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pmid:35620271

Intercellular Communication-Related Molecular Subtypes and a Gene Signature Identified by the Single-Cell RNA Sequencing Combined with a Transcriptomic Analysis.

Pin Guan · Wentao Cai · Ke Wu · Fan Jiang · Jinchan Wu · Xin Zhai · Min Zeng

Disease markers · 2022 doi:10.1155/2022/6837849

Paper

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Experiment

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Data

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title
Intercellular Communication-Related Molecular Subtypes and a Gene Signature Identified by the Single-Cell RNA Sequencing Combined with a Transcriptomic Analysis.
doi
10.1155/2022/6837849
pmid
35620271
authors array · 7 items
[0]
Pin Guan
[1]
Wentao Cai
[2]
Ke Wu
[3]
Fan Jiang
[4]
Jinchan Wu
[5]
Xin Zhai
[6]
Min Zeng
journal
Disease markers
year
2022
abstract
Background: The tumor microenvironment (TME) of lung adenocarcinoma (LUAD) comprise various cell types that communicate with each other through ligand-receptor interactions. This study focused on the identification of cell types in LUAD by single-cell RNA sequencing (scRNA-seq) data and screening of intercellular communication-related genes. Methods: The Gene Expression Omnibus (GEO) database (https://www.ncbi.nlm.nih.gov/geo) provided the RNA-seq data of LUAD patients in the GSE149655, GSE31210, and GSE72094 datasets. Quality control of the scRNA-seq data in GSE149655 was performed by the Seurat package (http://seurat.r-forge.r-project.org) for identifying highly variable genes for principal component analysis (PCA) and cell clustering. The CellPhoneDB (http://www.cellphonedb.org) was used for filtering intercellular communication-related ligand-receptor pairs. According to ligand and receptor expressions, LUAD samples were clustered using ConsensusClusterPlus (https://www.bioconductor.org/packages/release/bioc/html/ConsensusClusterPlus). Additionally, the identification of prognosis-related ligand and receptor genes was conducted along with the development of a risk prediction model by the least absolute shrinkage and selection operator (LASSO) Cox regression analysis. Results: This study identified twelve cell types in 8170 cells of LUAD tissues along with 219 ligand and receptor genes. LUAD was classified into three different molecular subtypes, among which cluster 3 (C3) had the longest overall survival (OS) time and cluster (C1) had the shortest OS time. In comparison with the other two molecular subtypes, it was observed that C1 had a higher rate of somatic mutations and lower levels of infiltrating immune cells and immune scores. Ten genes were screened from the total ligand and receptor genes to construct a risk model, which showed a strong prediction power in the prognosis of patients with LUAD. Conclusion: The results of this study revealed cell types specific to LUAD, which were classified into different molecular subtypes according to intercellular communication-related genes. A novel prognostic risk model was developed in this study, providing new insights into prognostic assessment models for LUAD.
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Additionally, the identification of prognosis-related ligand and receptor genes was conducted along with the development of a risk prediction model by the least absolute shrinkage and selection operator (LASSO) Cox regression analysis.
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Additionally, the identification of prognosis-related ligand and receptor genes was conducted along with the development of a risk prediction model by the least absolute shrinkage and selection operator (LASSO) Cox regression analysis.
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A novel prognostic risk model was developed in this study, providing new insights into prognostic assessment models for LUAD.
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A novel prognostic risk model was developed in this study, providing new insights into prognostic assessment models for LUAD.
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A novel prognostic risk model was developed in this study, providing new insights into prognostic assessment models for LUAD.
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Single cell RNAseq of human early stage lung adenocarcinoma with activating somatic KRAS mutations and associated normal lung tissues reveals alterations of key gene expression in alveolar type II pneumocytes
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KRAS mutation-associated gene expression, p53 and STK11 mutations, proliferation and immune surveillance in lung adenocarcinoma
