Endometriosis is an inflammation-dependent gynecologic disorder. Increased cyclooxygenase-2 (COX-2) expression plays an important role in the development and progression of endometriosis. Lipoxin A (LXA) is an endogenous anti-inflammation lipid and showed inhibitory effects on the development of endometriosis; however， the mechanism remains unclear. In this study， the overexpression of COX-2 was observed in ectopic endometrium of endometriosis patients compared to the normal endometrium of controls. Lipoxin A efficiently suppressed IL-1β-induced COX-2 protein expression in ectopic endometriotic stromal cells (ESCs) via its receptor， formyl peptide receptor 2/lipoxin A receptor (FPR2/ALX). Antagonism of FPR2/ALX eliminated the inhibitory effect by LXA. IL-1β induced the activation of mitogen-activated protein kinases (MAPKs)， which can promote the expression of COX-2. Pretreatment of ESCs with LXA inhibited the phosphorylation of p38 MAPK induced by IL-1β. These findings suggest that inflammation and MAPKs pathways respond for the abnormal expression of COX-2， which can elucidate the pathophysiology of endometriosis. Moreover， LXA suppressed IL-1β-induced COX-2 expression through inhibiting the p38 MAPK signaling protein. This research contributes for better understanding of the cellular and biological events of inflammation and anti-inflammation-mediated regulation in endometriosis.