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pmid:36157879
Single-Cell Transcriptome Analysis Reveals Different Immune Signatures in HPV- and HPV + Driven Human Head and Neck Squamous Cell Carcinoma.
Simin Li · Yang Wang · Rui Sun · Debora Franceschi · Hongying Pan · Chenxuan Wei · Anthony Chukwunonso Ogbuehi · Bernd Lethaus · Vuk Savkovic · Sebastian Gaus · Rüdiger Zimmerer · Dirk Ziebolz · Gerhard Schmalz · Xiao Jiang
Journal of immunology research · 2022 doi:10.1155/2022/2079389
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Experiment
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Data
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Analysis
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Execution
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Complete file
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Following data normalization, all highly variable genes in single cells were identified, and batch correction was applied. Differentially expressed genes were identified using Wilcoxon rank sum test. A gene enrichment analysis was performed in each cell cluster using KEGG analysis. Single-cell pseudotime trajectories were constructed with MONOCLE (version 2.6.4). Cell-cell interactions were analyzed with CellChat R package. Additionally, cell-cell communication patterns in key signal pathways were compared in different tissue groups. A hidden Markov model (HMM) was used to predict gene expression states (on or off) throughout pseudotime. Five-year overall survival outcomes were compared in both HPV+ and HPV- subsets.\nResults: 20,978 high-quality individual cells passed quality control. RNA-seq data were used from 522 HNSCC primary tumor samples. 1,137 differentially expressed genes between HPV+ and HPV- HNSCC patients were investigated. 96 differentially expressed genes were associated with overall survival and highly enriched in B cell associated biological process. Cell composition differed between types of samples. MHC-I, MHC-II, and MIF signaling pathways were found to be most relevant. Within these pathways, some cells were either signal receiver or signal sender, depending on sample type, respectively. Six genes were obtained, AREG and TGFBI (upregulation), CD27, CXCR3, MS4A1, and CD19 (downregulation), whose expression and HPV types were highly associated with worse overall survival. AREG and TGFBI were pDC marker genes, CXCR3 and CD27 were significantly expressed in T cell-related cells, while MS4A1 and CD19 were mainly expressed in B naïve cells.\nConclusions: This study revealed dynamic changes in cell percentage and heterogeneity of cell subtypes of HNSCC. AREG, TGFBI, CD27, CXCR3, MS4A1, and CD19 were associated with worse overall survival in HPV-related HNSCC. Especially B-cell related pathways were revealed as particularly relevant in HPV-related HNSCC. 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RNA-seq data were used from 522 HNSCC primary tumor", "l Survival Compared with HPV- HNSCC Patients RNA-seq data were used from 522 HNSCC primary tumor", "mmune microenvironment of HNSCC, single-cell RNA sequencing analysis was performed on the samples from d"], "order_basis": "paper_text_order:0", "id": "assay:1"}, {"role": "data_generation", "definition_id": "scrna_seq", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "unsupported", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.99, "evidence": ["define the immune microenvironment of HNSCC, single-cell RNA sequencing analysis was performed on the samples from d", "immune cells were identified (Figure 1(a)). Single-cell RNA sequencing results from immune cells in HNSCC. 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