Evidence map›Paper›PMID 42758874›Full record

ArticleFuture science OA2026

A two-gene prognostic model for lung adenocarcinoma using summary-data-based Mendelian randomization analysis and Cox proportional hazards regression.

Jing Xu, Xinyu Liu, Zhouxiao Lu, XiaoYu Wu, Xuzhou Yu, Sheng Wang

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Article in Future science OA, 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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5 · Who and what money

Authors and funding

6 authors.

Jing XuPharmacy Department, Jinhua People's Hospital, Jinhua, Zhejiang, 310053, China.
Xinyu LiuEndocrinology Department, Jinhua People's Hospital, Jinhua, Zhejiang, 310053, China.
Zhouxiao LuRespiratory Department, Zhejiang Jinhua Guangfu Cancer Hospital, Jinhua, Zhejiang, 310053, China.
XiaoYu WuRespiratory Department, Zhejiang Jinhua Guangfu Cancer Hospital, Jinhua, Zhejiang, 310053, China.
Xuzhou YuRespiratory Department, Zhejiang Jinhua Guangfu Cancer Hospital, Jinhua, Zhejiang, 310053, China.
Sheng WangRespiratory Department, Zhejiang Jinhua Guangfu Cancer Hospital, Jinhua, Zhejiang, 310053, China.ORCID 0000-0003-3300-2531

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsThis study aimed to develop accurate prognostic assessment tools for patients with lung adenocarcinoma (LUAD) using Summary-data-based Mendelian Randomization Analysis and statistical learning-based prognostic modeling methods.

methodsWe conducted SMR analysis to explore genetic associations between genes and LUAD, and analyzed differentially expressed genes (DEGs). The shared genes were subjected to the univariate Cox regression analysis and survival analysis to determine prognosis-related genes to construct a prognostic model with the multivariate Cox regression analysis. Individual gene contributions to the model were clarified through SHAP analysis, and predictive performance was assessed using the receiver operating characteristic curve, the C-index, and calibration plots.

results59 shared genes were identified between the SMR and DEGs analyses. The univariate Cox regression analysis and survival analysis identified two prognosis-related genes (PKP2 and SLC7A11), which were used to develop a prognostic model. The Kaplan-Meier plot and univariate and multivariate Cox regression models illustrated that patients in the high-risk group had a poorer clinical outcome. The low-risk group showed enrichment of several immune-related pathways and showed higher infiltration levels of 15 immune cell types.

conclusionA two-gene prognostic model was developed to predict outcomes in patients with LUAD, which was also highly associated with immune status.

Indexed as

PKP2prognostic modelshapley additive explanationsSLC7A11Summary-data-based mendelian randomization

Identifiers

PMID42758874
PMCPMC13596927

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