Abstract:The contribution of deregulated chromatin architecture, including topologically associated domains (TADS), to cancer progression remains ambiguous. CTCF is a central regulator of higher-order chromatin structure that undergoes copy number loss in over half of all breast cancers, but the impact of this defect on epigenetic programming and chromatin architecture remains unclear. We find that under physiological conditions, CTCF organizes sub-TADs to limit the expression of oncogenic pathways, including PI3K and … Show more
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