28/03/2026
PUBLISHED :- Original Research Article
Title : Targeting glioblastoma through chromatin remodeling: epigenetic insights into actionable molecular pathways.
*Corresponding author: Tshetiz Dahal
DOI: https;//doi;10.18231/j.sajhp.57585.1774594650
© 2026 The Author(s), Published by Innovative Publications.
Journal : Southeast Asian Journal of Case Report and Review ISSN (Online): 2319-1090. Publisher: IP Innovative Publication
Volume : 2026;9(1): Pages : 10-20
Link : https://sajhp.com/archive/volume/9/issue/1/article/26489/pdf
Journal homepage: https://www.sajcrr.com/
ABSTRACT :
Background: Glioblastoma is the most common and highly aggressive primary brain tumor in adults, characterized by rapid progression and dismal patient
survival. Its profound intratumoral heterogeneity, driven predominantly by epigenetic dysregulation, presents major challenges to effective therapeutic
development. Understanding the chromatin remodeling programs that distinguish glioblastoma stem cells (GSCs) from normal neural stem cells (NSCs) is essential for identifying actionable molecular vulnerabilities.
Materials and Methods: To investigate epigenetically driven regulatory mechanisms underlying glioblastoma pathogenesis, we employed SYNGN, a specialised syngeneic experimental framework enabling direct comparison between GSCs and NSCs derived from expanded potential stem cells (EPSCs). This platform allowed high-resolution profiling of chromatin architecture, transcriptional programs, and signaling pathway alterations unique to GSC populations.
Results: Our analysis revealed that chromatin remodeling profoundly influences the transcriptional landscape of glioblastoma stem cells, regulating key
oncogenic genes and signaling cascades responsible for tumor initiation, maintenance, and progression. Comparative profiling between GSCs and NSCs
identified distinct epigenetically modulated pathways that are selectively activated in malignant cells. Notably, we discovered previously unrecognised, patient-specific epigenetically regulated therapeutic targets, including SMOX and GABBR2, which exhibit strong potential as precision drug targets in glioblastoma.
Conclusion: This study highlights the pivotal role of epigenetic modulation in shaping the transcriptional and functional identity of glioblastoma stem cells.
By leveraging the SYNGN framework, we uncover novel, patient-specific vulnerabilities—most prominently SMOX and GABBR2—that hold promise for
targeted therapeutic development. These findings underscore the importance of chromatin remodeling–based analyses in understanding glioblastoma biology
and advancing personalised treatment strategies for this highly lethal malignancy.
Citation : Dahal T. Targeting glioblastoma through
chromatin remodeling: epigenetic insights into actionable molecular pathways. South Asian J Health Prof. 2026;9(1):10-20.
© 2026 Southeast Asian Journal of Case Report and Review
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