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[DKFZ-2022-03038]
Journal Article
Berglar, I. ; Hehlgans, S. ; Wehle, A. ; et al
CHRDL1 Regulates Stemness in Glioma Stem-like Cells.
Glioblastoma (GBM) still presents as one of the most aggressive tumours in the brain, which despite enormous research efforts, remains incurable today. As many theories evolve around the persistent recurrence of this malignancy, the assumption of a small population of cells with a stem-like phenotype remains a key driver of its infiltrative nature. [...]
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[DKFZ-2022-02533]
Journal Article
Jungwirth, G. ; Yu, T. ; Liu, F. ; et al
Pharmacological Landscape of FDA-approved Anticancer Drugs Reveals Sensitivities to Ixabepilone, Romidepsin, Omacetaxine, and Carfilzomib in Aggressive Meningiomas.
To date, there are no systemic treatment options for patients with recurrent or refractory meningioma.To identify effective drugs, we performed a large-scale drug screening using FDA-approved drugs on several meningioma cell lines. The impact of the top four compounds was assessed on cell viability, proliferation, colony formation, migration, and apoptosis. [...]
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[DKFZ-2022-02425]
Journal Article
Kebir, S. ; Ullrich, V. ; Berger, P. ; et al
A sequential targeting strategy interrupts AKT-driven subclone-mediated progression in glioblastoma.
Therapy resistance and fatal disease progression in glioblastoma are thought to result from the dynamics of intra-tumor heterogeneity. This study aimed at identifying and molecularly target tumor cells that can survive, adapt, and subclonally expand under primary therapy.To identify candidate markers and to experimentally access dynamics of subclonal progression in glioblastoma, we established a discovery cohort of paired vital cell samples obtained before and after primary therapy. [...]
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