Wang Xin, Sun Yusha, Zhang Daniel Y, Ming Guo-Li, Song Hongjun
Department of Neuroscience and Mahoney Institute for Neurosciences, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Neuroscience Graduate Group, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Oxf Open Neurosci. 2023 Jul 6;2:kvad008. doi: 10.1093/oons/kvad008. eCollection 2023.
Glioblastoma (GBM) is the most aggressive adult primary brain tumor with nearly universal treatment resistance and recurrence. The mainstay of therapy remains maximal safe surgical resection followed by concurrent radiation therapy and temozolomide chemotherapy. Despite intensive investigation, alternative treatment options, such as immunotherapy or targeted molecular therapy, have yielded limited success to achieve long-term remission. This difficulty is partly due to the lack of pre-clinical models that fully recapitulate the intratumoral and intertumoral heterogeneity of GBM and the complex tumor microenvironment. Recently, GBM 3D organoids originating from resected patient tumors, genetic manipulation of induced pluripotent stem cell (iPSC)-derived brain organoids and bio-printing or fusion with non-malignant tissues have emerged as novel culture systems to portray the biology of GBM. Here, we highlight several methodologies for generating GBM organoids and discuss insights gained using such organoid models compared to classic modeling approaches using cell lines and xenografts. We also outline limitations of current GBM 3D organoids, most notably the difficulty retaining the tumor microenvironment, and discuss current efforts for improvements. Finally, we propose potential applications of organoid models for a deeper mechanistic understanding of GBM and therapeutic development.
胶质母细胞瘤(GBM)是最具侵袭性的成人原发性脑肿瘤,几乎普遍存在治疗抵抗和复发情况。治疗的主要手段仍然是最大限度的安全手术切除,随后进行同步放疗和替莫唑胺化疗。尽管进行了深入研究,但免疫疗法或靶向分子疗法等替代治疗方案在实现长期缓解方面取得的成功有限。造成这种困难的部分原因是缺乏能够完全重现GBM肿瘤内和肿瘤间异质性以及复杂肿瘤微环境的临床前模型。最近,源自切除的患者肿瘤的GBM 3D类器官、诱导多能干细胞(iPSC)衍生的脑类器官的基因操作以及与非恶性组织的生物打印或融合已成为描绘GBM生物学特性的新型培养系统。在这里,我们重点介绍了几种生成GBM类器官的方法,并讨论了与使用细胞系和异种移植的经典建模方法相比,使用此类类器官模型所获得的见解。我们还概述了当前GBM 3D类器官的局限性,最显著的是难以保留肿瘤微环境,并讨论了当前的改进努力。最后,我们提出了类器官模型在更深入理解GBM机制和治疗开发方面的潜在应用。