Abstract | BACKGROUND: The rapid development of single-cell RNA sequencing ( scRNA-seq) provides unprecedented opportunities to study the tumor ecosystem that involves a heterogeneous mixture of cell types. However, the majority of previous and current studies related to translational and molecular oncology have only focused on the bulk tumor and there is a wealth of gene expression data accumulated with matched clinical outcomes. RESULTS: In this paper, we introduce a scheme for characterizing cell compositions from bulk tumor gene expression by integrating signatures learned from scRNA-seq data. We derived the reference expression matrix to each cell type based on cell subpopulations identified in head and neck cancer dataset. Our results suggest that scRNA-Seq-derived reference matrix outperforms the existing gene panel and reference matrix with respect to distinguishing immune cell subtypes. CONCLUSIONS: Findings and resources created from this study enable future and secondary analysis of tumor RNA mixtures in head and neck cancer for a more accurate cellular deconvolution, and can facilitate the profiling of the immune infiltration in other solid tumors due to the expression homogeneity observed in immune cells.
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Authors | Xiaoqing Yu, Y Ann Chen, Jose R Conejo-Garcia, Christine H Chung, Xuefeng Wang |
Journal | BMC cancer
(BMC Cancer)
Vol. 19
Issue 1
Pg. 715
(Jul 19 2019)
ISSN: 1471-2407 [Electronic] England |
PMID | 31324168
(Publication Type: Journal Article)
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Chemical References |
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Topics |
- CD8-Positive T-Lymphocytes
(immunology)
- Databases, Genetic
- Datasets as Topic
- Ecosystem
- Genes, Neoplasm
- Genetic Heterogeneity
- Head and Neck Neoplasms
(genetics, immunology, pathology)
- Humans
- RNA, Small Cytoplasmic
(genetics)
- RNA-Seq
(methods)
- Single-Cell Analysis
(methods)
- Software
- Squamous Cell Carcinoma of Head and Neck
(genetics, immunology, pathology)
- T-Lymphocytes, Regulatory
(immunology)
- Transcriptome
- Tumor Microenvironment
(genetics, immunology)
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