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pmid:39465750

Prognostic value of a lactate metabolism gene signature in lung adenocarcinoma and its associations with immune checkpoint blockade therapy response.

Tengfei Huang · DuoHuang Lian · MengMeng Chen · YaMing Liu · MeiQing Zhang · DeHua Zeng · Shun-Kai Zhou · WenMin Ying

Medicine · 2024 doi:10.1097/MD.0000000000039371

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Experiment

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Data

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:39465750
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2026-11-01T20:29:43Z
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2026-11-01T21:34:14Z
generator object · 2 fields
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paper object · 10 fields
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complete
title
Prognostic value of a lactate metabolism gene signature in lung adenocarcinoma and its associations with immune checkpoint blockade therapy response.
doi
10.1097/MD.0000000000039371
pmid
39465750
authors array · 8 items
[0]
Tengfei Huang
[1]
DuoHuang Lian
[2]
MengMeng Chen
[3]
YaMing Liu
[4]
MeiQing Zhang
[5]
DeHua Zeng
[6]
Shun-Kai Zhou
[7]
WenMin Ying
journal
Medicine
year
2024
abstract
Lung adenocarcinoma (LUAD) is a study that examines the prognostic value of lactate metabolism genes in tumor cells, which are associated with clinical prognosis. We analyzed the expression and clinical data for LUAD from The Cancer Genome Atlas database, using the GSE68465 dataset from the Gene Expression Omnibus and the MSigDB database. LASSO Cox regression and stepwise Cox regression were used to identify the optimal lactate metabolism gene signature. Differences in immune infiltration, tumor mutation burden (TMB), and response to immune checkpoint blockade (ICB) therapy were evaluated between groups. LASSO and Cox regression analyses showed an eight-lactate metabolism gene signature for model construction in both TCGA cohort and GSE68465 data, with higher survival outcomes in high-risk groups. The lactate metabolism risk score had an independent prognostic value (hazard ratio: 2.279 [1.652-3.146], P < .001). Immune cell infiltration differed between the risk groups, such as CD8+ T cells, macrophages, dendritic cells, mast cells, and neutrophils. The high-risk group had higher tumor purity, lower immune and stromal scores, and higher TMB. High-risk samples had high tumor immune dysfunction and exclusion (TIDE) scores and low cytolytic activity (CYT) scores, indicating a poor response to ICB therapy. Similarly, most immune checkpoint molecules, immune inhibitors/stimulators, and major histocompatibility complex (MHC) molecules were highly expressed in the high-risk group. The 8-lactate metabolism gene-based prognostic model predicts patient survival, immune infiltration, and ICB response in patients with LUAD, driving the development of therapeutic strategies to target lactate metabolism.
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Univariate Cox regression analysis provided in the Survival package (version 2.41-1) was applied to screen prognosis-associated lactate metabolism genes and genes with P < .05. The LASSO Cox regression analysis provided in the lars package (version 1.2) determined the best weighting coefficient for prognosis-associated lactate metabolism genes.
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methodological
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sections[6] "2.3. Establishment and validation of lactate metabolism-related risk score model" paragraph 2
quote
Univariate Cox regression analysis provided in the Survival package (version 2.41-1) was applied to screen prognosis-associated lactate metabolism genes and genes with P < .05. The LASSO Cox regression analysis provided in the lars package (version 1.2) determined the best weighting coefficient for prognosis-associated lactate metabolism genes.
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The datasets generated during and/or analyzed during the current study are publicly available.
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sections[23] "(untitled)" paragraph 1
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The datasets generated during and/or analyzed during the current study are publicly available.
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LASSO and Cox regression analyses showed an eight-lactate metabolism gene signature for model construction in both TCGA cohort and GSE68465 data, with higher survival outcomes in high-risk groups.
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qualitative
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null
evidence array · 1 item
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sections[0] "Abstract" paragraph 1
quote
LASSO and Cox regression analyses showed an eight-lactate metabolism gene signature for model construction in both TCGA cohort and GSE68465 data, with higher survival outcomes in high-risk groups.
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complete
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experiment object · 8 fields
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LASSO and Cox regression analyses showed an eight-lactate metabolism gene signature for model construction in both TCGA cohort and GSE68465 data, with higher survival outcomes in high-risk groups.
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title
caArray_jacob-00182: Gene expression-based survival prediction in lung adenocarcinoma: a multi-site, blinded validation study
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2026-11-01T15:39:55Z
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Univariate Cox regression analysis provided in the Survival package (version 2.41-1) was applied to screen prognosis-associated lactate metabolism genes and genes with P < .05. The LASSO Cox regression analysis provided in the lars package (version 1.2) determined the best weighting coefficient for prognosis-associated lactate metabolism genes.
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Automated Assays Laravel application and simulated adapters
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The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: cox_proportional_hazards.
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The datasets generated during and/or analyzed during the current study are publicly available.
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Univariate Cox regression analysis provided in the Survival package (version 2.41-1) was applied to screen prognosis-associated lactate metabolism genes and genes with P < .05. The LASSO Cox regression analysis provided in the lars package (version 1.2) determined the best weighting coefficient for prognosis-associated lactate metabolism genes.
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We analyzed the expression and clinical data for LUAD from The Cancer Genome Atlas database, using the GSE68465 dataset from the Gene Expression Omnibus and the MSigDB database. LASSO Cox regression and stepwise Cox regression were used to identify the optimal lactate metabolism gene signature. Differences in immune infiltration, tumor mutation burden (TMB), and response to immune checkpoint blockade (ICB) therapy were evaluated between groups. LASSO and Cox regression analyses showed an eight-lactate metabolism gene signature for model construction in both TCGA cohort and GSE68465 data, with higher survival outcomes in high-risk groups. The lactate metabolism risk score had an independent prognostic value (hazard ratio: 2.279 [1.652-3.146], P < .001). Immune cell infiltration differed between the risk groups, such as CD8+ T cells, macrophages, dendritic cells, mast cells, and neutrophils. The high-risk group had higher tumor purity, lower immune and stromal scores, and higher TMB. High-risk samples had high tumor immune dysfunction and exclusion (TIDE) scores and low cytolytic activity (CYT) scores, indicating a poor response to ICB therapy. Similarly, most immune checkpoint molecules, immune inhibitors/stimulators, and major histocompatibility complex (MHC) molecules were highly expressed in the high-risk group. The 8-lactate metabolism gene-based prognostic model predicts patient survival, immune infiltration, and ICB response in patients with LUAD, driving the development of therapeutic strategies to target lactate metabolism.", "claims": [{"id": "claim-method", "statement": "Univariate Cox regression analysis provided in the Survival package (version 2.41-1) was applied to screen prognosis-associated lactate metabolism genes and genes with P < .05. 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