Animal models for Niemann-Pick type C: implications for drug discovery & development

被引:27
作者
Fog, Cathrine K. [1 ]
Kirkegaar, Thomas [1 ]
机构
[1] Orphazyme AS, Copenhagen, Denmark
关键词
Animal model; cholesterol; drug development; glycosphingolipids; lysosomal storage diseases; lysosomes; Niemann-Pick type C; NPC; NPC1; NPC2; sphingolipids; DISEASE; IDENTIFICATION; MOUSE; GLYCOSPHINGOLIPIDS; NEURODEGENERATION; ACCUMULATION; BIOMARKERS; MIGLUSTAT; SURVIVAL; MUTATION;
D O I
10.1080/17460441.2019.1588882
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Niemann-Pick type C (NPC) is a neurovisceral, progressively detrimental lysosomal storage disease with very limited therapeutic options and no approved treatment available in the US. Despite its rarity, NPC has seen increased drug developmental efforts over the past decade, culminating in the completion of two potential registration trials in 2018. Areas covered: This review highlights the many available animal models that have been developed in the field and briefly covers classical and new cell technologies. This review provides a high-level evaluation and prioritization of the various models with regard to efficient and clinically translatable drug development, and briefly discusses the relevant developments and opportunities pertaining to this. Expert opinion: With a number of in vitro and in vivo models available, and with having several drugs, all with various mechanisms of action, either approved or in late stage development, the NPC field is in an exciting time. One of the challenges for researchers and developers will be the ability to make use of the lessons learnt from existing late-stage programs as well as the incorporation not only of the opportunities but also the limitations of the many models into successful drug discovery and translational development programs.
引用
收藏
页码:499 / 509
页数:11
相关论文
共 117 条
[21]  
GELSTHORPE ME, 2013, INTERNET, V283, P8229, DOI DOI 10.1074/JBC.M708735200
[22]  
GERMAIN DP, 2018, INTERNET, V375, P545, DOI DOI 10.1056/NEJMOA1510198
[23]   Neurodegeneration in the Niemann-Pick C mouse: Glial involvement [J].
German, DC ;
Liang, CL ;
Song, T ;
Yazdani, U ;
Xie, C ;
Dietschy, JM .
NEUROSCIENCE, 2002, 109 (03) :437-450
[24]   A novel, highly sensitive and specific biomarker for Niemann-Pick type C1 disease [J].
Giese, Anne-Katrin ;
Mascher, Hermann ;
Grittner, Ulrike ;
Eichler, Sabrina ;
Kramp, Guido ;
Lukas, Jan ;
Vruchte, Danielle Te ;
Al Eisa, Nada ;
Cortina-Borja, Mario ;
Porter, Forbes D. ;
Platt, Frances M. ;
Rolfs, Arndt .
ORPHANET JOURNAL OF RARE DISEASES, 2015, 10
[25]   New murine Niemann-Pick type C models bearing a pseudoexongenerating mutation recapitulate the main neurobehavioural and molecular features of the disease [J].
Gomez-Grau, Marta ;
Albaiges, Julia ;
Casas, Josefina ;
Auladell, Carme ;
Dierssen, Mara ;
Vilageliu, Lluisa ;
Grinberg, Daniel .
SCIENTIFIC REPORTS, 2017, 7
[26]  
HUANG X, 2018, INTERNET, V134, P3733, DOI DOI 10.1242/DEV.004572
[27]  
HUANG X, 2018, INTERNET, V132, P5115, DOI DOI 10.1242/DEV.02079
[28]  
HUGHES DA, 2018, INTERNET, V54, P288, DOI DOI 10.1136/JMEDGENET-2016-104178
[29]  
HUGHES MP, 2018, HUM MOL GENET, DOI DOI 10.1002/MAS.21349
[30]  
KIRKEGAARD T, 2014, INTERNET, V463, P549, DOI DOI 10.1038/NATURE08710