ArticleScientific reports2025
Plasma-based digital PCR assay for early detection of gastric cancer using multiple methylation biomarkers.
Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed.
- Exploratory profiling of oxidative stress and hydrogen sulfide synthesis gene expression and sequence variants in gastric cancer patients.Molecular biology reports · 2026Article
- Research advances in the role of circulating microorganisms in gastrointestinal tumors (Review).Molecular and clinical oncology · 2026Review
- Molecular Mechanisms and Biomarkers Driving the Transition From Chronic Atrophic Gastritis to Gastric Cancer.Clinical Medicine Insights. Oncology · 2026Review
- From Tumor Biology to Clinical Perspectives: Novel Biomarkers and Therapeutic Insights in Gastric Cancer.Oncology research · 2026Review
- Identification of an m7G-Related lncRNA Signature for Prognostic Prediction and Immune Landscape Characterization in Early Gastric Cancer.OncoTargets and therapy · 2026Article
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Authors and funding
5 authors.
Funding
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Abstract
Endoscopy is the gold standard for diagnosing gastric cancer (GC), but its invasiveness limits widespread participation and has not substantially reduced GC-related mortality. This study developed and validated a blood-based digital PCR assay for early GC detection using DNA methylation biomarkers. Genome-wide methylation profiles from over 10,000 samples were screened, and two candidates were validated in GC cell lines, tumors, matched non-cancerous tissues, and plasma. Plasma from 60 GC patients, including 38 with stage I disease, and 40 healthy controls was analyzed with a digital PCR assay targeting the selected biomarkers, using ACTB as a reference. GHR and GLRB methylation were identified as novel GC biomarkers, showing consistent hypermethylation in GC cell lines and tumor tissues. In plasma, the two-marker assay achieved 83.3% (95% CI 71.5%-91.7%) sensitivity and 90% (95% CI 76.3%-97.2%) specificity, clearly outperforming carcinoembryonic antigen (CEA) testing (10.0%; 95% CI 3.8%-20.5%). Incorporation of GATM methylation as a third marker increased sensitivity to 86.7% (95% CI 75.4%-94.1%) overall and 81.6% (95% CI 65.7%-92.3%) for stage I disease, while maintaining 90.0% specificity. This methylation-based digital PCR assay enabled accurate, noninvasive detection of GC, particularly at early stages, and may facilitate timely diagnosis and curative treatment.
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