Abstract
Histone deacetylases (HDAC) play a critical role in gene suppression through the recruitment of corepressor proteins to switch off gene transcription, which is activated by histone acetylation. Activated inflammatory genes are suppressed by HDAC2. Corticosteroids recruit HDAC2 to switch off inflammatory genes. HDAC2 may therefore be a target for the development of anti-inflammatory treatments, particularly in diseases where there is active corticosteroid resistance, as in chronic obstructive pulmonary disease (COPD).
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Barnes, P.J. (2011). Targeting Histone Deacetylases in Chronic Obstructive Pulmonary Disease. In: Roach, H., Bronner, F., Oreffo, R. (eds) Epigenetic Aspects of Chronic Diseases. Springer, London. https://doi.org/10.1007/978-1-84882-644-1_14
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