PTGS2

Gene Information
 
Gene Symbol
PTGS2
 
Aliases
COX-2, COX2, GRIPGHS, PGG/HS, PGHS-2, PHS-2, hCox-2
 
Entrez Gene ID
 
Gene Name
Prostaglandin-endoperoxide synthase 2
 
Chromosomal Location
1q31.1
 
HGNC ID
 
Summary
Prostaglandin-endoperoxide synthase (PTGS), also known as cyclooxygenase, is the key enzyme in prostaglandin biosynthesis, and acts both as a dioxygenase and as a peroxidase. There are two isozymes of PTGS: a constitutive PTGS1 and an inducible PTGS2, which differ in their regulation of expression and tissue distribution. This gene encodes the inducible isozyme. It is regulated by specific stimulatory events, suggesting that it is responsible for the prostanoid biosynthesis involved in inflammation and mitogenesis. [provided by RefSeq, Feb 2009]
 
RefSeq DNA
 
RefSeq mRNA
  e!Ensembl
Gene
Transcript  
Protein

Gene Ontology (GO)

GO ID Ontology Function Evidence Reference
GO:0001516 Biological process Prostaglandin biosynthetic process NAS 20448152
GO:0010575 Biological process Positive regulation of vascular endothelial growth factor production ISS 9630216
GO:0019371 Biological process Cyclooxygenase pathway IDA 1380156
GO:0031394 Biological process Positive regulation of prostaglandin biosynthetic process NAS 20448152
GO:0045429 Biological process Positive regulation of nitric oxide biosynthetic process ISS 9630216
Protein Information
 
Protein Name
Prostaglandin G/H synthase 2, PGH synthase 2, PHS II, cyclooxygenase 2, cyclooxygenase 2b, prostaglandin H2 synthase 2, prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase)
 
Function
Converts arachidonate to prostaglandin H2 (PGH2), a committed step in prostanoid synthesis (PubMed:26859324, PubMed:27226593). Constitutively expressed in some tissues in physiological conditions, such as the endothelium, kidney and brain, and in pathological conditions, such as in cancer. PTGS2 is responsible for production of inflammatory prostaglandins. Up-regulation of PTGS2 is also associated with increased cell adhesion, phenotypic changes, resistance to apoptosis and tumor angiogenesis. In cancer cells, PTGS2 is a key step in the production of prostaglandin E2 (PGE2), which plays important roles in modulating motility, proliferation and resistance to apoptosis. During neuroinflammation, plays a role in neuronal secretion of specialized preresolving mediators (SPMs), especially 15-R-lipoxin A4, that regulates phagocytic microglia (By similarity).
 
Refseq Proteins
 
UniProt
 
PDB
 
Pfam
Pfam Accession Pfam ID
PF03098 An_peroxidase
PF00008 EGF
Pathways
 
KEGG
 
Reactome
 

Arachidonic acid metabolism
Metabolic pathways
NF-kappa B signaling pathway
VEGF signaling pathway
C-type lectin receptor signaling pathway
IL-17 signaling pathway
TNF signaling pathway
Retrograde endocannabinoid signaling
Serotonergic synapse
Ovarian steroidogenesis
Oxytocin signaling pathway
Regulation of lipolysis in adipocytes
Leishmaniasis
Human cytomegalovirus infection
Human papillomavirus infection
Kaposi sarcoma-associated herpesvirus infection
Pathways in cancer
Chemical carcinogenesis
MicroRNAs in cancer
Small cell lung cancer

 

Nicotinamide salvaging
Synthesis of 15-eicosatetraenoic acid derivatives
Synthesis of Prostaglandins (PG) and Thromboxanes (TX)
Interleukin-10 signaling
Interleukin-4 and Interleukin-13 signaling
Biosynthesis of DHA-derived SPMs
Biosynthesis of EPA-derived SPMs
Biosynthesis of DPAn-3 SPMs
Biosynthesis of electrophilic ω-3 PUFA oxo-derivatives

Interactions
 
STRING MINT IntAct
ENSP00000218388 P01033 P01033
    View interactions
     

Associated Diseases

Disease groupDisease NameReferences
Cardiovascular Diseases
Heart Failure
Aortic Aneurysm
Cardiomyopathy
Chylopericardium
Arteriosclerosis
References
 

Inflammation and Human Ovarian Follicular Dynamics.

Boots Christina E, Jungheim Emily S
Department of Obstetrics and Gynecology, Washington University, St. Louis, Missouri.| Department of Obstetrics and Gynecology, Washington University, St. Louis, Missouri.
Semin Reprod Med. 2015 Jul;33(4):270-5. doi: 10.1055/s-0035-1554928. Epub 2015

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