» Articles » PMID: 32695150

The PPAR Pocket: Renewed Opportunities for Drug Development

Overview
Journal PPAR Res
Publisher Wiley
Date 2020 Jul 23
PMID 32695150
Citations 7
Authors
Affiliations
Soon will be listed here.
Abstract

The past decade of PPAR research has dramatically improved our understanding of the structural and mechanistic bases for the diverging physiological effects of different classes of PPAR ligands. The discoveries that lie at the heart of these developments have enabled the design of a new class of PPAR ligands, capable of isolating central therapeutic effects of PPAR modulation, while displaying markedly lower toxicities than previous generations of PPAR ligands. This review examines the emerging framework around the design of these ligands and seeks to unite its principles with the development of new classes of ligands for PPAR and PPAR. The focus is on the relationships between the binding modes of ligands, their influence on PPAR posttranslational modifications, and gene expression patterns. Specifically, we encourage the design and study of ligands that primarily bind to the pockets of PPAR and PPAR. In support of this development, we highlight already reported ligands that if studied in the context of this new framework may further our understanding of the gene programs regulated by PPAR and PPAR. Moreover, recently developed pharmacological tools that can be utilized in the search for ligands with new binding modes are also presented.

Citing Articles

The Peroxisome Proliferator-Activated Receptors of Ray-Finned Fish: Unique Structures, Elusive Functions.

Boukouvala E, Krey G Biomolecules. 2024; 14(6).

PMID: 38927038 PMC: 11201486. DOI: 10.3390/biom14060634.


Naringenin and β-carotene convert human white adipocytes to a beige phenotype and elevate hormone- stimulated lipolysis.

Coulter A, Greenway F, Zhang D, Ghosh S, Coulter C, James S Front Endocrinol (Lausanne). 2023; 14():1148954.

PMID: 37143734 PMC: 10153092. DOI: 10.3389/fendo.2023.1148954.


New High-Throughput Screen Discovers Novel Ligands of Full-Length Nuclear Receptor LRH-1.

Malabanan M, Chapagain P, Haratipour Z, Choi W, Orun A, Blind R ACS Chem Biol. 2023; 18(5):1101-1114.

PMID: 37074920 PMC: 10404069. DOI: 10.1021/acschembio.2c00805.


Anti-Obesity and Anti-Inflammatory Effects of Novel Carvacrol Derivatives on 3T3-L1 and WJ-MSCs Cells.

Cacciatore I, Spalletta S, Di Rienzo A, Flati V, Fornasari E, Pierdomenico L Pharmaceuticals (Basel). 2023; 16(3).

PMID: 36986440 PMC: 10055808. DOI: 10.3390/ph16030340.


PPAR agonists attenuate lenalidomide's anti-myeloma activity in vitro and in vivo.

Sha Y, Wu J, Paul B, Zhao Y, Mathews P, Li Z Cancer Lett. 2022; 545:215832.

PMID: 35872263 PMC: 10355274. DOI: 10.1016/j.canlet.2022.215832.


References
1.
Bruning J, Chalmers M, Prasad S, Busby S, Kamenecka T, He Y . Partial agonists activate PPARgamma using a helix 12 independent mechanism. Structure. 2007; 15(10):1258-71. DOI: 10.1016/j.str.2007.07.014. View

2.
Chandra V, Huang P, Hamuro Y, Raghuram S, Wang Y, Burris T . Structure of the intact PPAR-gamma-RXR- nuclear receptor complex on DNA. Nature. 2008; 456(7220):350-6. PMC: 2743566. DOI: 10.1038/nature07413. View

3.
Motani A, Wang Z, Weiszmann J, McGee L, Lee G, Liu Q . INT131: a selective modulator of PPAR gamma. J Mol Biol. 2009; 386(5):1301-11. DOI: 10.1016/j.jmb.2009.01.025. View

4.
Higgins L, Mantzoros C . The Development of INT131 as a Selective PPARgamma Modulator: Approach to a Safer Insulin Sensitizer. PPAR Res. 2008; 2008:936906. PMC: 2522386. DOI: 10.1155/2008/936906. View

5.
Liberato M, Nascimento A, Ayers S, Lin J, Cvoro A, Silveira R . Medium chain fatty acids are selective peroxisome proliferator activated receptor (PPAR) γ activators and pan-PPAR partial agonists. PLoS One. 2012; 7(5):e36297. PMC: 3359336. DOI: 10.1371/journal.pone.0036297. View