Title: |
Advancing Glioblastoma Research with Innovative Brain Organoid-Based Models. |
Authors: |
Correia, Cátia D.1,2 (AUTHOR) a57384@ualg.pt, Calado, Sofia M.1,3 (AUTHOR) sofia.am.calado@uac.pt, Matos, Alexandra1 (AUTHOR) macampinho@ualg.pt, Esteves, Filipa1,2 (AUTHOR), De Sousa-Coelho, Ana Luísa1,4 (AUTHOR), Campinho, Marco A.1,2 (AUTHOR), Fernandes, Mónica T.1,4 (AUTHOR) mafernandes@ualg.pt |
Source: |
Cells (2073-4409). Feb2025, Vol. 14 Issue 4, p292. 30p. |
Subject Terms: |
*DRUG discovery, *HUMAN stem cells, *GENETIC techniques, *GLIOBLASTOMA multiforme, *TUMOR microenvironment |
Abstract: |
Glioblastoma (GBM) is a relatively rare but highly aggressive form of brain cancer characterized by rapid growth, invasiveness, and resistance to standard therapies. Despite significant progress in understanding its molecular and cellular mechanisms, GBM remains one of the most challenging cancers to treat due to its high heterogeneity and complex tumor microenvironment. To address these obstacles, researchers have employed a range of models, including in vitro cell cultures and in vivo animal models, but these often fail to replicate the complexity of GBM. As a result, there has been a growing focus on refining these models by incorporating human-origin cells, along with advanced genetic techniques and stem cell-based bioengineering approaches. In this context, a variety of GBM models based on brain organoids were developed and confirmed to be clinically relevant and are contributing to the advancement of GBM research at the preclinical level. This review explores the preparation and use of brain organoid-based models to deepen our understanding of GBM biology and to explore novel therapeutic approaches. These innovative models hold significant promise for improving our ability to study this deadly cancer and for advancing the development of more effective treatments. [ABSTRACT FROM AUTHOR] |
|
Copyright of Cells (2073-4409) is the property of MDPI and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) |
Database: |
Academic Search Complete |