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pmid:36728032

Development and validation of an immune-related gene signature for prognosis in Lung adenocarcinoma.

Zehuai Guo · Xiangjun Qi · Zeyun Li · Jianying Yang · Zhe Sun · Peiqin Li · Ming Chen · Yang Cao

IET systems biology · 2023 doi:10.1049/syb2.12057

Paper

complete

Experiment

complete

Data

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Analysis

complete

Execution

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title
Development and validation of an immune-related gene signature for prognosis in Lung adenocarcinoma.
doi
10.1049/syb2.12057
pmid
36728032
authors array · 8 items
[0]
Zehuai Guo
[1]
Xiangjun Qi
[2]
Zeyun Li
[3]
Jianying Yang
[4]
Zhe Sun
[5]
Peiqin Li
[6]
Ming Chen
[7]
Yang Cao
journal
IET systems biology
year
2023
abstract
The most common type of lung cancer tissue is lung adenocarcinoma. The TCGA-LUAD cohort retrieved from the TCGA dataset was considered the internal training cohort, while GSE68465 and GSE13213 datasets from the GEO database were used as the external test cohort. The TCGA-LUAD cohort was classified into two immune subtypes using single-sample gene set enrichment analysis of the immune gene set and unsupervised clustering analysis. The ESTIMATE algorithm, the CIBERSORT algorithm, and HLA family expression levels again validated the reliability of this typing. We performed Venn analysis using immune-related genes from the immport dataset and differentially expressed genes from the subtypes to retrieve differentially expressed immune genes (DEIGs). In addition, DEIGs were used to construct a prognostic model with the least absolute shrinkage and selection operator regression analysis. A reliable risk model consisting of 11 DEIGs, including S100P, INHA, SEMA7A, INSL4, CD40LG, AGER, SERPIND1, CD1D, CX3CR1, SFTPD, and CD79A, was then built, and its reliability was further confirmed by ROC curve and calibration plot analysis. The high-risk score subgroup had a poor prognosis and a lower tumour immune dysfunction and exclusion score, indicating a greater likelihood of anti-PD-1/cytotoxic T lymphocyte antigen 4 benefit.
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Premised on p < 0.01, univariate Cox regression analysis revealed 37 genes in the training cohort (Figure 4c). Following that, the LASSO Cox regression method was executed (Figure 4d,e).
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sections[14] "Prognosis models of DEIGs" paragraph 2
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Premised on p < 0.01, univariate Cox regression analysis revealed 37 genes in the training cohort (Figure 4c). Following that, the LASSO Cox regression method was executed (Figure 4d,e).
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The data that support the findings of this study are openly available in NCBI Gene Expression Omnibus at https://www.ncbi.nlm.nih.gov/geo/, The Cancer Genome Atlas Program at https://portal.gdc.cancer.gov/repository, and ImmPort Portal database at https://www.immport.org/.
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sections[26] "DATA AVAILABILITY STATEMENT" paragraph 2
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The data that support the findings of this study are openly available in NCBI Gene Expression Omnibus at https://www.ncbi.nlm.nih.gov/geo/, The Cancer Genome Atlas Program at https://portal.gdc.cancer.gov/repository, and ImmPort Portal database at https://www.immport.org/.
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A reliable risk model consisting of 11 DEIGs, including S100P, INHA, SEMA7A, INSL4, CD40LG, AGER, SERPIND1, CD1D, CX3CR1, SFTPD, and CD79A, was then built, and its reliability was further confirmed by ROC curve and calibration plot analysis.
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A reliable risk model consisting of 11 DEIGs, including S100P, INHA, SEMA7A, INSL4, CD40LG, AGER, SERPIND1, CD1D, CX3CR1, SFTPD, and CD79A, was then built, and its reliability was further confirmed by ROC curve and calibration plot analysis.
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A reliable risk model consisting of 11 DEIGs, including S100P, INHA, SEMA7A, INSL4, CD40LG, AGER, SERPIND1, CD1D, CX3CR1, SFTPD, and CD79A, was then built, and its reliability was further confirmed by ROC curve and calibration plot analysis.
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Relapse-related molecular signature in lung adenocarcinomas identifies patients with dismal prognosis
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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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Premised on p < 0.01, univariate Cox regression analysis revealed 37 genes in the training cohort (Figure 4c). Following that, the LASSO Cox regression method was executed (Figure 4d,e).
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The data that support the findings of this study are openly available in NCBI Gene Expression Omnibus at https://www.ncbi.nlm.nih.gov/geo/, The Cancer Genome Atlas Program at https://portal.gdc.cancer.gov/repository, and ImmPort Portal database at https://www.immport.org/.
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Premised on p < 0.01, univariate Cox regression analysis revealed 37 genes in the training cohort (Figure 4c). Following that, the LASSO Cox regression method was executed (Figure 4d,e).
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