Evidence map›Paper›PMID 41845480›Full record

ArticleClinical epigenetics2026

Effectiveness analysis and clinical application potential exploration of combined detection of PAX1/JAM3 gene methylation in early diagnosis of cervical precancerous lesions.

Guo Fan, Yu Xiaolu, Yiliminuer Keremu, Kong Weina, Xu Xiaohui, Ma Xiumin

Abstract read
In one paragraph

Article in Clinical epigenetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

What it found

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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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Guo Fan *Department of Medical Laboratory Center, Tumor Hospital Affiliated to Xinjiang Medical University, Xinjiang Key Laboratory of Molecular Biology for Endemic Diseases, No 789 Suzhou Road, Urumqi, 830011, Xinjiang, People's Republic of China.
Yu Xiaolu *Department of Medical Laboratory Center, Tumor Hospital Affiliated to Xinjiang Medical University, Xinjiang Key Laboratory of Molecular Biology for Endemic Diseases, No 789 Suzhou Road, Urumqi, 830011, Xinjiang, People's Republic of China.
Yiliminuer KeremuDepartment of Medical Laboratory Center, Tumor Hospital Affiliated to Xinjiang Medical University, Xinjiang Key Laboratory of Molecular Biology for Endemic Diseases, No 789 Suzhou Road, Urumqi, 830011, Xinjiang, People's Republic of China.
Kong WeinaDepartment of Medical Laboratory Center, Tumor Hospital Affiliated to Xinjiang Medical University, Xinjiang Key Laboratory of Molecular Biology for Endemic Diseases, No 789 Suzhou Road, Urumqi, 830011, Xinjiang, People's Republic of China.
Xu XiaohuiDepartment of Medical Laboratory Center, Tumor Hospital Affiliated to Xinjiang Medical University, Xinjiang Key Laboratory of Molecular Biology for Endemic Diseases, No 789 Suzhou Road, Urumqi, 830011, Xinjiang, People's Republic of China.
Ma XiuminDepartment of Medical Laboratory Center, Tumor Hospital Affiliated to Xinjiang Medical University, Xinjiang Key Laboratory of Molecular Biology for Endemic Diseases, No 789 Suzhou Road, Urumqi, 830011, Xinjiang, People's Republic of China. maxiumin1210@sohu.com.

Funding

the special scientific research project of young medical scientific and technological talents of Xinjiang Uygur Autonomous region Health and Family Planning Commission WJWY-202403the Xinjiang Key Laboratory of Molecular Biology for Endemic Diseases XJDFB2024G03
6 · The paper itself

Abstract

backgroundThe early and accurate diagnosis of cervical precancerous lesions is essential for mitigating the risk of cervical cancer. Given the limitations of traditional screening methods, such as inadequate sensitivity and low specificity, this study aims to assess the diagnostic performance of combined PAX1/JAM3 gene methylation testing for cervical intraepithelial neoplasia (CIN) and to explore its potential in triage management. Methylation testing serves as a tool for investigating the epigenetic alterations associated with diseases like cancer, thereby providing molecular biological evidence for diagnosis and prognosis.

methodsThis study included 431 cervical exfoliated cell samples, which consisted of CIN1, CIN2/3, cervical cancer (CC), and control groups. The methylation levels of the PAX1/JAM3 genes were assessed using quantitative methylation-specific PCR. The diagnostic efficacy of these genes for high-grade lesions (CIN2+) was analyzed through receiver operating characteristic (ROC) curve analysis and was compared with HPV testing and cytological examination. Additionally, the diagnostic performance of PAX1/SOX1 methylation was preliminarily evaluated in a sub-cohort of 100 cases. Further evaluation was conducted on the triage referral rate and the impact of clinical intervention using this biomarker in HPV-positive patients.

resultsThe area under the curve (AUC) for the PAX1/JAM3 methylation test in diagnosing CIN2+ was 0.89 (95% CI: 0.85-0.92), with a sensitivity of 83.1% and a specificity of 88.8%. In the sub-cohort, the PAX1/SOX1 combination also demonstrated high diagnostic potential for CIN3+ (AUC = 0.91), serving as a validation of methylation testing efficacy. In non-HPV16/18 positive patients, the sensitivity and specificity of methylation testing for CIN2+ were superior to those of cytology. Among patients undergoing colposcopy, 265 cases had results of ≤ASCUS, of which 51 were methylation positive, resulting in a colposcopy referral rate of 19.3%.

conclusionPAX1/JAM3 gene methylation testing demonstrates strong diagnostic efficacy for cervical precancerous lesions and holds significant potential in triage diagnosis. The PAX1/SOX1 panel also shows promise as a complementary biomarker.

Indexed as

Cell Adhesion MoleculesDNA MethylationEarly Detection of CancerPaired Box Transcription FactorsPrecancerous ConditionsUterine Cervical DysplasiaUterine Cervical NeoplasmsAdultBiomarkers, TumorFemaleHumansKruppel-Like Transcription FactorsMiddle AgedROC CurveSensitivity and SpecificitySOXB1 Transcription FactorsBiomarkers, TumorCell Adhesion MoleculesKruppel-Like Transcription FactorsPaired Box Transcription FactorsPAX1 transcription factorSOX1 protein, humanSOXB1 Transcription FactorsZNF582 protein, humanCervical intraepithelial neoplasiaDNA methylationJAM3Molecular Diagnostic TechniquesPAX1

Identifiers

PMID41845480
PMCPMC13107586

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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.