bioRxiv · 10.64898/2026.06.05.730533
Early detection of pancreatic ductal adenocarcinoma by single-molecule profiling of pancreatic enzyme activities
Abstract
Pancreatic ductal adenocarcinoma (PDAC) remains a leading cause of cancer-related mortality, largely due to diagnosis at advanced stages. Early detection through minimally invasive liquid biopsy holds promise for improving patient outcomes. Here, we report a blood-based liquid biopsy platform based on single-molecule enzyme activity profiling (SEAP), which detects proteoform-level alterations in circulating pancreatic enzymes at single-molecule resolution. Using a tissue-centric biomarker discovery strategy, we identified activity signatures of pancreas-specific digestive enzymes associated with PDAC. A combinatorial classifier detected PDAC (stage I-IV) with 95.5% specificity and 75.0% sensitivity (74.2% for stage I-II) across 690 blood samples collected from multiple hospitals and biobanks. Performance was further validated in an independent cohort enriched for early-stage disease, where 54.2% (13/24) of stage IA, 64.3% (9/14) of stage IB, and 21.4% (3/14) of stage 0 lesions were classified as positive. These findings support the clinical potential of SEAP for early detection of PDAC.
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Sakamoto, S., Hiraide, H., Hatakeyama, J., Kobayashi, T., Takahashi, K., Inagaki, T., Takagi-Niidome, S., Minoda, M., Kawaguchi, T., Shibayama, T., Iwakura, N., Kawana, M., Mizuno, T., Kawaguchi, M., Nakagawa, H., Fujita, K., Urano, Y., Masuda, A., Ikemoto, J., Ishii, Y., Oka, S., Hanada, K., Kodama, Y., Komatsu, T., Kagami, Y.. 2026-06-09. Early detection of pancreatic ductal adenocarcinoma by single-molecule profiling of pancreatic enzyme activities. https://doi.org/10.64898/2026.06.05.730533
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