Systems Pharmacology Links GPCRs with Retinal Degenerative Disorders

被引:27
作者
Chen, Yu [1 ,2 ]
Palczewski, Krzysztof [3 ]
机构
[1] Shanghai Univ Tradit Chinese Med, Yueyang Hosp, Shanghai 200437, Peoples R China
[2] Shanghai Univ Tradit Chinese Med, Clin Res Inst Integrat Med, Shanghai 200437, Peoples R China
[3] Case Western Reserve Univ, Sch Med, Dept Pharmacol, Cleveland, OH 44106 USA
来源
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, VOL 56 | 2016年 / 56卷
关键词
network; systems biology; pharmacological agents; polypharmacology; retina; blindness; PROTEIN-COUPLED RECEPTORS; DRUG DISCOVERY; SUPEROXIDE-PRODUCTION; STARGARDT DISEASE; DRUGGABLE GENOME; NADPH OXIDASES; BIOLOGY; POLYPHARMACOLOGY; NETWORK; MECHANISMS;
D O I
10.1146/annurev-pharmtox-010715-103033
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In most biological systems, second messengers and their key regulatory and effector proteins form links between multiple cellular signaling pathways. Such signaling nodes can integrate the deleterious effects of genetic aberrations, environmental stressors, or both in complex diseases, leading to cell death by various mechanisms. Here we present a systems (network) pharmacology approach that, together with transcriptomics analyses, was used to identify different G protein-coupled receptors that experimentally protected against cellular stress and death caused by linked signaling mechanisms. We describe the application of this concept to degenerative and diabetic retinopathies in appropriate mouse models as an example. Systems pharmacology also provides an attractive framework for devising strategies to combat complex diseases by using (repurposing) US Food and Drug Administration-approved pharmacological agents.
引用
收藏
页码:273 / 298
页数:26
相关论文
共 98 条
[1]   Proof of Concept: Network and Systems Biology Approaches Aid in the Discovery of Potent Anticancer Drug Combinations [J].
Azmi, Asfar S. ;
Wang, Zhiwei ;
Philip, Philip A. ;
Mohammad, Ramzi M. ;
Sarkar, Fazlul H. .
MOLECULAR CANCER THERAPEUTICS, 2010, 9 (12) :3137-3144
[2]  
Barbaric Ivana, 2007, Briefings in Functional Genomics & Proteomics, V6, P91, DOI 10.1093/bfgp/elm008
[3]   The NOX family of ROS-generating NADPH oxidases: Physiology and pathophysiology [J].
Bedard, Karen ;
Krause, Karl-Heinz .
PHYSIOLOGICAL REVIEWS, 2007, 87 (01) :245-313
[4]   Network analyses in systems pharmacology [J].
Berger, Seth I. ;
Iyengar, Ravi .
BIOINFORMATICS, 2009, 25 (19) :2466-2472
[5]   Automated design of ligands to polypharmacological profiles [J].
Besnard, Jeremy ;
Ruda, Gian Filippo ;
Setola, Vincent ;
Abecassis, Keren ;
Rodriguiz, Ramona M. ;
Huang, Xi-Ping ;
Norval, Suzanne ;
Sassano, Maria F. ;
Shin, Antony I. ;
Webster, Lauren A. ;
Simeons, Frederick R. C. ;
Stojanovski, Laste ;
Prat, Annik ;
Seidah, Nabil G. ;
Constam, Daniel B. ;
Bickerton, G. Richard ;
Read, Kevin D. ;
Wetsel, William C. ;
Gilbert, Ian H. ;
Roth, Bryan L. ;
Hopkins, Andrew L. .
NATURE, 2012, 492 (7428) :215-+
[6]   The agony and ecstasy of "OMIC" technologies in drug development [J].
Bilello, JA .
CURRENT MOLECULAR MEDICINE, 2005, 5 (01) :39-52
[7]   Extension of life-span by introduction of telomerase into normal human cells [J].
Bodnar, AG ;
Ouellette, M ;
Frolkis, M ;
Holt, SE ;
Chiu, CP ;
Morin, GB ;
Harley, CB ;
Shay, JW ;
Lichtsteiner, S ;
Wright, WE .
SCIENCE, 1998, 279 (5349) :349-352
[8]  
Boran ADW, 2010, CURR OPIN DRUG DISC, V13, P297
[9]   Regulation of superoxide production in neutrophils: role of calcium influx [J].
Brechard, Sabrina ;
Tschirhart, Eric J. .
JOURNAL OF LEUKOCYTE BIOLOGY, 2008, 84 (05) :1223-1237
[10]   Systems Biology and Systems Chemistry: New Directions for Drug Discovery [J].
Brown, J. B. ;
Okuno, Yasushi .
CHEMISTRY & BIOLOGY, 2012, 19 (01) :23-28