» Articles » PMID: 24512192

NOX2 As a Target for Drug Development: Indications, Possible Complications, and Progress

Overview
Specialty Endocrinology
Date 2014 Feb 12
PMID 24512192
Citations 35
Authors
Affiliations
Soon will be listed here.
Abstract

Significance: NOX2 is important for host defense, and yet is implicated in a large number of diseases in which inflammation plays a role in pathogenesis. These include acute and chronic lung inflammatory diseases, stroke, traumatic brain injury, and neurodegenerative diseases, including Alzheimer's and Parkinson's Diseases.

Recent Advances: Recent drug development programs have targeted several NOX isoforms that are implicated in a variety of diseases. The focus has been primarily on NOX4 and NOX1 rather than on NOX2, due, in part, to concerns about possible immunosuppressive side effects. Nevertheless, NOX2 clearly contributes to the pathogenesis of many inflammatory diseases, and its inhibition is predicted to provide a novel therapeutic approach.

Critical Issues: Possible side effects that might arise from targeting NOX2 are discussed, including the possibility that such inhibition will contribute to increased infections and/or autoimmune disorders. The state of the field with regard to existing NOX2 inhibitors and targeted development of novel inhibitors is also summarized.

Future Directions: NOX2 inhibitors show particular promise for the treatment of inflammatory diseases, both acute and chronic. Theoretical side effects include pro-inflammatory and autoimmune complications and should be considered in any therapeutic program, but in our opinion, available data do not indicate that they are sufficiently likely to eliminate NOX2 as a drug target, particularly when weighed against the seriousness of many NOX2-related indications. Model studies demonstrating efficacy with minimal side effects are needed to encourage future development of NOX2 inhibitors as therapeutic agents.

Citing Articles

Quercetin Mitigates Lysophosphatidylcholine (LPC)-Induced Neutrophil Extracellular Traps (NETs) Formation through Inhibiting the P2X7R/P38MAPK/NOX2 Pathway.

Liu S, Wang Y, Ying L, Li H, Zhang K, Liang N Int J Mol Sci. 2024; 25(17).

PMID: 39273358 PMC: 11395007. DOI: 10.3390/ijms25179411.


Ribociclib leverages phosphodiesterase 4 inhibition in the treatment of neutrophilic inflammation and acute respiratory distress syndrome.

Chen P, Chen S, Chen Y, Wang Y, Lin C, Chen C J Adv Res. 2024; 62:229-243.

PMID: 38548264 PMC: 11331181. DOI: 10.1016/j.jare.2024.03.019.


Structure of human phagocyte NADPH oxidase in the activated state.

Liu X, Shi Y, Liu R, Song K, Chen L Nature. 2024; 627(8002):189-195.

PMID: 38355798 DOI: 10.1038/s41586-024-07056-1.


Cardiac endothelial ischemia/reperfusion injury-derived protein damage-associated molecular patterns disrupt the integrity of the endothelial barrier.

Kumphune S, Seenak P, Paiyabhrom N, Songjang W, Pankhong P, Jumroon N Heliyon. 2024; 10(2):e24600.

PMID: 38312663 PMC: 10835233. DOI: 10.1016/j.heliyon.2024.e24600.


Novel NADPH Oxidase-2 Inhibitors as Potential Anti-Inflammatory and Neuroprotective Agents.

Juric M, Rawat V, Amaradhi R, Zielonka J, Ganesh T Antioxidants (Basel). 2023; 12(9).

PMID: 37759963 PMC: 10525516. DOI: 10.3390/antiox12091660.


References
1.
Csanyi G, Cifuentes-Pagano E, Al Ghouleh I, Ranayhossaini D, Egana L, Lopes L . Nox2 B-loop peptide, Nox2ds, specifically inhibits the NADPH oxidase Nox2. Free Radic Biol Med. 2011; 51(6):1116-25. PMC: 3204933. DOI: 10.1016/j.freeradbiomed.2011.04.025. View

2.
Harper R, Xu C, Eiserich J, Chen Y, Kao C, Thai P . Differential regulation of dual NADPH oxidases/peroxidases, Duox1 and Duox2, by Th1 and Th2 cytokines in respiratory tract epithelium. FEBS Lett. 2005; 579(21):4911-7. DOI: 10.1016/j.febslet.2005.08.002. View

3.
Feng Y, Forgac M . Inhibition of vacuolar H(+)-ATPase by disulfide bond formation between cysteine 254 and cysteine 532 in subunit A. J Biol Chem. 1994; 269(18):13224-30. View

4.
Sanchez G, Pedrozo Z, Domenech R, Hidalgo C, Donoso P . Tachycardia increases NADPH oxidase activity and RyR2 S-glutathionylation in ventricular muscle. J Mol Cell Cardiol. 2005; 39(6):982-91. DOI: 10.1016/j.yjmcc.2005.08.010. View

5.
Stefanska J, Sarniak A, Wlodarczyk A, Sokolowska M, Doniec Z, Bialasiewicz P . Hydrogen peroxide and nitrite reduction in exhaled breath condensate of COPD patients. Pulm Pharmacol Ther. 2012; 25(5):343-8. DOI: 10.1016/j.pupt.2012.06.001. View