht Marc, Meyer Till Jasper
Process Analysis and Technology (PA&T), Reutlingen University, Alteburgstr. 150, 72762 Reutlingen, Germany.
Institute of Physical and Theoretical Chemistry, University of Tübingen, Auf der Morgenstelle 18, 72076 Tübingen, Germany.
J Clin Med. 2023 Jan 10;12(2):569. doi: 10.3390/jcm12020569.
Due to the wide variety of benign and malignant salivary gland tumors, classification and malignant behavior determination based on histomorphological criteria can be difficult and sometimes impossible. Spectroscopical procedures can acquire molecular biological information without destroying the tissue within the measurement processes. Since several tissue preparation procedures exist, our study investigated the impact of these preparations on the chemical composition of healthy and tumorous salivary gland tissue by Fourier-transform infrared (FTIR) microspectroscopy. Sequential tissue cross-sections were prepared from native, formalin-fixed and formalin-fixed paraffin-embedded (FFPE) tissue and analyzed. The FFPE cross-sections were dewaxed and remeasured. By using principal component analysis (PCA) combined with a discriminant analysis (DA), robust models for the distinction of sample preparations were built individually for each parotid tissue type. As a result, the PCA-DA model evaluation showed a high similarity between native and formalin-fixed tissues based on their chemical composition. Thus, formalin-fixed tissues are highly representative of the native samples and facilitate a transfer from scientific laboratory analysis into the clinical routine due to their robust nature. Furthermore, the dewaxing of the cross-sections entails the loss of molecular information. Our study successfully demonstrated how FTIR microspectroscopy can be used as a powerful tool within existing clinical workflows.
由于涎腺良恶性肿瘤种类繁多,基于组织形态学标准进行分类和确定恶性行为可能会很困难,有时甚至无法做到。光谱学方法可以在测量过程中不破坏组织的情况下获取分子生物学信息。由于存在多种组织制备程序,我们的研究通过傅里叶变换红外(FTIR)显微光谱法研究了这些制备方法对健康和肿瘤性涎腺组织化学成分的影响。从新鲜组织、福尔马林固定组织和福尔马林固定石蜡包埋(FFPE)组织制备连续的组织横截面并进行分析。对FFPE横截面进行脱蜡并重新测量。通过使用主成分分析(PCA)结合判别分析(DA),针对每种腮腺组织类型分别建立了区分样品制备的稳健模型。结果,PCA-DA模型评估显示新鲜组织和福尔马林固定组织在化学成分上具有高度相似性。因此,福尔马林固定组织高度代表新鲜样品,并且由于其稳健的性质,便于从科学实验室分析转化为临床常规操作。此外,横截面的脱蜡会导致分子信息的丢失。我们的研究成功证明了FTIR显微光谱法如何能够在现有的临床工作流程中作为一种强大的工具使用。