Evidence map›Paper›PMID 40770743›Full record

ArticleEuropean journal of medical research2025

Development of a PPP1R14B-associated immune prognostic model for hepatocellular carcinoma.

Ligang Zhao, Xiaoling Jin, Qiushi Yu, Yigang He, Facai Yang, Weihu Ma, Zhengqing Lei, Jiahua Zhou

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Article in European journal of medical research, 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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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

8 authors.

Ligang ZhaoHepato-Pancreato-Biliary Center, Zhongda Hospital, School of Medicine, Southeast University, Nanjing, China.
Xiaoling JinHepato-Pancreato-Biliary Center, Zhongda Hospital, School of Medicine, Southeast University, Nanjing, China.
Qiushi YuHepato-Pancreato-Biliary Center, Zhongda Hospital, School of Medicine, Southeast University, Nanjing, China.
Yigang HeHepato-Pancreato-Biliary Center, Zhongda Hospital, School of Medicine, Southeast University, Nanjing, China.
Facai YangHepato-Pancreato-Biliary Center, Zhongda Hospital, School of Medicine, Southeast University, Nanjing, China.
Weihu MaHepato-Pancreato-Biliary Center, Zhongda Hospital, School of Medicine, Southeast University, Nanjing, China.
Zhengqing LeiHepato-Pancreato-Biliary Center, Zhongda Hospital, School of Medicine, Southeast University, Nanjing, China.
Jiahua ZhouHepato-Pancreato-Biliary Center, Zhongda Hospital, School of Medicine, Southeast University, Nanjing, China. zhoujh@seu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis study sought to comprehensively examine PPP1R14B's function and its immune-related correlations in hepatocellular carcinoma (HCC).

methodsRNA-seq and clinical information for HCC were procured from TCGA database. The links between PPP1R14B level and immune modulators plus immune cell populations were examined through Spearman correlation assessment. The immune landscape was assessed utilizing CIBERSORT and ESTIMATE algorithms. Gene set variation examination helped explore immune cell populations and their activities. The construction of prognostic models involved univariate and multivariate Cox regression investigations. Immunotherapy response and drug sensitivity were evaluated based on tumor immune dysfunction and exclusion (TIDE) and genomics of drug sensitivity in cancer (GDSC), respectively.

resultsPPP1R14B levels were substantially elevated in HCC specimens versus normal tissues, and elevated expression independently linked to diminished survival rates. PPP1R14B levels exhibited notable associations with various immune cells, including memory B lymphocytes, M1/M2 macrophage populations, CD8-positive T lymphocytes, and T follicular helper cells. The analysis revealed distinct variations in immune scores and multiple immune cell enrichment patterns between elevated and reduced PPP1R14B expression categories, suggesting immune status connections. Elevated PPP1R14B cohorts demonstrated increased TIDE scores, alongside decreased IC50 measurements for specific drugs, including temsirolimus, sorafenib, rapamycin, dasatinib, and cytarabine, pointing to treatment response relationships. The study constructed a PPP1R14B-linked immune prediction model, demonstrating acceptable prognostic capability for HCC patients. The incorporation of pathological grade and pathological T stage parameters alongside risk scores in a nomogram enhanced the predictive accuracy.

conclusionsThis investigation thoroughly uncovered the significance of PPP1R14B in HCC, and established a PPP1R14B-linked immune prognostic signature. The findings facilitate the classification of HCC patients into distinct cohorts for developing individualized therapeutic approaches.

Indexed as

Biomarkers, TumorCarcinoma, HepatocellularLiver NeoplasmsProtein Phosphatase 1Gene Expression Regulation, NeoplasticHumansMalePrognosisBiomarkers, TumorProtein Phosphatase 1Hepatocellular carcinomaImmune statusPPP1R14BPrognosis

Identifiers

PMID40770743
PMCPMC12326615

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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.