Cellular community detection for tissue phenotyping in colorectal cancer histology images

Publikation: Beitrag in FachzeitschriftForschungsartikelBeigetragenBegutachtung

Beitragende

  • Sajid Javed - , University of Warwick, Khalifa University of Science and Technology (Autor:in)
  • Arif Mahmood - , Information Technology University (Autor:in)
  • Muhammad Moazam Fraz - , University of Warwick, National University of Sciences and Technology Pakistan (Autor:in)
  • Navid Alemi Koohbanani - , University of Warwick (Autor:in)
  • Ksenija Benes - , University Hospitals Coventry and Warwickshire NHS Trust (Autor:in)
  • Yee Wah Tsang - , University Hospitals Coventry and Warwickshire NHS Trust (Autor:in)
  • Katherine Hewitt - , University Hospitals Coventry and Warwickshire NHS Trust (Autor:in)
  • David Epstein - , University of Warwick (Autor:in)
  • David Snead - , University Hospitals Coventry and Warwickshire NHS Trust (Autor:in)
  • Nasir Rajpoot - , University of Warwick, University Hospitals Coventry and Warwickshire NHS Trust, Alan Turing Institute (Autor:in)

Abstract

Classification of various types of tissue in cancer histology images based on the cellular compositions is an important step towards the development of computational pathology tools for systematic digital profiling of the spatial tumor microenvironment. Most existing methods for tissue phenotyping are limited to the classification of tumor and stroma and require large amount of annotated histology images which are often not available. In the current work, we pose the problem of identifying distinct tissue phenotypes as finding communities in cellular graphs or networks. First, we train a deep neural network for cell detection and classification into five distinct cellular components. Considering the detected nuclei as nodes, potential cell-cell connections are assigned using Delaunay triangulation resulting in a cell-level graph. Based on this cell graph, a feature vector capturing potential cell-cell connection of different types of cells is computed. These feature vectors are used to construct a patch-level graph based on chi-square distance. We map patch-level nodes to the geometric space by representing each node as a vector of geodesic distances from other nodes in the network and iteratively drifting the patch nodes in the direction of positive density gradients towards maximum density regions. The proposed algorithm is evaluated on a publicly available dataset and another new large-scale dataset consisting of 280K patches of seven tissue phenotypes. The estimated communities have significant biological meanings as verified by the expert pathologists. A comparison with current state-of-the-art methods reveals significant performance improvement in tissue phenotyping.

Details

OriginalspracheEnglisch
Aufsatznummer101696
FachzeitschriftMedical Image Analysis
Jahrgang63
PublikationsstatusVeröffentlicht - Juli 2020
Peer-Review-StatusJa
Extern publiziertJa

Externe IDs

PubMed 32330851

Schlagworte

Ziele für nachhaltige Entwicklung

Schlagwörter

  • Cellular communities, Computational pathology, Tissue phenotyping, Tumor microenvironment