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REVIEW article

Front. Oncol.

Sec. Gastrointestinal Cancers: Gastric and Esophageal Cancers

Advances in Modeling Gastric Intestinal Metaplasia: A Comprehensive Review of Experimental Models and Mechanistic Insights

Provisionally accepted
  • Capital Medical University Affiliated Beijing Friendship Hospital, Beijing, China

The final, formatted version of the article will be published soon.

Epithelial cells within the gastric corpus mucosa exhibit a dynamic response to injury, characterized by alterations in gene transcription, cellular phenotype, and tissue organization, collectively termed metaplasia. Among these changes, gastric intestinal metaplasia (GIM) represents one of the most prevalent precancerous lesions associated with intestinal-type gastric cancer (GC). This pathological progression typically evolves through a sequence of stages: chronic atrophic gastritis, intestinal metaplasia, atypical hyperplasia, and ultimately, GC. A deeper understanding of GIM is crucial for advancing diagnostic and therapeutic strategies in GC management. Despite its clinical significance, progress in elucidating the underlying mechanisms of GIM has been limited, primarily due to the lack of reliable and reproducible animal models that accurately recapitulate this condition. This review systematically examines the existing mouse, rat, and organoid models utilized for GIM research, providing critical insights into various methodological approaches and potential mechanisms. Specifically, we investigate five pivotal aspects of pyloric metaplasia and GIM: Helicobacter pylori infection, bile acid induction, chemical agent interventions, transgenic technologies, and gastric organoids. Through this comprehensive analysis, we aim to establish a robust foundation for future research initiatives focused on unraveling the molecular mechanisms driving GIM development and formulating effective prevention and treatment strategies.

Keywords: Gastric intestinal metaplasia, Animal Models, Helicobacter pylori, Bile acid, gastricorganoids

Received: 11 Jul 2025; Accepted: 03 Nov 2025.

Copyright: © 2025 Liu, Yang, Zhang and Sun. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Xiujing Sun, sunxiujing@ccmu.edu.cn

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