Synthetic lethality through Gsk3β inhibition in glioma stem cells via the WNT-WWC1-YAP axis Journal Article


Authors: Ren, F.; Yi, Y.; Lu, T.; Liu, X.; Cui, G.; Huang, S.; Parada, L. F.; Chen, J.
Article Title: Synthetic lethality through Gsk3β inhibition in glioma stem cells via the WNT-WWC1-YAP axis
Abstract: Glioblastoma (GBM) is an aggressive brain tumor driven by glioma stem cells (GSCs), which contribute to tumor growth and therapeutic resistance. This study investigates the effects of Gsk3β inhibition on GSC viability, focusing on the role of the canonical WNT signaling pathway. We found that Gsk3β inhibition activates the WNT pathway, leading to upregulation of Wwc1, which downregulates Yap via Lats1 phosphorylation. This reduces GSC proliferation, self-renewal, and enhances chemosensitivity. Analysis of clinical datasets revealed that WNT pathway activation correlates with improved prognosis in proneural gliomas, particularly in IDH1-mutated tumors. Our findings suggest that targeting the WNT-WWC1-YAP axis, particularly through Gsk3β inhibition, could induce synthetic lethality in GSCs and provide a promising therapeutic strategy for gliomas. These results highlight the potential of exploiting WNT-induced synthetic lethality as a novel approach for glioma treatment. © The Author(s), under exclusive licence to Springer Nature Limited 2025.
Journal Title: Oncogene
ISSN: 09509232
Publisher: The Author(s), Under Exclusive Licence To Springer Nature Limited 2025  
Date Published: 2025-01-01
Start Page: 6740
Language: English
DOI: 10.1038/s41388-025-03418-9
PROVIDER: scopus
DOI/URL:
Notes: Article -- Source: Scopus
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