Title : Effect of eicosapentaenoic acid on E-type prostaglandin synthesis and EP4 receptor signaling in human colorectal cancer cells.

Pub. Date : 2010 Aug

PMID : 20689756






6 Functional Relationships(s)
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1 EPA-FFA in cell culture medium was incorporated rapidly into phospholipid membranes of HCA-7 human CRC cells and acted as a substrate for COX-2, leading to reduced synthesis of PGE(2) and generation of PGE(3). Prostaglandins E mitochondrially encoded cytochrome c oxidase II Homo sapiens
2 EPA-FFA in cell culture medium was incorporated rapidly into phospholipid membranes of HCA-7 human CRC cells and acted as a substrate for COX-2, leading to reduced synthesis of PGE(2) and generation of PGE(3). Prostaglandins E mitochondrially encoded cytochrome c oxidase II Homo sapiens
3 We conclude that EPA-FFA drives a COX-2-dependent "PGE(2)-to-PGE(3) switch" in human CRC cells and that PGE(3) acts as a partial agonist at the PGE(2) EP4 receptor. Prostaglandins E mitochondrially encoded cytochrome c oxidase II Homo sapiens
4 We conclude that EPA-FFA drives a COX-2-dependent "PGE(2)-to-PGE(3) switch" in human CRC cells and that PGE(3) acts as a partial agonist at the PGE(2) EP4 receptor. Prostaglandins E mitochondrially encoded cytochrome c oxidase II Homo sapiens
5 We conclude that EPA-FFA drives a COX-2-dependent "PGE(2)-to-PGE(3) switch" in human CRC cells and that PGE(3) acts as a partial agonist at the PGE(2) EP4 receptor. Prostaglandins E mitochondrially encoded cytochrome c oxidase II Homo sapiens
6 We conclude that EPA-FFA drives a COX-2-dependent "PGE(2)-to-PGE(3) switch" in human CRC cells and that PGE(3) acts as a partial agonist at the PGE(2) EP4 receptor. Prostaglandins E mitochondrially encoded cytochrome c oxidase II Homo sapiens