posted on 2016-06-07, 00:00authored byNivanthika K. Wimalasena, Viet Q. Le, Kandatege Wimalasena, Stuart L. Schreiber, Rakesh Karmacharya
We carried out a
gene expression-based in silico screen in order to
identify small molecules with gene-expression profiles that are anticorrelated
with a gene-expression profile for Parkinson’s disease (PD).
We identified the cyclin-dependent kinase 2/5 (CDK2/5) inhibitor GW8510
as our most significant hit and characterized its effects in rodent
MN9D cells and in human neuronal cells derived from induced pluripotent
stem cells. GW8510 demonstrated neuroprotective ability in MN9D cells
in the presence of 1-methyl-4-phenylpyridium (MPP+), a
widely used neurotoxin model for Parkinson’s disease. In order
to delineate the nature and extent of GW8510’s neuroprotective
properties, we studied GW8510 in human neuronal cells in the context
of various mechanisms of cellular stress. We found that GW8510 was
protective against small-molecule mitochondrial and endoplasmic reticulum
stressors. Our findings illustrate an approach to using small-molecule
gene expression libraries to identify compounds with therapeutic potential
in human diseases.