Hettiarachchi Piyanka, Park Taeju
Department of Pediatrics, Children's Mercy Research Institute, Children's Mercy Kansas City, Kansas City, MO 64108, USA.
Department of Pediatrics, University of Missouri-Kansas City School of Medicine, Kansas City, MO 64108, USA.
Cancers (Basel). 2025 Aug 26;17(17):2776. doi: 10.3390/cancers17172776.
Glioblastoma is an aggressive and prevalent form of brain cancer characterized by rapid tumor cell migration and invasion into surrounding healthy tissues, making it resistant to conventional treatments. Despite advances in therapeutic approaches, patient prognosis remains poor, with a median survival of approximately 15 months. Tumor cell infiltration along perivascular spaces and white matter tracts is a major driver of recurrence, underscoring the need for experimental models that accurately capture these invasive behaviors. Animal models remain indispensable for this purpose, offering insights that cannot be fully replicated in vitro. This review focuses on applying animal models to elucidate the mechanisms underlying glioblastoma cell migration and invasion, which remain critical to improving therapeutic outcomes. By comparing the advantages of animal models with in vitro systems, we highlight the unique insights animal models provide, particularly in capturing the intricate dynamics of tumor cell motility. In particular, patient-derived xenograft (PDX) models preserve patient-specific heterogeneity and invasion patterns, such as white matter tract and perivascular infiltration, enabling clinically relevant drug testing. Zebrafish xenografts provide real-time, high-resolution visualization of tumor-vascular interactions, facilitating rapid assessment of invasion dynamics and early-stage drug screening. Genetically engineered models (GEM) allow precise discrimination of how defined genetic alterations drive specific invasive routes in the brain. Furthermore, we explore the use of advanced imaging techniques in these models to monitor tumor progression in real time. Moreover, we discuss the major drawbacks of these animal models, such as incomplete immune components and tumor microenvironment recapitulation. Ultimately, animal models are essential for bridging the gap between basic research and clinical application, offering a powerful platform for developing targeted strategies to combat glioblastoma's relentless progression.
胶质母细胞瘤是一种侵袭性且常见的脑癌形式,其特征在于肿瘤细胞快速迁移并侵入周围健康组织,使其对传统治疗产生抗性。尽管治疗方法有所进步,但患者预后仍然很差,中位生存期约为15个月。肿瘤细胞沿血管周围间隙和白质束浸润是复发的主要驱动因素,这突出了需要能够准确捕捉这些侵袭行为的实验模型。动物模型在此目的上仍然不可或缺,能提供无法在体外完全复制的见解。本综述重点关注应用动物模型来阐明胶质母细胞瘤细胞迁移和侵袭的潜在机制,这对于改善治疗结果仍然至关重要。通过比较动物模型与体外系统的优势,我们突出了动物模型提供的独特见解,特别是在捕捉肿瘤细胞运动的复杂动态方面。特别是,患者来源的异种移植(PDX)模型保留了患者特异性的异质性和侵袭模式,如白质束和血管周围浸润,从而实现临床相关的药物测试。斑马鱼异种移植提供了肿瘤 - 血管相互作用的实时、高分辨率可视化,便于快速评估侵袭动态和早期药物筛选。基因工程模型(GEM)能够精确区分特定的基因改变如何驱动大脑中特定的侵袭途径。此外,我们探讨了在这些模型中使用先进成像技术来实时监测肿瘤进展。此外,我们讨论了这些动物模型的主要缺点,如免疫成分不完整和肿瘤微环境重现性不足。最终,动物模型对于弥合基础研究与临床应用之间的差距至关重要,为制定针对性策略以对抗胶质母细胞瘤的无情进展提供了一个强大的平台。