Therapeutic potential of histone deacetylase inhibitor for treatment of Niemann-Pick type C1 disease

Abstract

Background Niemann-Pick type C (NPC) is a rare, autosomal recessive neurodegenerative lysosomal storage disorder (LSD) caused due to mutation in either npc1 or npc2 genes. However, 95% of the reported cases are caused due to mutation in npc1 gene and only 5% due to the mutation in npc2 gene. Mutations in either of these two genes results in similar phenotype such that there is an abnormal accumulation of unesterified cholesterol and glycosphingolipids in late endosomes/ lysosomes (LE/Ly) of many cell types. NPC1 is a multi-spanning transmembrane protein localized in limiting membrane of LE/Ly whereas NPC2 is soluble cholesterol binding protein localized in the lumen of LE/Ly. There are no therapeutic options to treat the disease and the children born with this defect die before the age of 20 years. Miglustat, a drug used to treat Gaucher disease has been reported to stabilize NPC patients and has also been approved for treating NPC patients in Europe. Infusion of very high dose of chemical chaperone like 2-hydroxypropyl-b-cyclodextrin (HPBCD) several times a week has also been shown to reduce the cholesterol load in peripheral tissues. Unfortunately, the blood brain barrier (BBB) cross over capability of HPCD is very poor and hence requires intrathecal CNS injections.