ArticleGenes & diseases2026
Dynamic single-cell landscape reveals a T-cell-suppressed microenvironment and a conserved neutrophil program in the lung metastatic niche.
Article in Genes & diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
1 citing paper in PubMed.
- cGAS-STING signaling in aging and age-related diseases: therapeutic promise and precaution.Archives of pharmacal research · 2026Review
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Authors and funding
16 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
While the immune landscape of primary tumors is increasingly understood, the dynamic immune remodeling within the evolving lung metastatic microenvironment remains poorly characterized. Here, by systematically comparing the microenvironments of primary and metastatic tumors using single-cell transcriptomics across diverse cancer models, we reveal that lung metastases consistently establish a profoundly T-cell-suppressed microenvironment. Concurrently, we identified a strictly metastasis-specific neutrophil gene program. Crucially, this program is highly concurrent with the metastatic microenvironment and is fundamentally distinct from neutrophil phenotypes observed in primary tumors or healthy lungs. Among the core genes defining this program, we identified the cell surface marker STEAP4 as a highly specific indicator of these metastasis-associated neutrophils. In both murine models and human patients, these STEAP4
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