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Persistent chromatin alterations and gene expression reprogramming follow widespread DNA damage in glioblastoma

GSE300868 Homo sapiens Genome binding/occupancy profiling by high throughput sequencing 10 samples 2026/06/01 GPL24676
Summary
We introduced hundreds of CRISPR–Cas9-mediated DNA double-strand breaks (DSBs) into glioblastoma stem-like cells and tracked chromatin, transcriptional, and structural changes over time. Long after the DSBs were repaired, we found durable reprogramming of chromatin conformation and gene expression, as well as emergence of structural variants. These findings suggest that DNA damage can induce stable non-genetic alterations in cancer cells.
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