Affiliation:
1. University Department of Surgery, City Hospital, Dudley Road, Birmingham and Clinical Research Block, Queen Elizabeth Hospital, Birmingham, UK
Abstract
Abstract
Experimental, clinical and epidemiological studies have implicated arachidonic acid and its metabolites as important mediators in colorectal carcinogenesis. Although arachidonic acid levels are increased in tumour membrane lipids, its availability for metabolic processes is not known. The activities of phospholipase A2 (PLA2) and diacylglycerol lipase therefore were assessed in tumour and normal mucosal specimens from 20 patients with colorectal cancer using 14C-radiolabelled substrates. The median (interquartile range) PLA2 activity was increased in tumour tissue (10.5 (6.0, 18.5) pmol arachidonic acid mg−1 h−1) compared with that in normal mucosa (5.6 (2.5, 8.5) pmol arachidonic acid mg−1 h−1) (P < 0.001, Wilcoxon signed rank test). Activity of diacylglycerol lipase was also greater in tumoral tissue (47.4 (21.6, 82.1) pmol arachidonic acid mg−1 h−1) than in mucosa (19.1 (9.4, 42.9) pmol arachidonic acid mg−1 h−1) (P < 0.005). There was no correlation between either PLA2 or diacylglycerol lipase activity and myeloperoxidase activity, suggesting that these increases were not directly attributable to tumour inflammatory cell infiltrate. Augmentation of arachidonic acid release in colorectal tumours may have implications for therapy.
Publisher
Oxford University Press (OUP)
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