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无标记深度剖析肿瘤微环境。

Label-Free Deep Profiling of the Tumor Microenvironment.

机构信息

Beckman Institute for Advanced Science and Technology, University of Illinois at Urbana-Champaign, Urbana, Illinois.

Department of Bioengineering, University of Illinois at Urbana-Champaign, Urbana, Illinois.

出版信息

Cancer Res. 2021 May 1;81(9):2534-2544. doi: 10.1158/0008-5472.CAN-20-3124. Epub 2021 Mar 19.

DOI:10.1158/0008-5472.CAN-20-3124
PMID:33741692
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8137645/
Abstract

Label-free nonlinear microscopy enables nonperturbative visualization of structural and metabolic contrast within living cells in their native tissue microenvironment. Here a computational pipeline was developed to provide a quantitative view of the microenvironmental architecture within cancerous tissue from label-free nonlinear microscopy images. To enable single-cell and single-extracellular vesicle (EV) analysis, individual cells, including tumor cells and various types of stromal cells, and EVs were segmented by a multiclass pixelwise segmentation neural network and subsequently analyzed for their metabolic status and molecular structure in the context of the local cellular neighborhood. By comparing cancer tissue with normal tissue, extensive tissue reorganization and formation of a patterned cell-EV neighborhood was observed in the tumor microenvironment. The proposed analytic pipeline is expected to be useful in a wide range of biomedical tasks that benefit from single-cell, single-EV, and cell-to-EV analysis. SIGNIFICANCE: The proposed computational framework allows label-free microscopic analysis that quantifies the complexity and heterogeneity of the tumor microenvironment and opens possibilities for better characterization and utilization of the evolving cancer landscape.

摘要

无标记非线性显微镜能够在活细胞的天然组织微环境中对结构和代谢对比度进行非侵入性可视化。在这里,开发了一种计算流程,可从无标记非线性显微镜图像中提供癌症组织内微环境结构的定量视图。为了能够进行单细胞和单个细胞外囊泡 (EV) 分析,通过多类像素级分割神经网络对单个细胞(包括肿瘤细胞和各种类型的基质细胞)和 EV 进行分割,然后根据局部细胞邻域分析其代谢状态和分子结构。通过将癌症组织与正常组织进行比较,在肿瘤微环境中观察到广泛的组织重排和图案化的细胞-EV 邻域形成。所提出的分析流程有望在广泛的生物医学任务中有用,这些任务受益于单细胞、单个 EV 和细胞-EV 分析。意义:所提出的计算框架允许进行无标记的显微镜分析,该分析可以量化肿瘤微环境的复杂性和异质性,并为更好地描述和利用不断发展的癌症景观开辟了可能性。

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