4.5 Review

Simple animal models for amyotrophic lateral sclerosis drug discovery

Journal

EXPERT OPINION ON DRUG DISCOVERY
Volume 11, Issue 8, Pages 797-804

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/17460441.2016.1196183

Keywords

Amyotrophic lateral sclerosis; C; elegans; chemical genetics; Drosophila; drug discovery; zebrafish

Funding

  1. Frick Foundation for ALS Research
  2. Genome Quebec/Canada
  3. ALSA (USA)
  4. Brain Canada Foundation
  5. US Dept. of Defence/CDMRP/ALSRP
  6. Weston Brain Institute
  7. CQDM & Ontario Centres of Excellence
  8. Canada Foundation for Innovation
  9. CIHR
  10. Natural Sciences and Engineering Research Council of Canada

Ask authors/readers for more resources

Introduction: Simple animal models have enabled great progress in uncovering the disease mechanisms of amyotrophic lateral sclerosis (ALS) and are helping in the selection of therapeutic compounds through chemical genetic approaches.Areas covered: Within this article, the authors provide a concise overview of simple model organisms, C. elegans, Drosophila and zebrafish, which have been employed to study ALS and discuss their value to ALS drug discovery. In particular, the authors focus on innovative chemical screens that have established simple organisms as important models for ALS drug discovery.Expert opinion: There are several advantages of using simple animal model organisms to accelerate drug discovery for ALS. It is the authors' particular belief that the amenability of simple animal models to various genetic manipulations, the availability of a wide range of transgenic strains for labelling motoneurons and other cell types, combined with live imaging and chemical screens should allow for new detailed studies elucidating early pathological processes in ALS and subsequent drug and target discovery.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available