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Abstract Cancer‐associated fibroblasts (CAFs) play a crucial role in the progression of pancreatic ductal adenocarcinoma (PDAC). Here, integrated single‐cell RNA sequencing analysis is utilized to comprehensively map CAFs in the human PDAC tumor microenvironment (TME). Normal fibroblasts (NFs) and nine distinct CAF subtypes are identified including newly identified CAF subtypes, CDCP1 + FTL + CAFs, transitional CAFs (tCAFs), interferon simulated genes (ISG) + myofibroblastic CAFs (myCAFs), and proliferative CAFs (pCAFs). CDCP1 + FTL + CAFs, pCAFs, and ISG + myCAFs are associated with unfavorable clinical outcomes. CDCP1 + FTL + CAFs exhibit enhanced glycolysis and iron metabolism, resisting ferroptosis. The antigen‐presenting CAFs (apCAFs) show high heterogeneity, consisting of multiple subtypes expressing distinct immune cell signatures. The CAF subtypes display differentiation plasticity, transitioning from early normal‐like CAFs (nCAFs) to inflammatory CAFs (iCAFs) and myCAFs, ultimately leading to more invasive pCAFs. AP‐1 family members FOS and JUN regulate the malignant phenotype conversion of NFs to nCAFs, while transforming growth factor‐β (TGFβ) and interferon‐γ (IFNγ) signals trigger the interconversion between classic myCAFs and iCAFs, respectively. A close interaction between CAFs and myeloid cells (especially neutrophils) is further observed in PDAC‐TME, mainly mediated by CXCR4‐CXCL12 chemotaxis. This work depicts a detailed CAF map and its dynamic interconvertible shift, providing important insights for combined targeted CAFs therapy.
Tao et al. (Fri,) studied this question.