Bhat Nadeem, Al-Mathkour Marwah, Maacha Selma, Lu Heng, El-Rifai Wael, Ballout Farah
Department of Surgery, Miller School of Medicine, University of Miami, Miami, FL, United States.
Department of Veterans Affairs, Miami Healthcare System, Miami, FL, United States.
Front Mol Biosci. 2024 Nov 12;11:1440670. doi: 10.3389/fmolb.2024.1440670. eCollection 2024.
Esophageal adenocarcinoma (EAC) is a subtype of esophageal cancer with significant morbidity and mortality rates worldwide. Despite advancements in tumor models, the underlying cellular and molecular mechanisms driving EAC pathogenesis are still poorly understood. Therefore, gaining insights into these mechanisms is crucial for improving patient outcomes. Researchers have developed various models to better understand EAC and evaluate clinical management strategies. However, no single model fully recapitulates the complexity of EAC. Emerging technologies, such as patient-derived organoids and immune-competent mouse models, hold promise for personalized EAC research and drug development. In this review, we shed light on the various models for studying EAC and discuss their advantages and limitations.
食管腺癌(EAC)是一种食管癌亚型,在全球范围内具有较高的发病率和死亡率。尽管肿瘤模型有所进展,但驱动EAC发病机制的潜在细胞和分子机制仍知之甚少。因此,深入了解这些机制对于改善患者预后至关重要。研究人员已开发出各种模型,以更好地理解EAC并评估临床管理策略。然而,没有一种单一模型能完全概括EAC的复杂性。新兴技术,如患者来源的类器官和具有免疫活性的小鼠模型,有望用于个性化的EAC研究和药物开发。在本综述中,我们阐明了用于研究EAC的各种模型,并讨论了它们的优缺点。