bioRxiv · 10.64898/2026.04.02.716182
Integrated analysis of stemness-associated immune modulatory circuits in squamous cell carcinomas
Abstract
Emerging evidence indicates that a subset of cancer cells enriched for stemness-related gene signatures possess distinct immunomodulatory capacities, enabling these tumor-initiating stem cells (tSCs) to more effectively evade or resist anti-tumor immunity. Despite these advances, the tSC-specific molecular circuits orchestrating their specialized immune privilege program are not well defined. Here, in squamous cell carcinomas of the skin and oral cavity, we comprehensively delineate the unique immune-evasive properties of tSCs and dissect the transcriptional regulation shaping their immunomodulatory programs. By integrating transcriptome profiling, chromatin landscape mapping, genetic perturbation, and single-cell RNA sequencing, we found that the tSC-specific immune program is broadly governed by SOX2, a stemness-associated transcription factor. We demonstrate that SOX2 enables tSCs to sustain immature tumor-associated neutrophils (TANs) and subsequently trigger these myeloid cells to foster the development of tumor-associated macrophages (TAMs). This SOX2-directed tSC-TAN-TAM axis establishes a localized immunosuppressive niche for protecting tSC. SIGNIFICANCEHere, we uncover SOX2 as a master regulator that orchestrates conserved immune modulatory circuits in tSCs to sustain pro-tumor myeloid cell states. These findings place tSCs at the apex of immune landscape remodeling, asserting a central role of stemness-associated program in organizing the immunosuppressive tumor microenvironment.
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Guo, W., Leon, D., Luan, J., Gang, A., Huang, X., Nicholson, B., Dorosz, K., Zhao, Y. S., Grimshaw, S., Bolotin, D., Lingen, M. W., Vokes, E. E., Pearson, A., Rosenberg, A. J., Shen, L., Izumchenko, E., Agrawal, N., Jiang, J., Miao, Y. P.. 2026-04-06. Integrated analysis of stemness-associated immune modulatory circuits in squamous cell carcinomas. https://doi.org/10.64898/2026.04.02.716182
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