The single-cell spatial landscape of stage III colorectal cancers

We conducted a spatial analysis of stage III colorectal adenocarcinomas using Hyperion Imaging Mass Cytometry, examining 52 tumors to assess the tumor microenvironment at the single-cell level. This approach identified 10 distinct cell phenotypes in the tumor microenvironment, including stromal and immune cells, with a subset showing a proliferative phenotype. By focusing on spatial neighborhood interactions and tissue niches, particularly regions with tumor-infiltrating lymphocytes, we investigated how cellular organization relates to clinicopathological and molecular features such as microsatellite instability (MSI) and recurrence. We determined that microsatellite stable (MSS) colorectal cancers had an increased risk of recurrence if they had the following features: 1) a low level of stromal tumor-infiltrating lymphocytes, and 2) low interactions between CD4 + T cells and stromal cells. Our results point to the utility of spatial single-cell interaction analysis in defining novel features of the tumor immune microenvironments and providing useful clinical cell-related spatial biomarkers.

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Publication Details

Journal
npj Precision Oncology
Published
2025-04-06
DOI
https://doi.org/10.1038/s41698-025-00853-5
Citations
7
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
5.64

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article

The single-cell spatial landscape of stage III colorectal cancers

Xiangqi Bai, Ignacio Wichmann, Anuja Sathe, Terence D. Rhodes et al.
7 citations
npj Precision Oncology
Single-cell and spatial transcriptomics
5.64
article

The single-cell spatial landscape of stage III colorectal cancers

Xiangqi Bai, Ignacio Wichmann, Anuja Sathe, Terence D. Rhodes, Richard Cruz, Quan Nguyen, Lincoln Nadauld, Hanlee P. Ji, Lance Pflieger, HoJoon Lee, Bryce Moulton, Andrew Su, Derrick S. Haslem, David A. Jones, Minh Tran, Tyler Barker
article en
7 citations

Abstract

We conducted a spatial analysis of stage III colorectal adenocarcinomas using Hyperion Imaging Mass Cytometry, examining 52 tumors to assess the tumor microenvironment at the single-cell level. This approach identified 10 distinct cell phenotypes in the tumor microenvironment, including stromal and immune cells, with a subset showing a proliferative phenotype. By focusing on spatial neighborhood interactions and tissue niches, particularly regions with tumor-infiltrating lymphocytes, we investigated how cellular organization relates to clinicopathological and molecular features such as microsatellite instability (MSI) and recurrence. We determined that microsatellite stable (MSS) colorectal cancers had an increased risk of recurrence if they had the following features: 1) a low level of stromal tumor-infiltrating lymphocytes, and 2) low interactions between CD4 + T cells and stromal cells. Our results point to the utility of spatial single-cell interaction analysis in defining novel features of the tumor immune microenvironments and providing useful clinical cell-related spatial biomarkers.

npj Precision OncologyVol. 9(1)
Intermountain Healthcare (US), Pontificia Universidad Católica de Chile (CL), The University of Queensland (AU), Stanford University (US)
Intermountain Healthcare, National Institutes of Health, Medical Research Council, National Health and Medical Research Council
Good health and well-being
Openalex Percentile: Top 4%
Single-cell and spatial transcriptomics
5.64
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