Evidence map›Paper›PMID 42169100›Full record

ArticleBMC medicine2026

γH2AX and p53 Immunohistochemistry predict the incidence risk of esophageal squamous precancerous lesions.

Xiangwen Cheng, Ying Liu, Huanyu Chen, Yaqi Pan, Zhe Hu, Zhen Liu, Fangfang Liu, Wenlei Yang, Chuanhai Guo, Lixin Zhang and 9 more

Abstract read
In one paragraph

Article in BMC medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

19 authors.

Xiangwen Cheng *Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Genetics, Peking University Cancer Hospital & Institute, Beijing, China.
Ying Liu *Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Genetics, Peking University Cancer Hospital & Institute, Beijing, China.
Huanyu Chen *Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Genetics, Peking University Cancer Hospital & Institute, Beijing, China.
Yaqi PanKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Genetics, Peking University Cancer Hospital & Institute, Beijing, China.
Zhe HuKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Genetics, Peking University Cancer Hospital & Institute, Beijing, China.
Zhen LiuKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Genetics, Peking University Cancer Hospital & Institute, Beijing, China.
Fangfang LiuKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Genetics, Peking University Cancer Hospital & Institute, Beijing, China.
Wenlei YangKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Genetics, Peking University Cancer Hospital & Institute, Beijing, China.
Chuanhai GuoKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Genetics, Peking University Cancer Hospital & Institute, Beijing, China.
Lixin ZhangAnyang Cancer Hospital, Anyang, China.
Liheng ZhangAnyang Cancer Hospital, Anyang, China.
Fenglei LiHua County People's Hospital, Hua County, Anyang, China.
Jiangang LiHua County People's Hospital, Hua County, Anyang, China.
Xinna LiuHealth Commission of Hua County, Anyang, China.
Haijun YangDepartment of Pathology, Anyang Cancer Hospital, Anyang, China.
Muyan CaiDepartment of Pathology, State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center for Cancer, Sun Yat-sen University Cancer Center, Guangzhou, 510060, China. caimy@sysucc.org.cn.
Mengfei LiuKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Department of Genetics, Peking University Cancer Hospital & Institute, Beijing, China.
Zhonghu HeState Key Laboratory of Molecular Oncology, Beijing Key Laboratory of Carcinogenesis and Translational Research, Department of Genetics, Peking University Cancer Hospital & Institute, No.52 Fucheng Road, Haidian District, Beijing, 100142, China. zhonghuhe@foxmail.com.
Yang KeState Key Laboratory of Molecular Oncology, Beijing Key Laboratory of Carcinogenesis and Translational Research, Department of Genetics, Peking University Cancer Hospital & Institute, No.52 Fucheng Road, Haidian District, Beijing, 100142, China. keyang@bjmu.edu.cn.

Funding

Key R&D Program of Ningxia Hui Autonomous Region 2025BEG01011Science and Technology Plan of Tibet Autonomous Region XZ202501JD0021
6 · The paper itself

Abstract

backgroundCurrent screening practices for esophageal squamous cell carcinoma (ESCC) subject to both over- and under-surveillance of precancerous lesions. This study aims to evaluate potential immunohistochemical (IHC) markers associated with the incidence of ESCC and to establish an IHC-based panel for surveillance.

methodsTissue microarrays were constructed using 946 formalin-fixed, paraffin-embedded (FFPE) samples from 883 participants with baseline Lugol-unstained lesions (LULs) enrolled in a population-based screening trial. Candidate IHC markers were identified from literature and our previous findings. IHC results (H-scores) were quantified via HALO software, and optimal cut-offs were set by X-tile. Incident esophageal malignancy identified during a median follow-up of 11.76 years served as the outcome. Cox regression models were applied to identify predictive markers.

resultsEight candidate markers were evaluated. After multivariable adjustment and backward elimination, γH2AX and p53 were identified as significant predictors [HR (95% CI)

conclusionsγH2AX, a novel incidence-warning IHC marker for esophageal squamous precancerous lesions, combined with p53, showed robust and durable predictive performance for incident malignancy after one-time screening. Integrating IHC testing could help refine risk stratification and mitigate over- and under-surveillance within current ESCC screening protocol.

Indexed as

Biomarkers, TumorEsophageal NeoplasmsEsophageal Squamous Cell CarcinomaHistonesPrecancerous ConditionsTumor Suppressor Protein p53AgedFemaleHumansImmunohistochemistryIncidenceMaleMiddle AgedBiomarkers, TumorH2AX protein, humanHistonesTP53 protein, humanTumor Suppressor Protein p53Esophageal squamous cell carcinomaImmunohistochemical markersPrecancerous lesionsRisk stratificationSurveillance

Identifiers

PMID42169100
PMCPMC13371648

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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.