Journal article
Whole-genome methylation profiling of extracellular vesicle DNA in gastric cancer identifies intercellular communication features
- Abstract:
- Abstract Extracellular vesicles (EVs) are promising biomarkers for cancer diagnosis and prognosis due to their ability to carry specific biomolecular cargo, including DNA. However, the clinical utility of DNA methylation-based liquid biopsies using EV-DNA remains underexplored. The low quantity and relatively long length of EV-DNA complicate whole-genome methylation profiling. To address this, we develop Tn5-assisted Enzymatic Methyl-sequencing with Post-conversion Tailing (TEMPT), a bisulfite-free whole-genome profiling method for EV-DNA. TEMPT employs single-adapter Tn5 tagmentation, enzymatic conversion of unmodified cytosines, and post-conversion tailing to generate high-depth whole-genome EV-DNA methylomes. We apply TEMPT to EV-DNA from 58 gastric cancer and polyp samples, generating methylomes from sub-nanogram inputs and identifying differentially methylated regions (DMRs) that distinguish cancer from controls. We identify potential cancer biomarkers through DMR-associated genes, highlighting the roles of EVs in cellular communication. Our findings suggest that immune cells may serve as an alternative source of EV-DNA. This approach holds significant promise for advancing EV-DNA research and its applications in early disease diagnosis
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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(Preview, Version of record, pdf, 960.0KB, Terms of use)
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- Publisher copy:
- 10.1038/s41467-025-63435-w
Authors
- Publisher:
- Nature Research
- Journal:
- Nature Communications More from this journal
- Volume:
- 16
- Issue:
- 1
- Pages:
- 8084-8084
- Article number:
- 8084
- Publication date:
- 2025-08-29
- DOI:
- EISSN:
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2041-1723
- ISSN:
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2041-1723
- Language:
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English
- Keywords:
- Pubs id:
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2308678
- UUID:
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uuid_52ee1b79-8721-48c7-9db0-ac11def68d9c
- Local pid:
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pubs:2308678
- Source identifiers:
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W4413808643
- Deposit date:
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2025-11-06
- ARK identifier:
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- Copyright date:
- 2025
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