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Estimation of immune cell content in tumor using single-cell RNA-seq reference data.

AbstractBACKGROUND:
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.
AuthorsXiaoqing Yu, Y Ann Chen, Jose R Conejo-Garcia, Christine H Chung, Xuefeng Wang
JournalBMC cancer (BMC Cancer) Vol. 19 Issue 1 Pg. 715 (Jul 19 2019) ISSN: 1471-2407 [Electronic] England
PMID31324168 (Publication Type: Journal Article)
Chemical References
  • RNA, Small Cytoplasmic
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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