Single-cell profiling of bone metastasis ecosystems from multiple cancer types reveals convergent and divergent mechanisms of bone colonization

Bone is a common site for metastasis of solid cancers. The diversity of histological and molecular characteristics of bone metastases (BMs) remains poorly studied. Here, we performed single-cell RNA sequencing on 42 BMs from eight cancer types, identifying three distinct ecosystem archetypes, each characterized by an enrichment of specific immune cells: macrophages/osteoclasts, regulatory/exhausted T cells, or monocytes. We validated these archetypes by immunostaining on tissue sections and bioinformatic analysis of bulk RNA sequencing/microarray data from 158 BMs across more than 10 cancer types. Interestingly, we found only a modest correlation between the BM archetypes and the tissues of origin; BMs from the same cancer type often fell into different archetypes, while BMs from different cancer types sometimes converged on the same archetype. Additional analyses revealed parallel immunosuppression and bone remodeling mechanisms, some of which were experimentally validated. Overall, we discovered unappreciated heterogeneity of BMs across different cancers.

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Publication Details

Journal
Cell Genomics
Published
2025-05-23
DOI
https://doi.org/10.1016/j.xgen.2025.100888
Citations
9
Primary Topic
Cancer Cells and Metastasis
Type
article
Field-Weighted Citation Impact
9.41
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article

Single-cell profiling of bone metastasis ecosystems from multiple cancer types reveals convergent and divergent mechanisms of bone colonization

Yi-Hsuan Wu, Yichao Shen, Sergio Aguirre, George Miles et al.
9 citations
Cell Genomics
Cancer Cells and Metastasis
9.41
article

Single-cell profiling of bone metastasis ecosystems from multiple cancer types reveals convergent and divergent mechanisms of bone colonization

Yi-Hsuan Wu, Yichao Shen, Sergio Aguirre, George Miles, Zbigniew Gugala, Hilda L. Chan, Luis Becerra Dominguez, Dane K. Hoffman, Yang Gao, Yunfeng Ding, Robert L. Satcher, Siyue Wang, Michael Warren Dieffenbach, Tianhong Pan, Liqun Yu, David G. Edwards, Xiang Chen, Igor Bado, Xiang H.-F. Zhang, Ling Wu, Zhan Xu, Charlotte Helena Rivas, Xiaoxin Hao, Weijie Zhang, Hai Wang, Junping Liu, Fengshuo Liu, Elina Chen
article en
9 citations

Abstract

Bone is a common site for metastasis of solid cancers. The diversity of histological and molecular characteristics of bone metastases (BMs) remains poorly studied. Here, we performed single-cell RNA sequencing on 42 BMs from eight cancer types, identifying three distinct ecosystem archetypes, each characterized by an enrichment of specific immune cells: macrophages/osteoclasts, regulatory/exhausted T cells, or monocytes. We validated these archetypes by immunostaining on tissue sections and bioinformatic analysis of bulk RNA sequencing/microarray data from 158 BMs across more than 10 cancer types. Interestingly, we found only a modest correlation between the BM archetypes and the tissues of origin; BMs from the same cancer type often fell into different archetypes, while BMs from different cancer types sometimes converged on the same archetype. Additional analyses revealed parallel immunosuppression and bone remodeling mechanisms, some of which were experimentally validated. Overall, we discovered unappreciated heterogeneity of BMs across different cancers.

Cell GenomicsVol. 5(7)
The University of Texas MD Anderson Cancer Center (US), Baylor College of Medicine (US), The University of Texas Medical Branch at Galveston (US), The University of Texas at Austin (US)
Openalex Percentile: Top 2%
Cancer Cells and Metastasis
9.41
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