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ING2 encodes a nuclear protein that binds to methylated histones (especially H3K4me3) via a plant homeodomain (PHD) zinc finger and is part of the mSin3A/HDAC complex involved in chromatin remodeling and gene repression. It functions primarily as a tumor suppressor by regulating transcription, apoptosis, cellular senescence, and DNA repair. ING2 modulates p53 function, is subject to dynamic regulation via phosphorylation and ubiquitination, and its loss or mislocalization is associated with tumorigenesis. ING2 is implicated in the development and progression of multiple cancers, including colorectal and gynecological cancers, and is being explored as a marker for tumor progression and as a potential therapeutic target through epigenetic and chromatin-targeting strategies.
Drugs may alter ING2 function by affecting HDAC/mSin3A complex activity or by targeting chromatin remodeling, though no specific ING2-targeted drug mechanism is validated yet.
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