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bioRxiv · 10.64898/2026.07.09.737397

Pan-cancer single-cell analysis identifies a FOXF1/FOXF2-associated transitional CAF-like fibroblast state

Mandzhieva, B.·Verma, A.·Nguyen, T. D. T.·Bang, Y. H.·Park, W. Y.
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Abstract

Fibroblast heterogeneity shapes tumor progression, yet the transitional states linking normal-associated fibroblasts to cancer-associated fibroblasts (CAFs) remain poorly defined. Here, we integrated single-cell transcriptomic profiles of more than 90,000 stromal cells from 281 samples across nine cancer types to construct a pan-cancer atlas of fibroblast diversity. We identified a distinct CAF-like population positioned between normal-activated fibroblasts and established CAF subsets along the inferred fibroblast activation trajectory. Integration with single-nucleus chromatin accessibility data nominated FOXF1 and FOXF2 as candidate regulators of this CAF-like state. Functionally, CAF-like fibroblasts were characterized by non-canonical WNT activity, WNT5A-associated stromal communication, and a candidate GZMA-F2R/PAR immune-stromal signaling axis supported by spatial transcriptomics. Clinically, the CAF-like signature showed context-dependent prognostic relevance, with high expression associated with poorer survival in the tumor compartment of TCGA stomach adenocarcinoma. Together, this study defines a FOXF1/FOXF2-associated CAF-like transitional fibroblast state and links it to stromal signaling, immune-stromal communication, and cancer-type-specific clinical relevance.

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Mandzhieva, B., Verma, A., Nguyen, T. D. T., Bang, Y. H., Park, W. Y.. 2026-07-10. Pan-cancer single-cell analysis identifies a FOXF1/FOXF2-associated transitional CAF-like fibroblast state. https://doi.org/10.64898/2026.07.09.737397

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