You are here

Nat Rev Drug Discov DOI:10.1038/nrd4051

Validating therapeutic targets through human genetics.

Publication TypeJournal Article
Year of Publication2013
AuthorsPlenge, RM, Scolnick, EM, Altshuler, D
JournalNat Rev Drug Discov
Volume12
Issue8
Pages581-94
Date Published2013 Aug
ISSN1474-1784
KeywordsBiomarkers, Clinical Trials as Topic, Drug Discovery, Drugs, Investigational, Early Termination of Clinical Trials, Genetics, Medical, Humans, Models, Biological, Molecular Targeted Therapy, Pharmacogenetics, Treatment Failure
Abstract

More than 90% of the compounds that enter clinical trials fail to demonstrate sufficient safety and efficacy to gain regulatory approval. Most of this failure is due to the limited predictive value of preclinical models of disease, and our continued ignorance regarding the consequences of perturbing specific targets over long periods of time in humans. 'Experiments of nature' - naturally occurring mutations in humans that affect the activity of a particular protein target or targets - can be used to estimate the probable efficacy and toxicity of a drug targeting such proteins, as well as to establish causal rather than reactive relationships between targets and outcomes. Here, we describe the concept of dose-response curves derived from experiments of nature, with an emphasis on human genetics as a valuable tool to prioritize molecular targets in drug development. We discuss empirical examples of drug-gene pairs that support the role of human genetics in testing therapeutic hypotheses at the stage of target validation, provide objective criteria to prioritize genetic findings for future drug discovery efforts and highlight the limitations of a target validation approach that is anchored in human genetics.

URLhttp://dx.doi.org/10.1038/nrd4051
DOI10.1038/nrd4051
Pubmed

http://www.ncbi.nlm.nih.gov/pubmed/23868113?dopt=Abstract

Alternate JournalNat Rev Drug Discov
PubMed ID23868113