Dissecting the Single-Cell Transcriptome Network Underlying Gastric Premalignant Lesions and Early Gastric Cancer

Cell Rep. 2019 May 7;27(6):1934-1947.e5. doi: 10.1016/j.celrep.2019.04.052.

Abstract

Intestinal-type gastric cancer is preceded by premalignant lesions, including chronic atrophic gastritis and intestinal metaplasia. In this study, we constructed a single-cell atlas for 32,332 high-quality cells from gastric antral mucosa biopsies of patients spanning a cascade of gastric premalignant lesions and early gastric cancer (EGC) using single-cell RNA sequencing. We then constructed a single-cell network underlying cellular and molecular characteristics of gastric epithelial cells across different lesions. We found that gland mucous cells tended to acquire an intestinal-like stem cell phenotype during metaplasia, and we identified OR51E1 as a marker for unique endocrine cells in the early-malignant lesion. We also found that HES6 might mark the pre-goblet cell cluster, potentially aiding identification of metaplasia at the early stage. Finally, we identified a panel of EGC-specific signatures, with clinical implications for the precise diagnosis of EGC. Our study offers unparalleled insights into the human gastric cellulome in premalignant and early-malignant lesions.

Keywords: early gastric cancer; network; premalignant lesions; single-cell; stomach.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Basic Helix-Loop-Helix Transcription Factors / metabolism
  • Cell Lineage
  • Enteroendocrine Cells / metabolism
  • Enteroendocrine Cells / pathology
  • Epithelial Cells / metabolism
  • Epithelial Cells / pathology
  • Gastric Mucosa / metabolism
  • Gastric Mucosa / pathology
  • Gene Expression Regulation, Neoplastic
  • Gene Regulatory Networks*
  • Goblet Cells / metabolism
  • Humans
  • Precancerous Conditions / genetics*
  • Precancerous Conditions / pathology
  • RNA, Neoplasm / genetics
  • RNA, Neoplasm / metabolism
  • Repressor Proteins / metabolism
  • Single-Cell Analysis*
  • Stomach Neoplasms / genetics*
  • Stomach Neoplasms / pathology
  • Transcription, Genetic
  • Transcriptome / genetics*

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • HES6 protein, human
  • RNA, Neoplasm
  • Repressor Proteins