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bioRxiv · 10.64898/2026.07.15.736775

Epithelial Stem Cell Fate Determines Chemoradiotherapy Response in Rectal Cancer

Abstract

Rectal cancers are often treated with neoadjuvant chemoradiotherapy (CRT), yet 85% of patients do not achieve a pathological complete response. To identify the molecular determinants of CRT response, we profiled the single-cell signalling, DNA-damage, cell-cycle, apoptotic, and cell-fate responses of 2,769 patient-derived organoid cultures treated with CRT, cancer-associated fibroblasts (CAFs), and signal-rewiring agents. We find that CRT response is determined by stem cell-fate. CRT triggers comparable DNA-damage in isogenic proliferative (proCSC) and revival (revCSC) colonic stem cells, but proCSC retain damage and die whereas revCSC resolve damage and persist. Both CRT and CAFs drive proCSC to a common treatment-resistant revCSC fate and high revCSC predicts worse survival in patients. Pharmacologically constraining stem-cell plasticity increases CRT sensitivity, and Spatial Perturbation of ARrayed Tumour Assembloids (SPARTA) confirms YAP/TEAD inhibition improves chemotherapy responses in human stromal-tumour models. These results suggest that cancer cell-fate, not genotoxic damage itself, ultimately governs response to standard-of-care chemoradiotherapy. HIGHLIGHTSO_LIRectal cancer stem cell-fate determines chemoradiotherapy-induced apoptosis C_LIO_LIproCSCs retain DNA-damage and die, whereas revCSCs repair damage and persist C_LIO_LICAFs and chemoradiotherapy converge on a common chemo-radioresistant revCSC state C_LIO_LISPARTA reveals TEAD inhibition blocks DNA-repair persisters in stromal assembloids C_LI

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Li, N., Ishaqwala, F., Wright, T. A., Wilkinson, A., Vlckova, P., Trevers, K., O'Sullivan, R., Crampsie, S., Basiarz, E., Vanderkamp, S., McCulloch, A. K., Dobric, A., Krishnaswamy, S., Vanhaesebroeck, B., Glasgow Serial Sampling Consortium,, Roxburgh, C. S. D., Hawkins, M., Tape, C. J.. 2026-07-15. Epithelial Stem Cell Fate Determines Chemoradiotherapy Response in Rectal Cancer. https://doi.org/10.64898/2026.07.15.736775

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