TY - JOUR
T1 - Urine cf-nucleosomes
T2 - A non-invasive window into human physiology and disease
AU - Lotem, Matan
AU - Sharkia, Israa
AU - Azria, Batia
AU - Harpenas, Esther
AU - Ormianer, Maayan
AU - Rosen, Hadar
AU - Falick-Michaeli, Tal
AU - Friedman, Nir
N1 - Publisher Copyright:
© 2025 The Authors
PY - 2025/10/8
Y1 - 2025/10/8
N2 - Urine contains fragments of cell-free DNA (cfDNA) that offer molecular insights into processes within the urinary system and the body. It remains unclear whether these fragments exist as chromatin and retain chromatin modifications from their cells of origin. Here, we employ cell-free chromatin immunoprecipitation followed by sequencing (cfChIP-seq) on human urine to address this issue. We show that cf-nucleosomes can be captured from urine and preserve histone modifications associated with gene activation and repression. Analysis in healthy individuals reveals distinct tissue contributions to urine cf-nucleosomes, including a kidney-derived population not detected in matched exfoliated cells or plasma. This suggests that kidney filtration largely excludes plasma cf-nucleosomes. In patients with bladder cancer, urine cf-nucleosomes reflect tumor-associated transcriptional programs and immune responses. These findings highlight the utility of urine cf-nucleosomes as accessible, non-invasive biomarkers for studying renal physiology and monitoring urinary pathologies.
AB - Urine contains fragments of cell-free DNA (cfDNA) that offer molecular insights into processes within the urinary system and the body. It remains unclear whether these fragments exist as chromatin and retain chromatin modifications from their cells of origin. Here, we employ cell-free chromatin immunoprecipitation followed by sequencing (cfChIP-seq) on human urine to address this issue. We show that cf-nucleosomes can be captured from urine and preserve histone modifications associated with gene activation and repression. Analysis in healthy individuals reveals distinct tissue contributions to urine cf-nucleosomes, including a kidney-derived population not detected in matched exfoliated cells or plasma. This suggests that kidney filtration largely excludes plasma cf-nucleosomes. In patients with bladder cancer, urine cf-nucleosomes reflect tumor-associated transcriptional programs and immune responses. These findings highlight the utility of urine cf-nucleosomes as accessible, non-invasive biomarkers for studying renal physiology and monitoring urinary pathologies.
KW - ChIP-seq
KW - bladder cancer
KW - chromatin immunoprecipitation followed by sequencing
KW - epigenomics
KW - glomerular filtration
KW - histone post-translational modifications
KW - non-invasive molecular assays
KW - urinary cell-free DNA
UR - https://www.scopus.com/pages/publications/105013237815
U2 - 10.1016/j.xgen.2025.100974
DO - 10.1016/j.xgen.2025.100974
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C2 - 40816280
AN - SCOPUS:105013237815
SN - 2666-979X
VL - 5
JO - Cell Genomics
JF - Cell Genomics
IS - 10
M1 - 100974
ER -