Evidence map›Paper›PMID 40582262›Full record

ArticleOral oncology2025

Optimization of methylation capture sequencing workflow in formalin fixed tissue from oral squamous cell carcinoma patients.

Minh Phuong Dong, Kesava Asam, Carissa M Thomas, Nicholas F Callahan, Paul C Walker, Khanh K Nguyen, Yi Ye, Ke Xu, Bradley E Aouizerat, Chi T Viet

Abstract readMulticenter Study
In one paragraph

Article in Oral oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Minh Phuong DongDepartment of Oral and Maxillofacial Surgery, School of Dentistry, Loma Linda University, Loma Linda, CA, the United States of America.
Kesava AsamTranslational Research Center, New York University College of Dentistry, New York, NY, the United States of America; Department of Oral and Maxillofacial Surgery, New York University College of Dentistry, New York, NY, the United States of America.
Carissa M ThomasDepartment of Otolaryngology, University of Alabama at Birmingham, Birmingham, AL, the United States of America; Department of Otolaryngology Head & Neck Surgery, University of Colorado, Aurora, CO, the United States of America.
Nicholas F CallahanDepartment of Oral and Maxillofacial Surgery, School of Dentistry, University of Illinois, Chicago, IL, the United States of America.
Paul C WalkerDepartment of Otolaryngology - Head & Neck Surgery, Loma Linda University Health, Loma Linda, CA, the United States of America.
Khanh K NguyenDepartment of Otolaryngology - Head & Neck Surgery, Loma Linda University Health, Loma Linda, CA, the United States of America.
Yi YeTranslational Research Center, New York University College of Dentistry, New York, NY, the United States of America; Department of Oral and Maxillofacial Surgery, New York University College of Dentistry, New York, NY, the United States of America; NYU Pain Research Center, Department of Molecular Pathobiology, New York University College of Dentistry, New York, NY, the United States of America.
Ke XuDepartment of Psychiatry, Yale School of Medicine, New Haven, CT, the United States of America; VA Connecticut Healthcare System, West Haven, CT, the United States of America.
Bradley E AouizeratTranslational Research Center, New York University College of Dentistry, New York, NY, the United States of America; Department of Oral and Maxillofacial Surgery, New York University College of Dentistry, New York, NY, the United States of America.
Chi T VietDepartment of Oral and Maxillofacial Surgery, School of Dentistry, Loma Linda University, Loma Linda, CA, the United States of America. Electronic address: cviet@llu.edu.

Funding

Targeting HB-EGF and trigeminal EGFR for oral cancer pain and opioid toleranceR01DE032501 · NIDCR · NEW YORK UNIVERSITY · PI YE, YI · 2022 to 2025
$4.0M
The REASON Score: An Epigenetic And Clinicopathologic Score to Predict Risk of Poor Survival in Early Stage Oral Squamous Cell Carcinoma PatientsR01DE031395 · NIDCR · LOMA LINDA UNIVERSITY · PI Chi T. Viet · 2022 to 2026
$3.7M
PROSPECT: Premalignant Oral Lesions Pathology and Epigenetic Risk Prediction ToolR01CA293995 · NCI · LOMA LINDA UNIVERSITY · PI AOUIZERAT, BRADLEY E, PEARSON, ALEXANDER THOMAS · 2024 to 2025
$1.4M
Clinical study to evaluate the methylation signature of head and neck squamous cell carcinoma painK23DE030250 · NIDCR · LOMA LINDA UNIVERSITY · PI VIET, CHI T. · 2021 to 2025
$865k
NCI NIH HHS R01 CA293995NIDCR NIH HHS K23 DE030250NIDCR NIH HHS R01 DE031395NIDCR NIH HHS R01 DE032501
6 · The paper itself

Abstract

backgroundOral squamous cell carcinoma (OSCC) is typically diagnosed at advanced stages, resulting in poor survival rates. Epigenetic alterations, especially DNA methylation, are important early and key contributors to OSCC pathogenesis, but comprehensive epigenetic analysis has traditionally been confounded by cancer tissue availability, with fresh-frozen tissues being the gold standard but difficult to obtain.

methodsThis study established and optimized a new workflow for the use of methylation capture sequencing (MC-seq) to analyze DNA methylation profiles in formalin-fixed paraffin-embedded (FFPE) tissues. Twelve OSCC patients were randomly selected from a prospective, multi-institutional study. Paired fresh-frozen and FFPE tissues were collected and processed for DNA extraction and MC-seq. Data were pre-processed using Bismark and methylKit pipelines. Methylation concordance between FFPE and fresh-frozen samples was assessed by comparing β-value correlation.

resultsDNA from FFPE and fresh-frozen OSCC samples showed minimal differences in fragmentation, with FFPE achieving high mapping efficiency (average 71.6%) and retaining an average of about 5 million CpG sites at 10× depth. The distributions of CpG in the methylome region, including promoter, exonic, intronic, and intergenic regions, showed similar patterns between sample types. Additionally, the methylation levels of all matched CpG sites in our 12-gene prognostic panel showed a strong correlation (r ≥ 0.97) between FFPE and fresh-frozen samples.

conclusionOur findings indicate that FFPE samples are reliable for methylation capture sequencing, offering a new, scalable and reliable alternative to fresh-frozen samples for large-scale OSCC research.

Indexed as

Carcinoma, Squamous CellDNA MethylationMouth NeoplasmsAgedFemaleFormaldehydeHumansMaleMiddle AgedParaffin EmbeddingProspective StudiesSequence Analysis, DNATissue FixationWorkflowFormaldehydeFFPEMC-seqMethylationOSCC

Identifiers

PMID40582262
PMCPMC13249506

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.