Trends in GPCR drug discovery: new agents, targets and indications

被引:1841
作者
Hauser, Alexander S. [1 ]
Attwood, Misty M. [2 ]
Rask-Andersen, Mathias [3 ]
Schioth, Helgi B. [2 ]
Gloriam, David E. [1 ]
机构
[1] Univ Copenhagen, Fac Hlth & Med Sci, Dept Drug Design & Pharmacol, DK-2100 Copenhagen, Denmark
[2] Uppsala Univ, Dept Neurosci Funct Pharmacol, S-75105 Uppsala, Sweden
[3] Uppsala Univ, Sci Life Lab, Dept Immunol Genet & Pathol, S-75105 Uppsala, Sweden
基金
欧洲研究理事会;
关键词
PROTEIN-COUPLED RECEPTORS; FORMYL PEPTIDE RECEPTORS; INTERNATIONAL UNION; THERAPEUTIC TARGETS; BIASED AGONISM; PHARMACOLOGY; LIGANDS; OPPORTUNITIES; PLACEBO; PHASE-2;
D O I
10.1038/nrd.2017.178
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
G protein-coupled receptors (GPCRs) are the most intensively studied drug targets, mostly due to their substantial involvement in human pathophysiology and their pharmacological tractability. Here, we report an up-to-date analysis of all GPCR drugs and agents in clinical trials, which reveals current trends across molecule types, drug targets and therapeutic indications, including showing that 475 drugs (similar to 34% of all drugs approved by the US Food and Drug Administration (FDA)) act at 108 unique GPCRs. Approximately 321 agents are currently in clinical trials, of which similar to 20% target 66 potentially novel GPCR targets without an approved drug, and the number of biological drugs, allosteric modulators and biased agonists has increased. The major disease indications for GPCR modulators show a shift towards diabetes, obesity and Alzheimer disease, although several central nervous system disorders are also highly represented. The 224 (56%) non-olfactory GPCRs that have not yet been explored in clinical trials have broad untapped therapeutic potential, particularly in genetic and immune system disorders. Finally, we provide an interactive online resource to analyse and infer trends in GPCR drug discovery.
引用
收藏
页码:829 / 842
页数:14
相关论文
共 100 条
[1]   Alignment-free d2* oligonucleotide frequency dissimilarity measure improves prediction of hosts from metagenomically-derived viral sequences [J].
Ahlgren, Nathan A. ;
Ren, Jie ;
Lu, Yang Young ;
Fuhrman, Jed A. ;
Sun, Fengzhu .
NUCLEIC ACIDS RESEARCH, 2017, 45 (01) :39-53
[2]   Allosteric "beta-blocker" isolated from a DNA-encoded small molecule library [J].
Ahn, Seungkirl ;
Kahsai, Alem W. ;
Pani, Biswaranjan ;
Wang, Qin-Ting ;
Zhao, Shuai ;
Wall, Alissa L. ;
Strachan, Ryan T. ;
Staus, Dean P. ;
Wingler, Laura M. ;
Sun, Lillian D. ;
Sinnaeve, Justine ;
Choi, Minjung ;
Cho, Ted ;
Xu, Thomas T. ;
Hansen, Gwenn M. ;
Burnett, Michael B. ;
Lamerdin, Jane E. ;
Bassoni, Daniel L. ;
Gavino, Bryant J. ;
Husemoen, Gitte ;
Olsen, Eva K. ;
Franch, Thomas ;
Costanzi, Stefano ;
Chen, Xin ;
Lefkowitz, Robert J. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2017, 114 (07) :1708-1713
[3]   Polypharmacology: Challenges and Opportunities in Drug Discovery [J].
Anighoro, Andrew ;
Bajorath, Juergen ;
Rastelli, Giulio .
JOURNAL OF MEDICINAL CHEMISTRY, 2014, 57 (19) :7874-7887
[4]  
[Anonymous], 2013, IDF DIABETES ATLAS
[5]   G Protein-Coupled Receptors in Cancer [J].
Bar-Shavit, Rachel ;
Maoz, Myriam ;
Kancharla, Arun ;
Nag, Jeetendra Kumar ;
Agranovich, Daniel ;
Grisaru-Granovsky, Sorina ;
Uziely, Beatrice .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2016, 17 (08)
[6]   In vivo veritas, the next frontier for functionally selective GPCR ligands [J].
Beaulieu, Jean Martin .
METHODS, 2016, 92 :64-71
[7]   Enhanced morphine analgesia in mice lacking β-arrestin 2 [J].
Bohn, LM ;
Lefkowitz, RJ ;
Gainetdinov, RR ;
Peppel, K ;
Caron, MG ;
Lin, FT .
SCIENCE, 1999, 286 (5449) :2495-2498
[8]   A Clinical Study of Lupron Depot in the Treatment of Women with Alzheimer's Disease: Preservation of Cognitive Function in Patients Taking an Acetylcholinesterase Inhibitor and Treated with High Dose Lupron Over 48 Weeks [J].
Bowen, Richard L. ;
Perry, George ;
Xiong, Chengjie ;
Smith, Mark A. ;
Atwood, Craig S. .
JOURNAL OF ALZHEIMERS DISEASE, 2015, 44 (02) :549-560
[9]   Fingolimod (FTY720): discovery and development of an oral drug to treat multiple sclerosis [J].
Brinkmann, Volker ;
Billich, Andreas ;
Baumruker, Thomas ;
Heining, Peter ;
Schmouder, Robert ;
Francis, Gordon ;
Aradhye, Shreeram ;
Burtin, Pascale .
NATURE REVIEWS DRUG DISCOVERY, 2010, 9 (11) :883-897
[10]   Recognition of Bacterial Signal Peptides by Mammalian Formyl Peptide Receptors A NEW MECHANISM FOR SENSING PATHOGENS [J].
Bufe, Bernd ;
Schumann, Timo ;
Kappl, Reinhard ;
Bogeski, Ivan ;
Kummerow, Carsten ;
Podgorska, Marta ;
Smola, Sigrun ;
Hoth, Markus ;
Zufall, Frank .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2015, 290 (12) :7369-7387