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Dissecting the differentiation origins of intestinal metaplasia and early intestinal-type gastric cancer in gastric antrum by single-cell RNA profiling
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  • Published: 10 March 2026

Dissecting the differentiation origins of intestinal metaplasia and early intestinal-type gastric cancer in gastric antrum by single-cell RNA profiling

  • Honghao Yin1,2,3,4 na1,
  • Huanyu Zhang1,2,3 na1,
  • Shuwen Zheng1,2,3 na1,
  • Rui Guo1,2,3,
  • Jing Wen1,2,3,
  • Mengyuan Liu5,
  • Aicun Li1,2,3,
  • Mingfang Zhao4,
  • Yuan Yuan1,2,3 &
  • …
  • Yuehua Gong1,2,3 

npj Precision Oncology , Article number:  (2026) Cite this article

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We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply.

Subjects

  • Biomarkers
  • Computational biology and bioinformatics
  • Diseases
  • Oncology
  • Pathogenesis

Abstract

Intestinal-type gastric cancer (IGC) is associated with a multi-step carcinogenic process, comprising non-atrophic gastritis, chronic atrophic gastritis, intestinal metaplasia, and gastric dysplasia. The risk of developing IGC gradually increases as the disease progresses. However, the origin of cell differentiation and its carcinogenic potential in different stages of gastric disease remains poorly understood. To address this issue, we analyzed the differentiation trajectory of epithelial cells in different disease stages from gastric antrum biopsies in patients with precancerous lesions and early GC using single-cell sequencing data. Our findings revealed that progenitor cells (PCs) act as the ancestors of antral gland mucous cells (GMCs) and pit mucous cells (PMCs) in the NAG/CAG stage. In the IM stage, GMCs, as well as PCs, may acquire the ability to become intestinal-like stem cell phenotypes, eventually differentiating into mature enterocyte cells. Secretory progenitor cells may differentiate into pre-secretory cells and goblet cells. In the early IGC stage, KIAA0101+PRAP1+ PCs may be the potential origin of early IGC. These findings provide valuable insights for further research into the molecular mechanisms underlying the development of IGC and may contribute to the development of novel prevention and treatment strategies.

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Data availability

All data included in this study are available upon request by contacting the corresponding author. Additionally, publicly available datasets were analyzed, which can be accessed at GEO: GSE134520, GSE251950, GSE60662, GSE130823, and GSE191275.

Code availability

The code used for this study is not publicly available but may be made available to qualified researchers on reasonable request from the corresponding author.

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Acknowledgements

This work was supported by Noncommunicable Chronic Diseases-National Science and Technology Major Project (No. 2023ZD0501400), the National Key R&D Program of China (Grant No. 2023YFB4705700), and the Education Department project of Liaoning Province (Nos. LJ212410159002 and LJKMZ20221142). Figure 7 was created with BioRender (https://biorender.com/; accessed on January 27, 2026).

Author information

Author notes
  1. These authors contributed equally: Honghao Yin, Huanyu Zhang, Shuwen Zheng.

Authors and Affiliations

  1. Tumor Etiology and Screening Department of Cancer Institute and General Surgery, the First Hospital of China Medical University, Shenyang, China

    Honghao Yin, Huanyu Zhang, Shuwen Zheng, Rui Guo, Jing Wen, Aicun Li, Yuan Yuan & Yuehua Gong

  2. Key Laboratory of Cancer Etiology and Prevention in Liaoning Education Department, the First Hospital of China Medical University, Shenyang, China

    Honghao Yin, Huanyu Zhang, Shuwen Zheng, Rui Guo, Jing Wen, Aicun Li, Yuan Yuan & Yuehua Gong

  3. Key Laboratory of GI Cancer Etiology and Prevention in Liaoning Province, the First Hospital of China Medical University, Shenyang, China

    Honghao Yin, Huanyu Zhang, Shuwen Zheng, Rui Guo, Jing Wen, Aicun Li, Yuan Yuan & Yuehua Gong

  4. Department of Medical Oncology, the First Hospital of China Medical University, Shenyang, China

    Honghao Yin & Mingfang Zhao

  5. Department of Gastroenterology, the First Hospital of China Medical University, Shenyang, China

    Mengyuan Liu

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Contributions

Y.-Y., Y.H.-G., and H.H.-Y. conceived the study. H.H.-Y., H.Y.-Z., S.W.-Z., Y.H.-G., and Y.-Y. drafted the manuscript and performed the analysis. H.H.-Y., H.Y.-Z., M.Y.-L., and R.G. conducted the literature search and data collection. H.H.-Y., S.W.-Z., and A.C.-L. were contributed to the IHC staining and IF experiments. H.H.-Y., S.W.-Z., J.-W., and M.F.-Z. contributed to data interpretation. H.H.-Y., M.Y.-L., and M.F.-Z. were involved in the underlying computer architecture. All authors have reviewed and approved the final manuscript.

Corresponding authors

Correspondence to Mingfang Zhao, Yuan Yuan or Yuehua Gong.

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Yin, H., Zhang, H., Zheng, S. et al. Dissecting the differentiation origins of intestinal metaplasia and early intestinal-type gastric cancer in gastric antrum by single-cell RNA profiling. npj Precis. Onc. (2026). https://doi.org/10.1038/s41698-026-01355-8

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  • Received: 23 April 2025

  • Accepted: 23 February 2026

  • Published: 10 March 2026

  • DOI: https://doi.org/10.1038/s41698-026-01355-8

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