ArticleCell reports. Medicine2026
DeCAF defines clinical fibroblast subtypes and multidimensional tumor-stroma crosstalk shaping prognosis and immunotherapy response.
Article in Cell reports. Medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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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
4 citing papers in PubMed.
- Targeting cancer-associated fibroblasts: therapeutic strategies, translational challenges, and future perspectives.Journal of hematology & oncology · 2026Review
- Role of the stromal and immune microenvironment in intrahepatic cholangiocarcinoma.JHEP reports : innovation in hepatology · 2026Review
- Single-cell profiling reveals a novel CAF subpopulation linking stromal heterogeneity to immune suppression in breast cancer subtypes.Journal of translational medicine · 2026Article
- Characterizing pancreatic cancer-associated fibroblast heterogeneity in vascular microphysiological systems.Angiogenesis · 2026Article
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28 authors.
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Abstract
Single-cell RNA sequencing (scRNA-seq) studies have uncovered distinct cancer-associated fibroblast (CAF) populations. While useful as a biological framework, no studies have conclusively defined CAF subtypes with clinical significance. We define restraining (rest) and promoting (pro) CAFs in patient samples that are both prognostic and predictive of therapy response in multiple tumor types. We uncover distinct clinical and spatial interactions between pro- and restCAF subtypes and basal-like and classical tumor subtypes that support tumor-stroma crosstalk. Finally, we find striking differences in the immune contexture of pro- and restCAF tumors where restCAF-dominant tumors are more responsive to immune checkpoint inhibition and proCAF-dominant tumors are more responsive to myeloid inhibition in clinical trials. This work defines CAF subtypes that are clinically robust, prognostic, and predictive of immunotherapy response and provides a single-sample classifier, determination of pro- and restCAF subtypes (DeCAF), which is clinically actionable.
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Registered trials
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