An integrated omics analysis of eicosanoid biology

被引:404
作者
Buczynski, Matthew W.
Dumlao, Darren S.
Dennis, Edward A. [1 ]
机构
[1] Univ Calif San Diego, Dept Pharmacol, Dept Chem & Biochem, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
genomics; proteomics; lipidomics; cyclooxygenase; lipoxygenase; cytochrome P450; prostaglandin; leukotriene; eicosanoid; ACTIVATED-RECEPTOR-ALPHA; PROSTAGLANDIN-E SYNTHASE; GAMMA-GLUTAMYL-TRANSPEPTIDASE; PLATELET-TYPE; 12-LIPOXYGENASE; SOLUBLE EPOXIDE HYDROLASE; LEUKOTRIENE C-4 SYNTHASE; AMINO-ACID-SEQUENCE; HUMAN UDP-GLUCURONOSYLTRANSFERASES; HUMAN POLYMORPHONUCLEAR LEUKOCYTES; CYTOSOLIC PHOSPHOLIPASE A(2);
D O I
10.1194/jlr.R900004-JLR200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Eicosanoids have been implicated in a vast number of devastating inflammatory conditions, including arthritis, atherosclerosis, pain, and cancer. Currently, over a hundred different eicosanoids have been identified, with many having potent bioactive signaling capacity. These lipid metabolites are synthesized de novo by at least 50 unique enzymes, many of which have been cloned and characterized. Due to the extensive characterization of eicosanoid biosynthetic pathways, this field provides a unique framework for integrating genomics, proteomics, and metabolomics toward the investigation of disease pathology. To facilitate a concerted systems biology approach, this review outlines the proteins implicated in eicosanoid biosynthesis and signaling in human, mouse, and rat. Applications of the extensive genomic and lipidomic research to date illustrate the questions in eicosanoid signaling that could be uniquely addressed by a thorough analysis of the entire eicosanoid proteome.-Buczynski, M. W., D. S. Dumlao, and E. A. Dennis. An integrated omics analysis of eicosanoid biology. J. Lipid Res. 2009. 50: 1015-1038.
引用
收藏
页码:1015 / 1038
页数:24
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