5-hydroxymethylcytosine signature in plasma extracellular vesicle DNA as a diagnostic molecular biomarker for precancerous lesions of gastric cancer

Haoyu Chen , Tianyu Gao , Hangyu Chen , Lei Zhang , Xianglong Chen , Maimaitiyasen Duolikun , Xiaxuan Li , Xuehui Li , Long Chen , Han Gao , Qi Li , Xinyu Hao , Pingping Zhou , Ningning Ren , Jian Lin , Yangang Wang

Extracellular Vesicles and Circulating Nucleic Acids ›› 2025, Vol. 6 ›› Issue (4) : 822 -42.

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Extracellular Vesicles and Circulating Nucleic Acids ›› 2025, Vol. 6 ›› Issue (4) :822 -42. DOI: 10.20517/evcna.2025.76
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5-hydroxymethylcytosine signature in plasma extracellular vesicle DNA as a diagnostic molecular biomarker for precancerous lesions of gastric cancer

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Abstract

Aim: Precancerous lesions of gastric cancer (PLGC) represent a critical window for prevention. Developing non-invasive tools that can reliably detect these lesions is therefore a prerequisite for lowering gastric-cancer incidence. Recent work has highlighted the diagnostic promise of plasma extracellular vesicle DNAs (evDNAs) and the 5-hydroxymethylcytosine (5hmC)-Seal epigenomic platform. Here we profiled genome-wide 5hmC patterns in circulating evDNA to discover biomarkers and build a classification model.

Methods: We performed whole-genome 5hmC-Seal on plasma evDNAs from 67 PLGC patients and 67 healthy individuals. By identifying trend-expressed differentially hydroxymethylated regions (DhMRs), we used machine learning algorithms to screen for diagnostic biomarkers of PLGC and established a corresponding diagnostic model.

Results: We ultimately constructed a diagnostic model comprising nine DhMRs. In the test set, the area under the curve (AUC) value was 0.963, with an accuracy of 0.886, sensitivity of 95.45%, and specificity of 81.82%. These results indicate that DhMRs in evDNA can serve as diagnostic biomarkers for PLGC, with good diagnostic capability and reliability. Correlation analysis showed a strong association between the DhMRs in the diagnostic model and clinical pathological indicators of PLGC.

Conclusion: We developed a non-invasive diagnostic model for PLGC by profiling 5hmC in plasma evDNA. In both accuracy and inter-batch robustness, it surpasses all previously reported assays. Our findings establish plasma-evDNA 5hmC profiling as a reliable, minimally invasive strategy for the early detection and precise diagnosis of gastric precancerous lesions, and provide a new translational and clinical framework for future work.

Keywords

Precancerous lesions of gastric cancer / 5-hydroxymethylcytosine / extracellular vesicle DNAs / molecular biomarker

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Haoyu Chen, Tianyu Gao, Hangyu Chen, Lei Zhang, Xianglong Chen, Maimaitiyasen Duolikun, Xiaxuan Li, Xuehui Li, Long Chen, Han Gao, Qi Li, Xinyu Hao, Pingping Zhou, Ningning Ren, Jian Lin, Yangang Wang. 5-hydroxymethylcytosine signature in plasma extracellular vesicle DNA as a diagnostic molecular biomarker for precancerous lesions of gastric cancer. Extracellular Vesicles and Circulating Nucleic Acids, 2025, 6(4): 822-42 DOI:10.20517/evcna.2025.76

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