Department of Neuroscience, University of Texas Southwestern Medical Center at Dallas, Dallas, Texas 75390-9111, USA.
J Biol Chem. 2011 May 6;286(18):16101-8. doi: 10.1074/jbc.M110.193433. Epub 2011 Mar 23.
Progranulin (GRN) haploinsufficiency is a frequent cause of familial frontotemporal dementia, a currently untreatable progressive neurodegenerative disease. By chemical library screening, we identified suberoylanilide hydroxamic acid (SAHA), a Food and Drug Administration-approved histone deacetylase inhibitor, as an enhancer of GRN expression. SAHA dose-dependently increased GRN mRNA and protein levels in cultured cells and restored near-normal GRN expression in haploinsufficient cells from human subjects. Although elevation of secreted progranulin levels through a post-transcriptional mechanism has recently been reported, this is, to the best of our knowledge, the first report of a small molecule enhancer of progranulin transcription. SAHA has demonstrated therapeutic potential in other neurodegenerative diseases and thus holds promise as a first generation drug for the prevention and treatment of frontotemporal dementia.
颗粒蛋白前体 (GRN) 单倍体不足是家族性额颞叶痴呆的常见原因,这是一种目前无法治愈的进行性神经退行性疾病。通过化学文库筛选,我们发现了琥珀酰亚胺基草酰苯胺(suberoylanilide hydroxamic acid,SAHA),一种获得美国食品和药物管理局批准的组蛋白去乙酰化酶抑制剂,是 GRN 表达的增强剂。SAHA 可剂量依赖性地增加培养细胞中的 GRN mRNA 和蛋白水平,并恢复来自人类受试者的单倍体不足细胞中近乎正常的 GRN 表达。尽管最近有报道称通过转录后机制升高分泌性颗粒蛋白水平,但据我们所知,这是第一个报道颗粒蛋白转录的小分子增强剂。SAHA 在其他神经退行性疾病中已显示出治疗潜力,因此有望成为预防和治疗额颞叶痴呆的第一代药物。