Evidence mapPaperPMID 40936767Full record

ArticlePeerJ2025

Development of a prognostic RiskScore model using efferocytosis-related signature genes for lung adenocarcinoma.

Zengmin Dai, Shaofeng Jin, Shanshan Huang, Bingyang Liu, Xingkai Shen, Yuhong Jin

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Article in PeerJ, 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

6 authors.

Zengmin DaiDepartment of Critical Care Medicine, Ningbo Medical Center Lihuili Hospital (The Affiliated Lihuili Hospital of Ningbo University), Ningbo, China.
Shaofeng JinDepartment of Critical Care Medicine, Ningbo Medical Center Lihuili Hospital (The Affiliated Lihuili Hospital of Ningbo University), Ningbo, China.
Shanshan HuangDepartment of Critical Care Medicine, Ningbo Medical Center Lihuili Hospital (The Affiliated Lihuili Hospital of Ningbo University), Ningbo, China.
Bingyang LiuDepartment of Critical Care Medicine, Ningbo Medical Center Lihuili Hospital (The Affiliated Lihuili Hospital of Ningbo University), Ningbo, China.
Xingkai ShenDepartment of Critical Care Medicine, Ningbo Medical Center Lihuili Hospital (The Affiliated Lihuili Hospital of Ningbo University), Ningbo, China.
Yuhong JinDepartment of Critical Care Medicine, Ningbo Medical Center Lihuili Hospital (The Affiliated Lihuili Hospital of Ningbo University), Ningbo, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Lung adenocarcinoma (LUAD) has high incidence and mortality rates. Efferocytosis is involved in the progression of various cancers. The current work set out to develop a prognosis signature using efferocytosis-related genes (ERGs) for LUAD. Methods: Public databases were accessed to obtain bulk and single-cell data of LUAD. Molecular subtyping of LUAD was performed using ConsensusClusterPlus, and efferocytosis-related candidate genes were screened by weighted gene co-expression network analysis (WGCNA) in combination with differential analysis. Subsequently, Least Absolute Shrinkage and Selection Operator (LASSO) regression was applied to construct a prognostic RiskScore model, followed by evaluating the relationship between the RiskScore, immune infiltration, and drug sensitivity. Single-cell transcriptomic profiling of LUAD was performed with the Seurat package to elucidate the cellular origins of the key genes. The expression and potential function of the representative genes were verified by reverse transcriptional quantitative polymerase chain reaction (qPCR) (RT-qPCR), Cell Counting Kit-8 (CCK-8), wound healing, and Transwell assays. Results: Two molecular subtypes of LUAD with different outcomes and clinical features were identified. Candidate ERGs were mainly enriched in inflammatory and immune-related pathways. Subsequently, seven key genes ( Conclusions: Our results provided novel insights for the prognosis prediction and personalized treatment of LUAD.

Indexed as

Adenocarcinoma of LungLung NeoplasmsPhagocytosisBiomarkers, TumorEfferocytosisGene Expression ProfilingGene Expression Regulation, NeoplasticHumansPrognosisTranscriptomeBiomarkers, TumorDrug sensitivityEfferocytosisImmune infiltrationLung adenocarcinomaPrognostic signatureRiskScore model

Identifiers

PMID40936767
PMCPMC12422274

What Socratic holds

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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 Socratic graph.