Evidence map›Paper›PMID 40537732›Full record

ArticleDiscover oncology2025

PTX3 as a diagnostic and prognostic biomarker in lung adenocarcinoma: a comprehensive analysis.

Shaobo Zhou, Na Li, Dina Haishaer, Hongmei Zhao

Abstract read
In one paragraph

Article in Discover oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Shaobo Zhou *Department of Clinical Laboratory, China Medical University People's Hospital, The People's Hospital of Liaoning Province, Shenyang, China.
Na Li *Department of Clinical Laboratory, China Medical University People's Hospital, The People's Hospital of Liaoning Province, Shenyang, China.
Dina HaishaerDepartment of Clinical Laboratory, The First Affiliated Hospital of Fujian Medical University, Fuzhou, China.
Hongmei ZhaoHospital-Acquired Infection Control Department, China Medical University People's Hospital, The People's Hospital of Liaoning Province, Shenyang, China. 13889299493@126.com.

Funding

Wu Jieping Medical Foundation Special Fund for Clinical Research 320.6750.2021-06-5
6 · The paper itself

Abstract

backgroundLung cancer remains a leading global cause of mortality, with lung adenocarcinoma (LUAD) as the predominant histological subtype. Current serum biomarkers like carcinoembryonic antigen (CEA) lack specificity, necessitating novel diagnostic targets. Pentraxin 3 (PTX3), a homo-multimeric protein downregulated in malignancies, was evaluated for its diagnostic and prognostic roles in LUAD.

methodsPTX3 expression was analyzed using TCGA/GEO datasets and clinical serum samples (97 LUAD vs. 40 controls). Diagnostic utility was assessed via ROC curves for PTX3, CEACAM5, and their combination. Prognostic value was determined by Kaplan-Meier and Cox regression. PTX3-associated differentially expressed genes (DEGs) were explored through functional enrichment, tumor microenvironment (TME) analysis, and drug sensitivity profiling.

resultThe TCGA and GEO datasets revealed that PTX3 mRNA expression was significantly downregulated in LUAD, and the AUC values with PTX3 were > 0.7. Detection of CEACAM5 and PTX3 combined can improve diagnostic accuracy, and patients with high PTX3 level have shorter overall survival. Multivariate Cox analysis revealed that PTX3 is an independent predictor of overall survival. The result of ELISA further confirmed the low level of PTX3 protein. PTX3 is important in the functional analysis and TME of lung adenocarcinoma. In addition, the sensitivity of tumor cells to anti-cancer drugs is significantly correlated with the expression of PTX3.

conclusionPTX3 emerges as a dual biomarker for LUAD diagnosis and prognosis, with mechanistic ties to TME remodeling and therapeutic resistance, highlighting its potential for clinical translation.

Indexed as

DiagnosisImmuneLung adenocarcinomaPTX3

Identifiers

PMID40537732
PMCPMC12179049

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