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pmid:36187916

Recognition of immune-related tumor antigens and immune subtypes for mRNA vaccine development in lung adenocarcinoma.

Deze Zhao · Xianyu Liu · Yunhan Shan · JiaJia Li · Weifang Cui · Jun Wang · Junjie Jiang · Qun Xie · Chunfang Zhang · Chaojun Duan

Computational and structural biotechnology journal · 2022 doi:10.1016/j.csbj.2022.08.066

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Experiment

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Data

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Analysis

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title
Recognition of immune-related tumor antigens and immune subtypes for mRNA vaccine development in lung adenocarcinoma.
doi
10.1016/j.csbj.2022.08.066
pmid
36187916
authors array · 10 items
[0]
Deze Zhao
[1]
Xianyu Liu
[2]
Yunhan Shan
[3]
JiaJia Li
[4]
Weifang Cui
[5]
Jun Wang
[6]
Junjie Jiang
[7]
Qun Xie
[8]
Chunfang Zhang
[9]
Chaojun Duan
journal
Computational and structural biotechnology journal
year
2022
abstract
Background: There are currently no treatments targeting the immune microenvironment (TME) as an extension of immunotherapy. Our research aims to provide guidance for the development of immune-related mRNA vaccines and the identification of immune subtypes for vaccine treatment in lung adenocarcinoma (LUAD). Methods: HTRNA-Seq and single cell RNA-seq data were obtained from The Cancer Genome Atlas (TCGA) and Gene-Expression Omnibus (GEO, GSE87340, GSE140343, GSE148071) databases. Immune checkpoints (ICP) were used as criteria to differentiate immune subtypes and immune resistance score (IRS) system is constructed by ssGSEA to judge the immune microenvironment status of patients. Results: Two overexpressed tumor-specific antigens, including ZC3H12D and TXNDC5, were found to be associated with both disease-free survival (DFS) and overall survival (OS). In addition, the expression of two genes correlated with antigen-presenting cell (APC) infiltration and tumor purity. Subsequently, the immune subtype of the patient was defined by constructing an IRS scoring system. The lower the IRS, the stronger the immune response in the TME. This result was verified in external datasets and at the single-cell level. Conclusions: ZC3H12D and TXNDC5 are potential tumor-specific antigens for developing mRNA vaccines in LUAD. Importantly, patients with low IRS are more suitable for the use of immunotherapy and vaccines. Our research enhances understanding of TME features and guides more effective immunotherapy strategies.
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Univariate Cox regression was performed based on OS to find prognosis related ICGs. Then, enrichment score (ES) of risk ICGs (HR > 1) and protect ICGs (HR < 1) was calculated using single sample gene set enrichment analysis (ssGSEA) in the R package ‘GSVA’.
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sections[6] "Identification of immune subtypes" paragraph 2
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Univariate Cox regression was performed based on OS to find prognosis related ICGs. Then, enrichment score (ES) of risk ICGs (HR > 1) and protect ICGs (HR < 1) was calculated using single sample gene set enrichment analysis (ssGSEA) in the R package ‘GSVA’.
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The HTRNA-Seq, simple nucleotide variation, copy number variation data and related clinical information and single cell RNA sequencing data were described in method section “Data Extraction and Pre-processing”. All analyses were performed in R software. Specific content is explained in each section of Methods.
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ZC3H12D and TXNDC5 are potential tumor-specific antigens for developing mRNA vaccines in LUAD, and patients with low IRS are more suitable for immunotherapy and vaccines.
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ZC3H12D and TXNDC5 are potential tumor-specific antigens for developing mRNA vaccines in LUAD. Importantly, patients with low IRS are more suitable for the use of immunotherapy and vaccines. Our research enhances understanding of TME features and guides more effective immunotherapy strategies.
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ZC3H12D and TXNDC5 are potential tumor-specific antigens for developing mRNA vaccines in LUAD, and patients with low IRS are more suitable for immunotherapy and vaccines.
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sha256:1158afb53e0ca0219d21ca8b422fdc91db57e256a50dbe67e4d5d000e8a70684
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gaps array · 10 items
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asset:data:geo:GSE140343 licence not read
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asset:data:geo:GSE140343 not downloaded
[2]
asset:data:geo:GSE148071 licence not read
[3]
asset:data:geo:GSE148071 not downloaded
[4]
asset:data:geo:GSE87340 licence not read
[5]
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review.human_critique
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review.machine_critique
assays array · 2 items
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required_operations array · 0 items
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source_hashes object · 1 field
assay_lexicon
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confidence
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evidence array · 1 item
[0]
a (LUAD). Methods: HTRNA-Seq and single cell RNA-seq data were obtained from The Cancer Genome At
order_basis
paper_text_order:417
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assay:1
[1] object · 11 fields
role
analysis
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source_hashes object · 1 field
dsl_catalogue
f2132e96ae6c7a4e
evidence array · 1 item
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Univariate Cox regression was performed based on OS to find prognosis related ICGs. Then, enrichment score (ES) of risk ICGs (HR > 1) and protect ICGs (HR < 1) was calculated using single sample gene set enrichment analysis (ssGSEA) in the R package ‘GSVA’.
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Complete file
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Our research aims to provide guidance for the development of immune-related mRNA vaccines and the identification of immune subtypes for vaccine treatment in lung adenocarcinoma (LUAD).\nMethods: HTRNA-Seq and single cell RNA-seq data were obtained from The Cancer Genome Atlas (TCGA) and Gene-Expression Omnibus (GEO, GSE87340, GSE140343, GSE148071) databases. Immune checkpoints (ICP) were used as criteria to differentiate immune subtypes and immune resistance score (IRS) system is constructed by ssGSEA to judge the immune microenvironment status of patients.\nResults: Two overexpressed tumor-specific antigens, including ZC3H12D and TXNDC5, were found to be associated with both disease-free survival (DFS) and overall survival (OS). In addition, the expression of two genes correlated with antigen-presenting cell (APC) infiltration and tumor purity. Subsequently, the immune subtype of the patient was defined by constructing an IRS scoring system. The lower the IRS, the stronger the immune response in the TME. This result was verified in external datasets and at the single-cell level.\nConclusions: ZC3H12D and TXNDC5 are potential tumor-specific antigens for developing mRNA vaccines in LUAD. Importantly, patients with low IRS are more suitable for the use of immunotherapy and vaccines. Our research enhances understanding of TME features and guides more effective immunotherapy strategies.", "claims": [{"id": "claim-method", "statement": "Univariate Cox regression was performed based on OS to find prognosis related ICGs. 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Our research enhances understanding of TME features and guides more effective immunotherapy strategies."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": "ZC3H12D and TXNDC5 are potential tumor-specific antigens for developing mRNA vaccines in LUAD, and patients with low IRS are more suitable for immunotherapy and vaccines.", "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:36187916"], "outputs": ["the published estimate and its evidence"], "instruments": [], "reagents": []}, {"id": "obtain_source_data", "order": 2, "name": "Obtain the source data from the named repository", "kind": "data-preparation", "state": "complete", "blocked_on": null, "description": "The GEO series accession resolves and its sample accessions are listed. 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