Published online Sep 7, 2026. doi: 10.3748/wjg.118185
Revised: February 25, 2026
Accepted: April 10, 2026
Published online: September 7, 2026
Processing time: 225 Days and 7.2 Hours
Previous studies have reported elevated urinary N1, N12-diacetylspermine (DiAcSpm) levels in various cancers. We therefore hypothesized that urinary DiAcSpm could serve as a potential biomarker for gastric and colorectal cancers (CRCs) and may also have prognostic value.
To assess the diagnostic potential of urinary DiAcSpm for gastric and CRC and to explore its prognostic sig
A total of 209 urine samples were collected from patients with gastrointestinal cancers, benign gastrointestinal diseases, and healthy controls. Pre- and post-treatment clinical data were obtained for all participants. Urinary DiAcSpm levels were measured using a commercially available reagent kit via an immunoturbidimetric assay on an automated biochemical analyzer.
Urinary DiAcSpm concentrations were significantly higher in patients with gastric and CRCs compared with benign disease patients and healthy controls. It discriminated gastric cancer (GC) from healthy controls with an area under the curve (AUC) of 0.714 [95% confidence interval (CI): 0.613-0.815], sensitivity of 59.65%, and specificity of 76.19%. For CRC, the AUC was 0.736 (95%CI: 0.648-0.824), with sensitivity of 42.11% and specificity of 95.24%. Combining DiAcSpm with carcinoembryonic antigen improved diagnostic performance [GC: AUC = 0.755 (95%CI: 0.657-0.852), sensitivity = 94.74%, specificity = 50.00%; CRC: AUC = 0.813 (95%CI: 0.739-0.887), sensitivity = 91.23%, specificity = 58.73%]. Urinary DiAcSpm levels significantly decreased after chemotherapy in CRC patients. High DiAcSpm levels were associated with distant metastasis in GC patients.
Urinary DiAcSpm levels are markedly elevated in patients with GC and CRC. While its standalone diagnostic accuracy requires further improvement, DiAcSpm shows promise as a complementary marker to existing serum biomarkers in combined diagnostic strategies.
Core Tip: Urinary N1, N12-diacetylspermine (DiAcSpm) was evaluated as a potential non-invasive biomarker for gastric and colorectal cancer. Levels were significantly elevated in cancer patients and showed moderate diagnostic value, which improved when combined with carcinoembryonic antigen. Urinary DiAcSpm levels decreased after chemotherapy in colorectal cancer patients, and high levels correlated with distant metastasis in gastric cancer patients. These findings support the potential of urinary DiAcSpm, though prospective studies in larger cohorts are warranted to confirm its clinical utility.