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- W2292508736 abstract "The pathogenesis of autoimmune and neurodegenerative diseases involves overexpression of inducible subunits of the immunoproteasome. However, the clinical application of inhibitors to inducible subunits of the immunoproteasome has been limited due to systemic toxicity. Here, we designed siRNAs that efficiently silence LMP2, LMP7 and MECL-1 gene expression. Inducible subunits of the immunoproteasome are complex siRNA targets because they have a long half-life; therefore, we introduced 2′-O-methyl modifications into nuclease-sensitive sites. This led to 90–95% silencing efficiency and prolonged silencing, eliminating the need for multiple transfections. Furthermore, we showed that in the absence of transfection reagent, siRNAs with lipophilic residues were able to penetrate cells more effectively and decrease the expression of inducible immunoproteasome subunits by 35% after 5 days. These results show that siRNA targeted to inducible immunoproteasome subunits have great potential for the development of novel therapeutics for autoimmune and neurodegenerative diseases." @default.
- W2292508736 created "2016-06-24" @default.
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- W2292508736 date "2016-06-01" @default.
- W2292508736 modified "2023-10-14" @default.
- W2292508736 title "Modified siRNA effectively silence inducible immunoproteasome subunits in NSO cells" @default.
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- W2292508736 doi "https://doi.org/10.1016/j.biochi.2016.02.015" @default.
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