Evidence map›Paper›PMID 42564509›Full record

ArticleHepatology forum2026

High expression of USP15 affects tumor progression and immune infiltration in hepatocellular carcinoma.

Si-Peng Wu, Xue-Yuan Zhang, Hui-Dan Chen, Fu-Zhi Jin, Nan Jiang, Jia-Xing Zhang, Zhe-Long Liang

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Article in Hepatology forum, 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

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Si-Peng WuMedical College of Yanbian University, Jilin, China.
Xue-Yuan ZhangMedical College of Yanbian University, Jilin, China.
Hui-Dan ChenMedical College of Yanbian University, Jilin, China.
Fu-Zhi JinDepartment of Anesthesia, Hospital of Yanbian University, Jilin, China.
Nan JiangMedical College of Yanbian University, Jilin, China.
Jia-Xing ZhangMedical College of Yanbian University, Jilin, China.
Zhe-Long LiangDepartment of Anesthesia, Hospital of Yanbian University, Jilin, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Aim: Ubiquitin-specific protease 15 (USP15) is closely associated with the occurrence and progression of hepatocellular carcinoma (HCC). However, its role in shaping the immune landscape of HCC remains unclear. Materials and Methods: The expression levels, proportions, and spatial distributions of USP15 and specific immune cell subsets in HCC tissues were evaluated using multiplex immunohistochemistry (mIHC). Results: In the tumor parenchyma of HCC tissues, the infiltration of immune cells, particularly natural killer (NK) cells, was significantly reduced (p<0.05). Further analyses revealed that USP15 expression levels were significantly associated with clinical stage and other clinicopathological parameters (p<0.05). In particular, NK cell infiltration was significantly correlated with N stage, M stage, and overall tumor-node-metastasis (TNM) stage (p<0.05). Conclusion: USP15 contributes to the establishment of an immunosuppressive tumor microenvironment in HCC by inhibiting T cell and NK cell infiltration, facilitating programmed death-ligand 1 (PD-L1)-mediated immune evasion, and enhancing macrophage recruitment. These findings indicate that USP15 may serve as a potential therapeutic target for HCC.

Indexed as

Hepatocellular carcinomaimmune cell infiltratestumor immune microenvironmentubiquitin-specific peptidase 15 (USP15)

Identifiers

PMID42564509
PMCPMC13442720

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