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vorinostat and Niemann-Pick Disease, Type C

vorinostat has been researched along with Niemann-Pick Disease, Type C in 6 studies

Vorinostat: A hydroxamic acid and anilide derivative that acts as a HISTONE DEACETYLASE inhibitor. It is used in the treatment of CUTANEOUS T-CELL LYMPHOMA and SEZARY SYNDROME.
vorinostat : A dicarboxylic acid diamide comprising suberic (octanedioic) acid coupled to aniline and hydroxylamine. A histone deacetylase inhibitor, it is marketed under the name Zolinza for the treatment of cutaneous T cell lymphoma (CTCL).

Niemann-Pick Disease, Type C: An autosomal recessive lipid storage disorder that is characterized by accumulation of CHOLESTEROL and SPHINGOMYELINS in cells of the VISCERA and the CENTRAL NERVOUS SYSTEM. Type C (or C1) and type D are allelic disorders caused by mutation of the NPC1 gene, which encodes a protein that mediates intracellular cholesterol transport from LYSOSOMES. Clinical signs include hepatosplenomegaly and chronic neurological symptoms. Type D is a variant in people with a Nova Scotia ancestry.

Research Excerpts

ExcerptRelevanceReference

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's6 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Granatosky, EA1
DiPrimio, N1
Pickering, JRE1
Stevens, DC1
Perlstein, EO1
Taylor, RE1
Wang, C1
Scott, SM2
Subramanian, K3
Loguercio, S1
Zhao, P1
Hutt, DM2
Farhat, NY1
Porter, FD2
Balch, WE2
Davidson, J1
Molitor, E1
Moores, S1
Gale, SE1
Jiang, X1
Sidhu, R1
Kell, P1
Zhang, J1
Fujiwara, H1
Davidson, C1
Helquist, P2
Melancon, BJ1
Grigalunas, M1
Liu, G1
Salahi, F1
Wiest, O2
Xu, X1
Pipalia, NH2
Cruz, DL1
Holson, EB1
Schaffer, JE1
Walkley, SU1
Maxfield, FR2
Ory, DS1
Alam, MS1
Getz, M1
Haldar, K1
Mao, S1
Ralph, H1
Wehrmann, ZT1
Hulett, TW1
Huegel, KL1
Vaughan, KT1
Goodson, H1

Other Studies

6 other studies available for vorinostat and Niemann-Pick Disease, Type C

ArticleYear
GEX1A, a Polyketide from Streptomyces chromofuscus, Corrects the Cellular Defects Associated with Niemann-Pick Type C1 in Human Fibroblasts.
    Journal of natural products, 2018, 09-28, Volume: 81, Issue:9

    Topics: Cell Line; Cholesterol; Fatty Alcohols; Fibroblasts; Humans; Molecular Structure; Niemann-Pick Disea

2018
Quantitating the epigenetic transformation contributing to cholesterol homeostasis using Gaussian process.
    Nature communications, 2019, 11-07, Volume: 10, Issue:1

    Topics: Cell Line, Tumor; Cholesterol; Endosomes; Epigenesis, Genetic; Epigenomics; Fibroblasts; HeLa Cells;

2019
2-Hydroxypropyl-β-cyclodextrin is the active component in a triple combination formulation for treatment of Niemann-Pick C1 disease.
    Biochimica et biophysica acta. Molecular and cell biology of lipids, 2019, Volume: 1864, Issue:10

    Topics: 2-Hydroxypropyl-beta-cyclodextrin; Animals; Cells, Cultured; Drug Combinations; Histone Deacetylase

2019
Chronic administration of an HDAC inhibitor treats both neurological and systemic Niemann-Pick type C disease in a mouse model.
    Science translational medicine, 2016, Feb-17, Volume: 8, Issue:326

    Topics: 2-Hydroxypropyl-beta-cyclodextrin; Animals; beta-Cyclodextrins; Blood-Brain Barrier; Disease Models,

2016
Histone deacetylase inhibitors correct the cholesterol storage defect in most Niemann-Pick C1 mutant cells.
    Journal of lipid research, 2017, Volume: 58, Issue:4

    Topics: Carrier Proteins; Cell Line; Cholesterol; Endoplasmic Reticulum-Associated Degradation; Endosomes; F

2017
Quantitative comparison of the efficacy of various compounds in lowering intracellular cholesterol levels in Niemann-Pick type C fibroblasts.
    PloS one, 2012, Volume: 7, Issue:10

    Topics: Azacitidine; beta-Cyclodextrins; Cells, Cultured; Child; Child, Preschool; Chloroquine; Chlorpromazi

2012