Evidence map›Paper›PMID 42763290›Full record

ArticleZhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences2026

[NPLOC4 promotes proliferation, invasion, and migration of hepatocellular carcinoma cells via enhancing Wnt/

Shuai Liang, Zichuan Lu, Zhongcheng Zhu, Tiantian Tang, Ke Ye

Abstract readEnglish Abstract
In one paragraph

Article in Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences, 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

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Shuai LiangDepartment of Biliary and Pancreatic Surgery, Xiangya Hospital, Central South University, Changsha 410008. doctorbach@csu.edu.cn.
Zichuan LuDepartment of Hepatology, Xiangya Hospital, Central South University, Changsha 410008.
Zhongcheng ZhuDepartment of Biliary and Pancreatic Surgery, Xiangya Hospital, Central South University, Changsha 410008.
Tiantian TangDepartment of Oncology, Fuyuan Campus, Xiangya Boai Rehabilitation Hospital, Changsha 410199, China.
Ke YeDepartment of Hepatology, Xiangya Hospital, Central South University, Changsha 410008. 404479@csu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesDysregulation of mitophagy contributes to the initiation and progression of hepatocellular carcinoma (HCC). Nuclear protein localization 4 homolog (NPLOC4) is an essential protein involved in various cellular processes and has been implicated in multiple cancers. Recent studies have suggested that NPLOC4 participates in the regulation of mitophagy; however, its role in HCC remains unclear. This study aims to investigate the role of NPLOC4 in mitophagy and its underlying regulatory mechanisms in HCC.

methodsRNA sequencing data from the GSE277232 and GSE251942 datasets obtained from the Gene Expression Omnibus (GEO) database were analyzed together with mitophagy-related genes collected from the GeneCards database to identify differentially expressed mitophagy-related genes in HCC. NPLOC4 expression was further analyzed and validated by Western blotting. Small interfering RNA (siRNA)-mediated knockdown of

resultsBioinformatics analysis identified

conclusionsNPLOC4 is highly expressed in HCC. Downregulation of NPLOC4 inhibits activation of the Wnt/β-catenin signaling pathway, thereby inhibiting mitophagy and ultimately inhibiting HCC cell proliferation, migration, and invasion. These findings suggest that NPLOC4 may serve as a potential biomarker and therapeutic target for HCC.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsMitophagyWnt Signaling Pathwaybeta CateninCell Line, TumorCell MovementCell ProliferationGene Expression Regulation, NeoplasticHumansNeoplasm InvasivenessRNA, Small Interferingbeta CateninRNA, Small Interferinghepatocellular carcinomainvasionmigrationmitophagyNPLOC4proliferation

Identifiers

PMID42763290
PMCPMC13589775

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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.