Evidence map›Paper›PMID 42856638›Full record

ArticleLiver research (Beijing, China)2026

MND1 protein mediates DNA damage repair and is a promising novel therapeutic target in hepatocellular carcinoma.

Cheng Wang, Minghua Hu, Wanyu Xia, Qian Zheng, Chengfei Zhang, Ruoyu Shi, Chengsong Cao, Hongping Xia, Chengyun Yao

Abstract read
In one paragraph

Article in Liver research (Beijing, China), 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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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

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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

9 authors.

Cheng WangXuzhou Central Hospital & Zhongda Hospital & Jiangsu Provincial Key Laboratory of Critical Care Medicine & Institute for Advanced Study of Life and Health, School of Medicine, Southeast University, Nanjing, Jiangsu, China.
Minghua HuDepartment of Surgery, The First Affiliated Hospital of Wannan Medical University (Yijishan Hospital), Wuhu, Anhui, China.
Wanyu XiaXuzhou Central Hospital & Zhongda Hospital & Jiangsu Provincial Key Laboratory of Critical Care Medicine & Institute for Advanced Study of Life and Health, School of Medicine, Southeast University, Nanjing, Jiangsu, China.
Qian ZhengDepartment of Pathology, Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School, Nanjing, Jiangsu, China.
Chengfei ZhangDepartment of General Surgery, Sir Run Run Hospital, Nanjing Medical University, Nanjing, Jiangsu, China.
Ruoyu ShiDepartment of Pathology, National University Hospital, National University Health System, Singapore.
Chengsong CaoXuzhou Central Hospital & Zhongda Hospital & Jiangsu Provincial Key Laboratory of Critical Care Medicine & Institute for Advanced Study of Life and Health, School of Medicine, Southeast University, Nanjing, Jiangsu, China.
Hongping XiaXuzhou Central Hospital & Zhongda Hospital & Jiangsu Provincial Key Laboratory of Critical Care Medicine & Institute for Advanced Study of Life and Health, School of Medicine, Southeast University, Nanjing, Jiangsu, China.
Chengyun YaoJiangsu Cancer Hospital, The Affiliated Cancer Hospital of Nanjing Medical University, Jiangsu Institute of Cancer Research, Nanjing, Jiangsu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and aims: Hepatocellular carcinoma (HCC) remains a leading cause of cancer-related mortality worldwide, highlighting the urgent need to identify novel therapeutic targets. Bioinformatic analysis initially identified meiotic nuclear division 1 ( Methods: The expression profile of MND1 was validated using data from public databases along with 22 paired clinical HCC specimens. The functional roles of MND1 were investigated through Results: Multi-omics analysis and clinical validation revealed that MND1 is overexpressed in HCC tissues and significantly correlates with poor prognosis. Comprehensive Conclusions: These findings suggest that MND1 may serve as both a potential molecular marker and an oncogenic contributor in HCC. Importantly, the newly identified MND1-TRIM28-DDR regulatory axis offers a promising rationale for the development of targeted therapeutic strategies.

Indexed as

DNA damage repairHepatocellular carcinoma (HCC)Meiotic nuclear division 1 (MND1)Therapeutic targetTripartite motif-containing 28 (TRIM28)

Identifiers

PMID42856638
PMCPMC13649621

What OpenQuestion holds

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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.