TY - JOUR
T1 - Suberoylanilide hydroxamic acid (vorinostat) up-regulates progranulin transcription
T2 - Rational therapeutic approach to frontotemporal dementia
AU - Cenik, Basar
AU - Sephton, Chantelle F.
AU - Dewey, Colleen M.
AU - Xian, Xunde
AU - Wei, Shuguang
AU - Yu, Kimberley
AU - Niu, Wenze
AU - Coppola, Giovanni
AU - Coughlin, Sarah E.
AU - Lee, Suzee E.
AU - Dries, Daniel R.
AU - Almeida, Sandra
AU - Geschwind, Daniel H.
AU - Gao, Fen Biao
AU - Miller, Bruce L.
AU - Farese, Robert V.
AU - Posner, Bruce A.
AU - Yu, Gang
AU - Herz, Joachim
PY - 2011/5/6
Y1 - 2011/5/6
N2 - 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.
AB - 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.
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U2 - 10.1074/jbc.M110.193433
DO - 10.1074/jbc.M110.193433
M3 - Article
C2 - 21454553
AN - SCOPUS:79955534069
SN - 0021-9258
VL - 286
SP - 16101
EP - 16108
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 18
ER -