Evidence map›Paper›PMID 40542787›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2025

Methylation of Tumor Suppressor Genes on Chromosome 9: Diagnostic Insights from a Nasopharyngeal Carcinoma in Vietnam.

Hue Hong Thieu, Thuy Ai Huyen Le, Thuan Duc Lao

Abstract read
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Article in Asian Pacific journal of cancer prevention : APJCP, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Epigenomic landscape of nasopharyngeal carcinoma.Medical oncology (Northwood, London, England) · 2025
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4 · The record

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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

3 authors.

Hue Hong ThieuThuan Duc Lao, Center for Life Science Research, Ho Chi Minh City Open University, Ho Chi Minh City, Vietnam.ORCID 0000-0002-8147-339X
Thuy Ai Huyen LeThuan Duc Lao, Center for Life Science Research, Ho Chi Minh City Open University, Ho Chi Minh City, Vietnam.ORCID 0000-0002-4825-3299
Thuan Duc LaoThuan Duc Lao, Center for Life Science Research, Ho Chi Minh City Open University, Ho Chi Minh City, Vietnam.ORCID 0000-0002-6459-3058

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMethylation represents the second hit in tumor development. In nasopharyngeal carcinoma (NPC), multiple tumor suppressor genes located on chromosome 9 under methylation.

aimsThis first case-control study aims to explore the methylation characteristics of DAPK, p16INK4α, p15INK4α, and p14ARF, individually and in combination, to evaluate their potential as promising biomarkers for nasopharyngeal carcinoma (NPC). MATERIALS AND

methodsA total of 70 NPC biopsy samples and 60 non-cancerous swab samples were enrolled into the current study. Genomic DNA extraction, bisulfite modification, and methylation-specific PCR (MSP) were used to analyze methylation status. Statistical analyses, including odds ratio (OR) calculations and methylation index (MI) evaluation, were conducted to determine the association between methylation and nasopharyngeal carcinoma (NPC).

resultsPromoter hypermethylation was observed in 75.71%, 78.57%, 52.86%, and 87.14% of samples for DAPK, p16INK4α, p15INK4α, and p14ARF, respectively. A significant association between the methylation status of these candidate genes and nasopharyngeal carcinoma (NPC) was identified. The methylation of these genes significantly increased the risk of NPC compared to control samples (OR > 1). Based on the methylation index (MI), 100% of NPC samples showed methylation in at least one gene (MI ≥ 0.25). An MI ≥ 0.25 demonstrated a sensitivity of 100% and a specificity of 50%, highlighting its potential as a diagnostic marker.

conclusionThis study highlights the potential of DAPK, p16INK4α, p15INK4α, and p14ARF methylation as biomarkers for the diagnosis and early screening of nasopharyngeal carcinoma (NPC) in Vietnamese patients. The findings support the use of a composite methylation index as a sensitive biomarker for the early detection and screening of NPC.

Indexed as

Biomarkers, TumorChromosomes, Human, Pair 9DNA MethylationGenes, Tumor SuppressorNasopharyngeal NeoplasmsAdultCarcinomaCase-Control StudiesCyclin-Dependent Kinase Inhibitor p16Death-Associated Protein KinasesFemaleFollow-Up StudiesHumansMaleMiddle AgedNasopharyngeal CarcinomaBiomarkers, TumorCyclin-Dependent Kinase Inhibitor p16Death-Associated Protein KinasesTumor Suppressor Protein p14ARFDAPKDiagnosisearly screeningINK4αmethylation

Identifiers

PMID40542787
PMCPMC12374528

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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.