Transcriptome characteristics of epithelial cells from advanced non‐small cell lung cancer were revealed by single‐cell RNA sequencing

Author:

Qiu Peng1ORCID,Chen Yutao2,Dong Cheng3,Xie Juanjuan4,Wang Junwu5

Affiliation:

1. Department of Rehabilitation First Affiliated Hospital of Wenzhou Medical University Wenzhou China

2. Department of Rehabilitation, The Second Affiliated Hospital and Yuying Children's Hospital Wenzhou Medical University Wenzhou China

3. Department of Rehabilitation Medicine, Ruijin Hospital Shanghai Jiao Tong University School of Medicine Shanghai China

4. Department of Cardiology First Affiliated Hospital of Wenzhou Medical University Wenzhou China

5. Department of Anesthesiology Second Affiliated Hospital of Zhejiang University School of Medicine Hangzhou China

Abstract

AbstractBackgroundLung adenocarcinoma (LUAD) is the prevalent malignancy worldwide. The aim is to explore differentially expressed genes (DEGs) associated with immune infiltration and survival time of LUAD patients, and predict transcriptional factors for shedding new light on molecular mechanisms and individual therapy of LUAD.MethodScRNA‐seq data of LUAD patients was downloaded from GSE148071 and analyzed by R packages. The clustering and protein–protein interaction network were constructed for screening DEGs. Gene Set Enrichment Analysis (GSEA) and GO enrichment analysis were performed in epithelial cell subgroups with high differentiation potential. Potential regulatory transcription factors were predicted.ResultsSixteen epithelial cell types were required and top 20 genes were identified on cell subgroup Epi4 with the highest differentiation potential associated with poor prognosis of LUAD in PPI network. GSEA and GO annotation results showed that cell subgroup Epi4 was enriched in the biological processes of cell proliferation and energy metabolism, and positively regulated the function of cell proliferation. TPI1 was significantly highly expressed in LUAD samples (p < .0001). TPI1 demonstrated a negative correlation with the infiltration levels of CD8+ T cells, CD4+ T cells, B cells, and activated mast cells, whilst manifesting a positive correlation with the infiltration levels of resident mast cells, Th2 cells, and MDSC. Epi4 was regulated by transcription factors MXD3 and GATA4.ConclusionOverexpression of TPI1 was identified as a novel biomarker for LUAD, and potential regulatory transcription factors MXD3 and GATA4 regulated the proliferation of LUAD with the poor prognosis, which may serve as potential targets to suppress the proliferation of LUAD.

Publisher

Wiley

Subject

Health, Toxicology and Mutagenesis,Management, Monitoring, Policy and Law,Toxicology,General Medicine

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