Identifying ADME-related gene signature for immune landscape and prognosis in KIRC by single-cell and spatial transcriptome analysis

Abstract Kidney renal clear cell carcinoma (KIRC) is the most prevalent subtype of kidney cancer. Although multiple therapeutic agents have been proven effective in KIRC, their clinical application has been hindered by a lack of reliable biomarkers. This study focused on the prognostic value and fun...

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Main Authors: Hongyun Wang, Feizhou Li, Qiong Wang, Xinyuan Guo, Xinbing Chen, Xinrong Zou, Jun Yuan
Format: Article
Language:English
Published: Nature Portfolio 2025-01-01
Series:Scientific Reports
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Online Access:https://doi.org/10.1038/s41598-024-84018-7
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author Hongyun Wang
Feizhou Li
Qiong Wang
Xinyuan Guo
Xinbing Chen
Xinrong Zou
Jun Yuan
author_facet Hongyun Wang
Feizhou Li
Qiong Wang
Xinyuan Guo
Xinbing Chen
Xinrong Zou
Jun Yuan
author_sort Hongyun Wang
collection DOAJ
description Abstract Kidney renal clear cell carcinoma (KIRC) is the most prevalent subtype of kidney cancer. Although multiple therapeutic agents have been proven effective in KIRC, their clinical application has been hindered by a lack of reliable biomarkers. This study focused on the prognostic value and function of drug absorption, distribution, metabolism, and excretion- (ADME-) related genes (ARGs) in KIRC to enhance personalized therapy. The critical role of ARGs in KIRC microenvironment was confirmed by single cell RNA-seq analysis and spatial transcriptome sequencing analysis for the first time. Then, an ADME-related prognostic signature (ARPS) was developed by the bulk RNA-seq analysis. The ARPS, created through Cox regression, LASSO, and stepAIC analyses, identified eight ARGs that stratified patients into high-risk and low-risk groups. High-risk patients had significantly poorer overall survival. Multivariate analysis confirmed the independent predictive ability of ARPS, and an ARPS-based nomogram was constructed for clinical application. Gene ontology and KEGG pathway analyses revealed immune-related functions and pathways enriched in these groups, with low-risk patients showing better responses to immunotherapy. Finally, the expression of ARGs was validated by qRT-PCR and Western blotting experiments. These findings underscore the prognostic significance of ARPS in KIRC and its potential application in guiding personalized treatment strategies.
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spelling doaj-art-72887eb54c3a40f2920473b6c41bfd252025-01-12T12:22:58ZengNature PortfolioScientific Reports2045-23222025-01-0115112210.1038/s41598-024-84018-7Identifying ADME-related gene signature for immune landscape and prognosis in KIRC by single-cell and spatial transcriptome analysisHongyun Wang0Feizhou Li1Qiong Wang2Xinyuan Guo3Xinbing Chen4Xinrong Zou5Jun Yuan6Hubei Provincial Hospital of Traditional Chinese Medicine, Affiliated Hospital of Hubei University of Chinese MedicineHubei Provincial Hospital of Traditional Chinese Medicine, Affiliated Hospital of Hubei University of Chinese MedicineHubei University of Chinese MedicineHubei University of Chinese MedicineHubei University of Chinese MedicineHubei Provincial Hospital of Traditional Chinese Medicine, Affiliated Hospital of Hubei University of Chinese MedicineDepartment of Nephrology, Renmin Hospital of Wuhan UniversityAbstract Kidney renal clear cell carcinoma (KIRC) is the most prevalent subtype of kidney cancer. Although multiple therapeutic agents have been proven effective in KIRC, their clinical application has been hindered by a lack of reliable biomarkers. This study focused on the prognostic value and function of drug absorption, distribution, metabolism, and excretion- (ADME-) related genes (ARGs) in KIRC to enhance personalized therapy. The critical role of ARGs in KIRC microenvironment was confirmed by single cell RNA-seq analysis and spatial transcriptome sequencing analysis for the first time. Then, an ADME-related prognostic signature (ARPS) was developed by the bulk RNA-seq analysis. The ARPS, created through Cox regression, LASSO, and stepAIC analyses, identified eight ARGs that stratified patients into high-risk and low-risk groups. High-risk patients had significantly poorer overall survival. Multivariate analysis confirmed the independent predictive ability of ARPS, and an ARPS-based nomogram was constructed for clinical application. Gene ontology and KEGG pathway analyses revealed immune-related functions and pathways enriched in these groups, with low-risk patients showing better responses to immunotherapy. Finally, the expression of ARGs was validated by qRT-PCR and Western blotting experiments. These findings underscore the prognostic significance of ARPS in KIRC and its potential application in guiding personalized treatment strategies.https://doi.org/10.1038/s41598-024-84018-7Kidney renal clear cell carcinomaADME genesGene signatureSurvivalImmune cell infiltration
spellingShingle Hongyun Wang
Feizhou Li
Qiong Wang
Xinyuan Guo
Xinbing Chen
Xinrong Zou
Jun Yuan
Identifying ADME-related gene signature for immune landscape and prognosis in KIRC by single-cell and spatial transcriptome analysis
Scientific Reports
Kidney renal clear cell carcinoma
ADME genes
Gene signature
Survival
Immune cell infiltration
title Identifying ADME-related gene signature for immune landscape and prognosis in KIRC by single-cell and spatial transcriptome analysis
title_full Identifying ADME-related gene signature for immune landscape and prognosis in KIRC by single-cell and spatial transcriptome analysis
title_fullStr Identifying ADME-related gene signature for immune landscape and prognosis in KIRC by single-cell and spatial transcriptome analysis
title_full_unstemmed Identifying ADME-related gene signature for immune landscape and prognosis in KIRC by single-cell and spatial transcriptome analysis
title_short Identifying ADME-related gene signature for immune landscape and prognosis in KIRC by single-cell and spatial transcriptome analysis
title_sort identifying adme related gene signature for immune landscape and prognosis in kirc by single cell and spatial transcriptome analysis
topic Kidney renal clear cell carcinoma
ADME genes
Gene signature
Survival
Immune cell infiltration
url https://doi.org/10.1038/s41598-024-84018-7
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