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Additionally, the identification of prognosis-related ligand and receptor genes was conducted along with the development of a risk prediction model by the least absolute shrinkage and selection operator (LASSO) Cox regression analysis.
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types and a Gene Signature Identified by the Single-Cell RNA Sequencing Combined with a Transcriptomic Analysis.
[1]
the identification of cell types in LUAD by single-cell RNA sequencing (scRNA-seq) data and screening of intercellu
[2]
types in LUAD by single-cell RNA sequencing (scRNA-seq) data and screening of intercellular communi
[3]
nd GSE72094 datasets. Quality control of the scRNA-seq data in GSE149655 was performed by the Seura
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Gene Signature Identified by the Single-Cell RNA Sequencing Combined with a Transcriptomic Analysis.
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e Single-Cell RNA Sequencing Combined with a Transcriptomic Analysis.
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tps://www.ncbi.nlm.nih.gov/geo) provided the RNA-seq data of LUAD patients in the GSE149655, GSE3
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ication of cell types in LUAD by single-cell RNA sequencing (scRNA-seq) data and screening of intercellu
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2M checkpoint. The inhibited P53 pathway and apoptosis were well recognized pathways (Figure 5(a)).
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Additionally, the identification of prognosis-related ligand and receptor genes was conducted along with the development of a risk prediction model by the least absolute shrinkage and selection operator (LASSO) Cox regression analysis.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:35620271", "kind": "science-record", "revision": 3, "content_hash": "sha256:cacd5cf12dbc49a9ab8bbbc8581ef1adf0d211ea9e4566274426efc83990f15c", "created_at": "2026-11-01T18:14:32Z", "updated_at": "2026-11-01T21:27:57Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Intercellular Communication-Related Molecular Subtypes and a Gene Signature Identified by the Single-Cell RNA Sequencing Combined with a Transcriptomic Analysis.", "doi": "10.1155/2022/6837849", "pmid": "35620271", "authors": ["Pin Guan", "Wentao Cai", "Ke Wu", "Fan Jiang", "Jinchan Wu", "Xin Zhai", "Min Zeng"], "journal": "Disease markers", "year": 2022, "abstract": "Background: The tumor microenvironment (TME) of lung adenocarcinoma (LUAD) comprise various cell types that communicate with each other through ligand-receptor interactions. This study focused on the identification of cell types in LUAD by single-cell RNA sequencing (scRNA-seq) data and screening of intercellular communication-related genes.\nMethods: The Gene Expression Omnibus (GEO) database (https://www.ncbi.nlm.nih.gov/geo) provided the RNA-seq data of LUAD patients in the GSE149655, GSE31210, and GSE72094 datasets. Quality control of the scRNA-seq data in GSE149655 was performed by the Seurat package (http://seurat.r-forge.r-project.org) for identifying highly variable genes for principal component analysis (PCA) and cell clustering. The CellPhoneDB (http://www.cellphonedb.org) was used for filtering intercellular communication-related ligand-receptor pairs. According to ligand and receptor expressions, LUAD samples were clustered using ConsensusClusterPlus (https://www.bioconductor.org/packages/release/bioc/html/ConsensusClusterPlus). Additionally, the identification of prognosis-related ligand and receptor genes was conducted along with the development of a risk prediction model by the least absolute shrinkage and selection operator (LASSO) Cox regression analysis.\nResults: This study identified twelve cell types in 8170 cells of LUAD tissues along with 219 ligand and receptor genes. LUAD was classified into three different molecular subtypes, among which cluster 3 (C3) had the longest overall survival (OS) time and cluster (C1) had the shortest OS time. In comparison with the other two molecular subtypes, it was observed that C1 had a higher rate of somatic mutations and lower levels of infiltrating immune cells and immune scores. Ten genes were screened from the total ligand and receptor genes to construct a risk model, which showed a strong prediction power in the prognosis of patients with LUAD.\nConclusion: The results of this study revealed cell types specific to LUAD, which were classified into different molecular subtypes according to intercellular communication-related genes. 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