INSM1 governs a neuronal progenitor state that drives glioblastoma in a human stem cell model
Issued Date
2026-12-01
Resource Type
eISSN
20411723
Scopus ID
2-s2.0-105026372559
Pubmed ID
41354838
Journal Title
Nature Communications
Volume
17
Issue
1
Rights Holder(s)
SCOPUS
Bibliographic Citation
Nature Communications Vol.17 No.1 (2026)
Suggested Citation
DeSouza P.A., Ishahak M., Qu X., McCornack C., Annamalai D., Mao D.D., Vangipurapu R., Fu Y., Vessoni A.T., Cleary R.T., Han R.H., Augsornworawat P., Woodiwiss T., Agovino D., Sizemore B., Kline J., Borhani-Haghighi M., Chen H., Pugazenthi S., Yano H., Wang T., Batista L.F.Z., Millman J.R., Kim A.H. INSM1 governs a neuronal progenitor state that drives glioblastoma in a human stem cell model. Nature Communications Vol.17 No.1 (2026). doi:10.1038/s41467-025-66371-x Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/114541
Title
INSM1 governs a neuronal progenitor state that drives glioblastoma in a human stem cell model
Corresponding Author(s)
Other Contributor(s)
Abstract
Glioblastoma is a lethal brain cancer marked by functional plasticity driven by tumor cell-intrinsic mutations and their interplay with developmental programs. To investigate how canonical glioblastoma mutations promote functional plasticity, we have developed an isogenic human neural stem cell (NSC) model of glioblastoma by sequential addition of TERT promoter, TP53, and PDGFRA point mutations. TP53 loss-of-function increases TERT expression during serial mutagenesis, but only triple mutant NSCs reliably form lethal brain tumors in vivo that recapitulate glioblastoma. Tumor cell evolution triggers stress-related metabolic changes and transitions toward a neuronal progenitor network driven by transcription factor INSM1. INSM1 is highly expressed in human glioblastoma tumors and, during cortical development, in intermediate progenitor cells, which give rise to neurons. Remarkably, INSM1 knockdown in triple mutant NSCs and primary glioblastoma cells disrupts oncogenic gene expression and function and inhibits the in vivo tumorigenicity of triple mutant NSCs, highlighting the functional importance of an intermediate progenitor cell-like cell state in glioblastoma pathogenesis.