Target intelligence / Profile preview

Phospholipase A2 (PLA2) (PLA2)

Target
PLA2
Molecular classification
Enzyme, Hydrolase, Phospholipase
01

Overview

The arachidonic acid release machinery refers to the enzymatic system, predominantly centered on the Phospholipase A2 (PLA2) family, responsible for liberating arachidonic acid from the sn-2 position of membrane phospholipids (UniProt P47712). Cytosolic phospholipase A2 (cPLA2) is the primary isoform involved in this process during inflammatory signaling, activated by increases in intracellular calcium and phosphorylation by MAP kinases (PubMed PMID: 21532552). Once released, arachidonic acid acts as the rate-limiting precursor for the eicosanoid pathway, leading to the production of prostaglandins, leukotrienes, and thromboxanes (StatPearls, Arachidonic Acid Metabolism). This machinery is a critical focal point in the inflammatory response, making it a major target for anti-inflammatory therapy. Glucocorticoids are the most well-known class of drugs that modulate this system, primarily by inducing the expression of annexins (lipocortins) which inhibit PLA2 activity (PubMed PMID: 15914678). While direct inhibitors of PLA2 isoforms like varespladib and darapladib have been developed, achieving clinical success has been difficult due to the complex redundancy and physiological roles of different PLA2 enzymes in cellular homeostasis.

Other names
cPLA2Cytosolic phospholipase A2PLA2G4APhosphatidylcholine 2-acylhydrolaseArachidonyl-specific phospholipase A2sPLA2Secretory phospholipase A2
02

Mechanism of action

Inhibition of the enzymatic hydrolysis of membrane phospholipids at the sn-2 position, preventing the liberation of arachidonic acid and subsequent production of pro-inflammatory eicosanoids.

03

Biological functions

Lipid metabolismSignal transductionInflammationEicosanoid biosynthesisCell signaling
04

Disease associations

InflammationAsthmaRheumatoid arthritisCardiovascular diseaseCancerNeurodegenerative disease
05

Safety considerations

Gastrointestinal toxicityBroad immunosuppressionInterference with homeostatic lipid signalingPotential cardiovascular risk associated with specific isoform inhibition
06

Interacting drugs

Dexamethasone

5 more in the full profile.

07

Biomarkers

Arachidonic acid levelsProstaglandin E2 (PGE2)Leukotriene B4 (LTB4)C-reactive protein (CRP)

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