IBM Research Europe, Zurich, Rüschlikon, Switzerland.
Department of Pathology and Molecular Pathology, University Hospital Zurich and University Zurich, Zurich, Switzerland.
PLoS One. 2021 Nov 19;16(11):e0259332. doi: 10.1371/journal.pone.0259332. eCollection 2021.
A new workflow for protein-based tumor heterogeneity probing in tissues is here presented. Tumor heterogeneity is believed to be key for therapy failure and differences in prognosis in cancer patients. Comprehending tumor heterogeneity, especially at the protein level, is critical for tracking tumor evolution, and showing the presence of different phenotypical variants and their location with respect to tissue architecture. Although a variety of techniques is available for quantifying protein expression, the heterogeneity observed in the tissue is rarely addressed. The proposed method is validated in breast cancer fresh-frozen tissues derived from five patients. Protein expression is quantified on the tissue regions of interest (ROI) with a resolution of up to 100 μm in diameter. High heterogeneity values across the analyzed patients in proteins such as cytokeratin 7, β-actin and epidermal growth factor receptor (EGFR) using a Shannon entropy analysis are observed. Additionally, ROIs are clustered according to their expression levels, showing their location in the tissue section, and highlighting that similar phenotypical variants are not always located in neighboring regions. Interestingly, a patient with a phenotype related to increased aggressiveness of the tumor presents a unique protein expression pattern. In summary, a workflow for the localized extraction and protein analysis of regions of interest from frozen tissues, enabling the evaluation of tumor heterogeneity at the protein level is presented.
这里提出了一种用于组织中基于蛋白质的肿瘤异质性探测的新工作流程。肿瘤异质性被认为是癌症患者治疗失败和预后差异的关键。理解肿瘤异质性,特别是在蛋白质水平上,对于跟踪肿瘤进化以及显示不同表型变体的存在及其相对于组织架构的位置至关重要。尽管有多种技术可用于定量蛋白质表达,但组织中观察到的异质性很少得到解决。该方法在来自五名患者的乳腺癌新鲜冷冻组织中进行了验证。使用香农熵分析,在直径高达 100μm 的组织感兴趣区域 (ROI) 上定量蛋白质表达。在分析的患者中,观察到细胞角蛋白 7、β-肌动蛋白和表皮生长因子受体 (EGFR) 等蛋白质的高度异质性值。此外,根据它们的表达水平对 ROI 进行聚类,显示它们在组织切片中的位置,并突出表明,相似的表型变体并不总是位于相邻区域。有趣的是,具有与肿瘤侵袭性增加相关表型的患者表现出独特的蛋白质表达模式。总之,提出了一种从冷冻组织中提取和分析感兴趣区域的局部化工作流程,能够在蛋白质水平上评估肿瘤异质性。