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pmid:38254708

Construction of a Novel Damage-Associated Molecular-Pattern-Related Signature to Assess Lung Adenocarcinoma's Prognosis and Immune Landscape.

Xinyue Liu · Shuxi Yao · Yanqi Feng · Piao Li · Yiming Li · Shu Xia

Biomolecules · 2024 doi:10.3390/biom14010108

Paper

complete

Experiment

complete

Data

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Analysis

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title
Construction of a Novel Damage-Associated Molecular-Pattern-Related Signature to Assess Lung Adenocarcinoma's Prognosis and Immune Landscape.
doi
10.3390/biom14010108
pmid
38254708
authors array · 6 items
[0]
Xinyue Liu
[1]
Shuxi Yao
[2]
Yanqi Feng
[3]
Piao Li
[4]
Yiming Li
[5]
Shu Xia
journal
Biomolecules
year
2024
abstract
Immunogenic death (ICD) stimulates adaptive immunity and affects immunotherapeutic efficacy, an important part of which is damage-associated molecular patterns (DAMPs). However, the function of these DAMPs for lung adenocarcinoma (LUAD) remains obscure. We initially found differentially expressed genes (DEGs) with prognostic significance related to DAMPs with the TCGA database and then used the least absolute shrinkage and selection operator (LASSO) regression to create a risk signature strongly correlated with overall survival (OS) with eight DEGs. Validation was performed externally using the external data set GSE68465. Lower-risk LUAD patients were found to be more chemotherapy-resistant and enriched for more immune-related pathways than those with higher risk scores, and patients with different risks showed different levels of immune cell infiltration. PANX1, a crucial gene closely associated with lung adenocarcinoma, was identified using the weighted correlation network analysis (WGCNA), and experiments revealed that PANX1 promotes the proliferation as well as invasion of LUAD cells. Furthermore, PANX1 was found to be positively correlated with CD274, CD276, and M2 macrophage markers. We developed and validated an entirely new gene signature related to DAMPs that may be useful for LUAD patient prognosis, immune microenvironment, and chemotherapeutic drug sensitivity prediction. The results may also guide clinical immunotherapy and chemotherapy approaches for LUAD patients.
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The least absolute shrinkage and selection operator (LASSO) Cox regression analysis was used to identify the genes and regression coefficients with the greatest predictive power after screening for prognostic DEGs with univariate Cox analysis and, finally, to build a risk signature on the most promising 8 genes.
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sections[5] "2.3. Assessment of a Risk Signature Based on DAMP-Associated Genes" paragraph 2
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The least absolute shrinkage and selection operator (LASSO) Cox regression analysis was used to identify the genes and regression coefficients with the greatest predictive power after screening for prognostic DEGs with univariate Cox analysis and, finally, to build a risk signature on the most promising 8 genes.
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The datasets used in this study can be found online as described above. The TCGA database is located at https://portal.gdc.cancer.gov, accessed on 3 December 2022, accession number: TCGA-LUAD; the GEO database is located at https://www.ncbi.nlm.nih.gov/gds, accessed on 3 December 2022, accession number: GSE68465.
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sections[39] "Data Availability Statement" paragraph 2
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The datasets used in this study can be found online as described above. The TCGA database is located at https://portal.gdc.cancer.gov, accessed on 3 December 2022, accession number: TCGA-LUAD; the GEO database is located at https://www.ncbi.nlm.nih.gov/gds, accessed on 3 December 2022, accession number: GSE68465.
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The study developed and validated an eight-gene DAMP-related risk signature for assessing prognosis, immune microenvironment, and chemotherapeutic drug sensitivity in lung adenocarcinoma patients.
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We developed and validated an entirely new gene signature related to DAMPs that may be useful for LUAD patient prognosis, immune microenvironment, and chemotherapeutic drug sensitivity prediction.
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The study developed and validated an eight-gene DAMP-related risk signature for assessing prognosis, immune microenvironment, and chemotherapeutic drug sensitivity in lung adenocarcinoma patients.
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The datasets used in this study can be found online as described above. The TCGA database is located at https://portal.gdc.cancer.gov, accessed on 3 December 2022, accession number: TCGA-LUAD; the GEO database is located at https://www.ncbi.nlm.nih.gov/gds, accessed on 3 December 2022, accession number: GSE68465.
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96
taxon
Homo sapiens
title
caArray_jacob-00182: Gene expression-based survival prediction in lung adenocarcinoma: a multi-site, blinded validation study
resolution_checked_at
2026-11-01T15:39:55Z
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The least absolute shrinkage and selection operator (LASSO) Cox regression analysis was used to identify the genes and regression coefficients with the greatest predictive power after screening for prognostic DEGs with univariate Cox analysis and, finally, to build a risk signature on the most promising 8 genes.
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basis
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 used in this study can be found online as described above. The TCGA database is located at https://portal.gdc.cancer.gov, accessed on 3 December 2022, accession number: TCGA-LUAD; the GEO database is located at https://www.ncbi.nlm.nih.gov/gds, accessed on 3 December 2022, accession number: GSE68465.
basis
The paper names GSE68465 in GEO database and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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er confirming the effectiveness of the PANX1 knockdown with PCR and Western blot assays (Figure 10B
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sfecting LUAD cell lines H1299 and H358 with siRNA-PANX1 to downregulate the expression of PANX
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tiveness of the PANX1 knockdown with PCR and Western blot assays (Figure 10B,C), we found the findings
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The least absolute shrinkage and selection operator (LASSO) Cox regression analysis was used to identify the genes and regression coefficients with the greatest predictive power after screening for prognostic DEGs with univariate Cox analysis and, finally, to build a risk signature on the most promising 8 genes.
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Complete file
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However, the function of these DAMPs for lung adenocarcinoma (LUAD) remains obscure. We initially found differentially expressed genes (DEGs) with prognostic significance related to DAMPs with the TCGA database and then used the least absolute shrinkage and selection operator (LASSO) regression to create a risk signature strongly correlated with overall survival (OS) with eight DEGs. Validation was performed externally using the external data set GSE68465. Lower-risk LUAD patients were found to be more chemotherapy-resistant and enriched for more immune-related pathways than those with higher risk scores, and patients with different risks showed different levels of immune cell infiltration. PANX1, a crucial gene closely associated with lung adenocarcinoma, was identified using the weighted correlation network analysis (WGCNA), and experiments revealed that PANX1 promotes the proliferation as well as invasion of LUAD cells. 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