Label-Free Deep Profiling of the Tumor Microenvironment

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

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.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Computational Biology / methods*
  • Endothelial Cells / metabolism
  • Erythrocytes / metabolism
  • Extracellular Vesicles / metabolism
  • Female
  • Fibroblasts / metabolism
  • Lymphocytes / metabolism
  • Mammary Neoplasms, Experimental / diagnostic imaging*
  • Mammary Neoplasms, Experimental / metabolism
  • Mammary Neoplasms, Experimental / pathology
  • Mice
  • Neural Networks, Computer
  • Nonlinear Optical Microscopy / methods*
  • Optical Imaging
  • Rats
  • Rats, Inbred WF
  • Single-Cell Analysis / methods
  • Tumor Microenvironment*