Evidence map›Paper›PMID 41029063›Full record

ArticleMedicine2025

Comprehensive investigation of a new signature integrating lipid metabolism and immune-related genes for clear cell renal cell carcinoma prognosis and immunometabolism landscapes.

Zhenyu Mu, Haizhu Fu, Shanchun Guo, Zhaoming Zhang, Zhiqiang Wang, Haixia Wang, Jiangxia Yin

Abstract read
In one paragraph

Article in Medicine, 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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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

7 authors.

Zhenyu MuDepartment of Traditional Chinese Medicine, Affiliated Hospital of Shandong Second Medical University, School of Clinical Medicine, Shandong Second Medical University, Weifang, China.
Haizhu FuDepartment of Urology, Shouguang Hospital of Traditional Chinese Medicine, Shouguang, China.
Shanchun GuoRCMI Cancer Research Center, Xavier University of Louisiana, New Orleans, LA.ORCID 0000-0002-3593-3738
Zhaoming ZhangDepartment of Basic Medicine, Xinjiang Second Medical College, Kelamayi, Xinjiang, China.
Zhiqiang WangDepartment of Urology, Shouguang Hospital of Traditional Chinese Medicine, Shouguang, China.
Haixia WangDepartment of Traditional Chinese Medicine, Affiliated Hospital of Shandong Second Medical University, School of Clinical Medicine, Shandong Second Medical University, Weifang, China.
Jiangxia YinDepartment of Medical Oncology, Shouguang Hospital of Traditional Chinese Medicine, Shouguang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multi-omics studies have significantly advanced our understanding of ccRCC. These studies have revealed that aggressive ccRCC is closely associated with metabolic reprogramming, particularly involving lipid metabolism. Recent studies have highlighted the crosstalk between lipid metabolism and immune function in the tumor microenvironment (TME) of ccRCC. However, prognostic models integrating both pathways remain underdeveloped. A detailed analysis was conducted on the varied lipid metabolism subtypes utilizing 638 records of clear cell renal cell carcinoma from the Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) databases, focusing on lipid metabolism genes and immune-related genes (LRGs). The clinical importance, functional status, TME interaction, and genetic alterations of various subtypes were further investigated. A novel grading system, the lipid-immune score (LIS), was created and validated. Two distinct subgroups, characterized by elevated expression of lipid metabolism genes and exhibiting traits of tumor metabolism and proliferation, are classified as lipid metabolism phenotypes. The lipid metabolism phenotype exhibits a more favorable prognosis, enhanced anti-tumor immunity, and increased sensitivity to immunotherapy. The expression of more LRGs, the enrichment of immunoreactive pathways, and the infiltration of effector immune cells are characterized as immunoreactive phenotypes. The prognosis for the immunoactive phenotype is unfavorable and is more prevalent in patients experiencing tumor progression. Furthermore, BAP1 is a pivotal mutant gene in the immunoactive subtype. LIS was ultimately shown as a reliable predictor of overall survival (OS) and immunotherapy outcomes in patients with clear cell renal cell carcinoma. We systematically analyzed immune- and lipid metabolism-related genes, identifying 2 distinct molecular subtypes with differing biological functions, immune profiles, and clinical outcomes. We also developed a LIS that effectively predicts patient prognosis and immunotherapy response, offering a new strategy for precision medicine in ccRCC. Our research elucidates the relationship between lipid metabolism and immune response, offering a distinctive strategy for therapeutic management and precision medicine in patients with clear cell renal cell carcinoma.

Indexed as

Carcinoma, Renal CellKidney NeoplasmsLipid MetabolismBiomarkers, TumorFemaleGene Expression Regulation, NeoplasticHumansMalePrognosisTumor MicroenvironmentTumor Suppressor ProteinsUbiquitin ThiolesteraseBAP1 protein, humanBiomarkers, TumorTumor Suppressor ProteinsUbiquitin Thiolesterasebioinformaticsclear cell renal cell carcinomaGEO databaseimmunelipid metabolismTCGA database

Identifiers

PMID41029063
PMCPMC13593055

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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.