胶质母细胞瘤三维类器官建模:进展和挑战

Oxford open neuroscience Pub Date : 2023-07-06 eCollection Date: 2023-01-01 DOI:10.1093/oons/kvad008
Xin Wang, Yusha Sun, Daniel Y Zhang, Guo-Li Ming, Hongjun Song
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引用次数: 0

摘要

胶质母细胞瘤(GBM)是最具侵袭性的成人原发性脑肿瘤,几乎具有普遍的治疗耐药性和复发性。治疗的主要方法仍然是最大限度的安全手术切除,然后同时进行放射治疗和替莫唑胺化疗。尽管进行了深入的研究,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收效甚微。这种困难的部分原因是缺乏充分概括GBM瘤内和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)衍生的脑类器官的遗传操作以及与非恶性组织的生物打印或融合已成为描述GBM生物学的新培养系统。在这里,我们强调了生成GBM类器官的几种方法,并讨论了与使用细胞系和异种移植物的经典建模方法相比,使用此类类器官模型获得的见解。我们还概述了当前GBM 3D类器官的局限性,尤其是保留肿瘤微环境的困难,并讨论了目前的改进努力。最后,我们提出了类器官模型的潜在应用,以深入了解GBM的机制和治疗发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Glioblastoma modeling with 3D organoids: progress and challenges.

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.

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