Scientific Publications

Disease allele-dependent small-molecule sensitivities in blood cells from monogenic diabetes.

Publication TypeJournal Article
AuthorsShaw, SY, Blodgett DM, Ma MS, Westly EC, Clemons PA, Subramanian A., and Schreiber SL
AbstractEven as genetic studies identify alleles that influence human disease susceptibility, it remains challenging to understand their functional significance and how they contribute to disease phenotypes. Here, we describe an approach to translate discoveries from human genetics into functional and therapeutic hypotheses by relating human genetic variation to small-molecule sensitivities. We use small-molecule probes modulating a breadth of targets and processes to reveal disease allele-dependent sensitivities, using cells from multiple individuals with an extreme form of diabetes (maturity onset diabetes of the young type 1, caused by mutation in the orphan nuclear receptor HNF4α). This approach enabled the discovery of small molecules that show mechanistically revealing and therapeutically relevant interactions with HNF4α in both lymphoblasts and pancreatic β-cells, including compounds that physically interact with HNF4α. Compounds including US Food and Drug Administration-approved drugs were identified that favorably modulate a critical disease phenotype, insulin secretion from β-cells. This method may suggest therapeutic hypotheses for other nonblood disorders.
Year of Publication2011
JournalProceedings of the National Academy of Sciences of the United States of America
Volume108
Issue2
Pages492-7
Date Published (YYYY/MM/DD)2011/01/11
ISSN Number0027-8424
DOI10.1073/pnas.1016789108
PubMedhttp://www.ncbi.nlm.nih.gov/pubmed/21183721?dopt=Abstract