Evidence map›Paper›PMID 42018581›Full record

ArticlePloS one2026

The role of SPP1 in evaluating the prognosis, immune infiltration, and drug sensitivity of hepatocellular carcinoma.

Kai Cui, Xia Li, Yongrun Li, Zhong Li, Du Wang, Xinhong Wang, Shuxin Qin, Junjie Li, Jiaye Long

Abstract read
In one paragraph

Article in PloS one, 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

What it found

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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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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

9 authors.

Kai CuiDepartment of Interventional Radiology, Inner Mongolia Forestry General Hospital, The Second Clinical Medical School of Inner Mongolia Minzu University, Yakeshi, Inner Mongolia, China.
Xia LiDepartment of Interventional Radiology, Inner Mongolia Forestry General Hospital, The Second Clinical Medical School of Inner Mongolia Minzu University, Yakeshi, Inner Mongolia, China.
Yongrun LiDepartment of Interventional Radiology, Xinhui Hospital Affiliated to Southern Medical University, Xinhui District People's Hospital, Jiangmen, Guangdong, China.
Zhong LiDepartment of Medical Imaging, Inner Mongolia Forestry General Hospital, The Second Clinical Medical School of Inner Mongolia Minzu University, Yakeshi, Inner Mongolia, China.
Du WangDepartment of Interventional Radiology, Inner Mongolia Forestry General Hospital, The Second Clinical Medical School of Inner Mongolia Minzu University, Yakeshi, Inner Mongolia, China.
Xinhong WangDepartment of Interventional Radiology, Inner Mongolia Forestry General Hospital, The Second Clinical Medical School of Inner Mongolia Minzu University, Yakeshi, Inner Mongolia, China.
Shuxin QinDepartment of Interventional Radiology, Inner Mongolia Forestry General Hospital, The Second Clinical Medical School of Inner Mongolia Minzu University, Yakeshi, Inner Mongolia, China.
Junjie LiDepartment of Interventional Radiology, Inner Mongolia Forestry General Hospital, The Second Clinical Medical School of Inner Mongolia Minzu University, Yakeshi, Inner Mongolia, China.
Jiaye LongDepartment of Interventional Radiology, Xinhui Hospital Affiliated to Southern Medical University, Xinhui District People's Hospital, Jiangmen, Guangdong, China.ORCID https://orcid.org/0000-0003-2821-4011

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSecretory phosphoprotein 1 (SPP1) has been linked to tumor progression and immune regulation, but its prognostic value, impact on the tumor immune microenvironment (TIME), and drug sensitivity in HCC remain unclear.

methodsWe performed a pan-cancer analysis using TIMER and validated SPP1 upregulation in six GEO datasets (GSE45436, GSE54236, GSE121248, GSE76427, GSE64041, and GSE60502) and HPA protein data. In TCGA-LIHC, we assessed overall survival (OS) and progression-free survival (PFS) using univariate/multivariate Cox analyses, ROC analysis, and a calibrated nomogram. We identified differentially expressed genes (DEGs) and performed GO/KEGG and GSEA analyses. Immune infiltration was estimated with CIBERSORT and TIMER, and relationships with immune checkpoints were explored. Drug sensitivity was predicted with pRRophetic using GDSC data. In vitro, SPP1 was knocked down or overexpressed in HCC cell lines to evaluate effects on proliferation, migration, invasion, and apoptosis via qRT-PCR, Western blot, CCK-8, colony formation, wound healing, Transwell invasion, and TUNEL assays.

resultsSPP1 was significantly upregulated in HCC at mRNA and protein levels. High SPP1 predicted poorer OS and PFS and was associated with higher histological grade, advanced stage, and greater T stage. The nomogram showed good calibration and discrimination. DEGs and enrichment analyses implicated cytokine receptor interaction, fatty acid metabolism, and PI3K-Akt signaling; GSEA confirmed immune- and metabolism-related pathways. High SPP1 correlated with higher immune/ESTIMATE scores, increased M0/M2 macrophages and dendritic cells, reduced CD8 + T cells, and upregulation of multiple immune checkpoints. Drug-sensitivity predictions showed high-SPP1 tumors were more sensitive to several anti-cancer drugs (e.g., sorafenib), while resistance to others was suggested. Functionally, SPP1 knockdown inhibited, while overexpression promoted, proliferation, migration, and invasion; knockdown increased apoptosis.

conclusionsSPP1 acts as an oncogenic driver in HCC, associated with poor prognosis, an immunosuppressive TIME, and distinct drug-response patterns.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsOsteopontinApoptosisCell Line, TumorCell MovementCell ProliferationDrug Resistance, NeoplasmGene Expression Regulation, NeoplasticHumansPrognosisTumor MicroenvironmentOsteopontinSPP1 protein, human

Identifiers

PMID42018581
PMCPMC13102187

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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.