Li Weiqing, Zhang Tai
Institute of Burn Research, State Key Laboratory of Trauma, Burns and Combined Injury, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing, China.
Peking University Traditional Chinese Medicine Clinical Medical School (Xiyuan), Peking University Health Science Center, Beijing, China.
Front Cell Dev Biol. 2025 Jul 2;13:1620756. doi: 10.3389/fcell.2025.1620756. eCollection 2025.
Gastric cancer remains a significant global health challenge, representing the fifth most commonly diagnosed cancer and the fourth leading cause of cancer-related mortality worldwide. Understanding the pathogenesis of precancerous lesions is crucial for developing effective prevention and treatment strategies. This review provides a comprehensive analysis of animal models for gastric precancerous lesions, categorizing them into infection models, chemical carcinogen or diet-induced models, multifactorial induction models, chemical injury models, and genetically engineered mouse models. We evaluate the advantages and limitations of each model type, with particular focus on their ability to recapitulate the Correa cascade of human gastric carcinogenesis. While felis infection in C57BL/6 mice most closely mirrors the progression from chronic gastritis through metaplasia to dysplasia, these models primarily produce spasmolytic polypeptide-expressing metaplasia rather than true intestinal metaplasia, limiting translational relevance. Chemical carcinogen models reliably produce tumors but often bypass intermediate precancerous stages. Recent advances in genetic engineering, particularly stomach-specific inducible Cre recombinase systems targeting gastric progenitor cells, have yielded models that faithfully reproduce the spectrum of human gastric cancer subtypes with features of metastatic disease. We highlight the importance of standardized histopathological evaluation methodologies and discuss future research directions, including integration of advanced technologies such as single-cell RNA sequencing with existing animal models, development of organoid models, and investigation of interactions among genetic predisposition, infection, and environmental factors. This review provides a valuable reference for researchers investigating gastric precancerous lesions and offers insights for the development of more effective prevention and treatment strategies.
胃癌仍然是一项重大的全球健康挑战,是全球第五大最常被诊断出的癌症以及第四大癌症相关死亡原因。了解癌前病变的发病机制对于制定有效的预防和治疗策略至关重要。本综述对胃癌前病变的动物模型进行了全面分析,将它们分为感染模型、化学致癌物或饮食诱导模型、多因素诱导模型、化学损伤模型和基因工程小鼠模型。我们评估了每种模型类型的优缺点,特别关注它们重现人类胃癌发生的科雷亚级联反应的能力。虽然C57BL/6小鼠中的幽门螺杆菌感染最能反映从慢性胃炎到化生再到发育异常的进展,但这些模型主要产生表达解痉多肽的化生而非真正的肠化生,限制了转化相关性。化学致癌物模型能可靠地产生肿瘤,但往往绕过中间癌前阶段。基因工程的最新进展,特别是针对胃祖细胞的胃特异性诱导型Cre重组酶系统,产生了能忠实地重现具有转移性疾病特征的人类胃癌亚型谱的模型。我们强调标准化组织病理学评估方法的重要性,并讨论未来的研究方向,包括将单细胞RNA测序等先进技术与现有动物模型相结合、类器官模型的开发以及对遗传易感性、感染和环境因素之间相互作用的研究。本综述为研究胃癌前病变的研究人员提供了有价值的参考,并为开发更有效的预防和治疗策略提供了见解。