Evidence map›Paper›PMID 41859313›Full record

ArticleInternational journal of general medicine2026

Predicting the Impact of ARHGAP33 Gene on Liver Cancer Prognosis Based on Multi-Algorithm Model.

Yaohui Zhao, Chenjie Wang, Xiaotong Shen, Xinhui Cao, Zi Wang, Huijiao Jiang, Xueling Chen, Xiangwei Wu

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Article in International journal of general 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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1 · What the graph read from it

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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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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Yaohui Zhao *School of Medicine, Shihezi University, Shihezi, 832000, People's Republic of China.
Chenjie Wang *School of Medicine, Shihezi University, Shihezi, 832000, People's Republic of China.
Xiaotong ShenSchool of Medicine, Shihezi University, Shihezi, 832000, People's Republic of China.
Xinhui CaoSchool of Medicine, Shihezi University, Shihezi, 832000, People's Republic of China.
Zi WangSchool of Medicine, Shihezi University, Shihezi, 832000, People's Republic of China.
Huijiao JiangSchool of Medicine, Shihezi University, Shihezi, 832000, People's Republic of China.
Xueling ChenSchool of Medicine, Shihezi University, Shihezi, 832000, People's Republic of China.
Xiangwei WuSchool of Medicine, Shihezi University, Shihezi, 832000, People's Republic of China.ORCID 0009-0008-8884-8992

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To investigate the impact of Rho GTPase-activating protein 33 (ARHGAP33) and its synergistic interaction with SFPQ on the prognosis of hepatocellular carcinoma (HCC) through bioinformatics and experimental research. Materials and Methods: RNA sequencing data from The Cancer Genome Atlas (TCGA) were analyzed to assess ARHGAP33 expression in hepatocellular carcinoma (HCC). Co-expressed genes were identified using WGCNA and GSVA, and integrated into a multi-algorithm consensus prognostic model. Results: The analysis of the TCGA database indicated a marked overexpression of ARHGAP33 mRNA in tissues from hepatocellular carcinoma (LIHC), with a statistically significant finding (P < 0.001). WGCNA revealed that SFPQ is a gene associated with ARHGAP33. In the developed consensus prognostic model, survival analysis using Kaplan-Meier (K-M) alongside the CoxBoost model demonstrated that the overall survival time for patients classified as high-risk was significantly less than that of those classified as low-risk (P < 0.05).The Institutional Review Board at Shihezi University granted ethical approval for this research (Ethics Application No.: KJ2025-290-01). Conclusion: The expression level of ARHGAP33 affects HCC prognosis, and its synergistic overexpression with SFPQ impairs the prognosis of HCC patients. ARHGAP33 could potentially be used as a biomarker for evaluating prognosis in hepatocellular carcinoma (HCC), offering a new theoretical foundation for enhancing HCC outcomes.

Indexed as

ARHGAP33 genebioinformaticshepatocellular carcinomamulti-algorithmprognostic model

Identifiers

PMID41859313
PMCPMC12998573

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