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EZH2 shRNA is a short hairpin RNA designed to silence the expression of Enhancer of Zeste Homolog 2 (EZH2), a histone methyltransferase that serves as the catalytic subunit of the Polycomb Repressive Complex 2 (PRC2). By targeting EZH2 mRNA for degradation via the RNA interference (RNAi) pathway, EZH2 shRNA reduces the levels of H3K27me3 (trimethylation of histone H3 lysine 27), thereby modulating gene expression. In research settings, it is utilized to investigate the role of EZH2 in various pathologies, including cancer and cardiovascular diseases like atherosclerosis. Specifically, it has been used to demonstrate that EZH2 knockdown can attenuate endothelial-to-mesenchymal transition (EndMT) in diabetic models, suggesting its potential as a therapeutic target for cardiovascular complications in diabetes.
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