Evidence map›Paper›PMID 40123906›Full record

ArticleFrontiers in oncology2025

GINS1 is a prognostic biomarker and correlated with methylation and immune escape in liver hepatocellular carcinoma.

Mingchao Liang, Tianqi Lai, Zhen Li, Wei Yu, Mingrong Cao, Nan Yao, Youzhu Hu, Tongzheng Liu, Junjie Liang

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Article in Frontiers in oncology, 2025. 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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5 · Who and what money

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9 authors.

Mingchao Liang *Department of General Surgery, The Affiliated Shunde Hospital, Jinan University, Foshan, China.
Tianqi Lai *Department of Hepatobiliary Surgery, The First Affiliated Hospital, Jinan University, Guangzhou, China.
Zhen Li *Department of General Surgery, The Affiliated Shunde Hospital, Jinan University, Foshan, China.
Wei YuDepartment of Hepatobiliary Surgery, The First Affiliated Hospital, Jinan University, Guangzhou, China.
Mingrong CaoDepartment of Hepatobiliary Surgery, The First Affiliated Hospital, Jinan University, Guangzhou, China.
Nan YaoDepartment of Pathophysiology, Medical College, Jinan University, Guangzhou, China.
Youzhu HuDepartment of General Surgery, The Affiliated Shunde Hospital, Jinan University, Foshan, China.
Tongzheng LiuGuangdong Province Key Laboratory of Pharmacodynamic Constituents of Traditional Chinese Medicine and New Drugs Research, College of Pharmacy, Jinan University, Guangzhou, China.
Junjie LiangDepartment of Hepatobiliary Surgery, The First Affiliated Hospital, Jinan University, Guangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

GINS1 is correlated with a poor prognosis in numerous cancers including liver hepatocellular carcinoma (LIHC). Here, efforts have been made to explore the function and underlying mechanism in LIHC through bioinformatics analysis. The mRNA and protein expression data of GINS1 were downloaded from The Cancer Genome Atlas (TCGA) database, the Clinical Proteomic Tumor Analysis Consortium (CPTAC), the University of Alabama at Birmingham CANcer Data Analysis Portal (UALCAN), and the Human Protein Atlas (HPA) database. Moreover, the protein expression of GINS1 was further substantiated by immunohistochemistry staining from 116 clinical samples. Subsequently, the diagnostic and prognostic role of GINS1 in LIHC patients were determined using receiver operating characteristic (ROC) analysis and the Kaplan-Meier plotter (KM-plotter) database. GeneMANIA and STRING databases were respectively used to construct gene and protein-protein interaction (PPI) networks of GINS1. Enrichment analyses were conducted to investigate the functions of GINS1. To assess the genetic alterations, methylation, and prognostic value, cBioPortal, and MethSurv databases were utilized. Additionally, Tumor Immune Estimation Resource (TIMER), Tumor-Immune System Interaction Database (TISIDB), and Gene Expression Profiling Interactive Analysis (GEPIA) were used to explore the correlation with tumor immune. Differential expression analyses validated the upregulation of GINS1 in LIHC. Furthermore, the prognostic and diagnostic values of GINS1 were substantiated by the ROC curve, Kaplan-Meier plotters, and forest plots. Further enrichment, methylation, and tumor immune microenvironment analyses showed an intimate connection with GINS1. In conclusion, GINS1 which is correlated with methylation and immune escape may predict the prognosis of LIHC.

Indexed as

biomarkersGINS1immune escapeliver hepatocellular carcinomamethylationprognosis

Identifiers

PMID40123906
PMCPMC11925790

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