Overexpression of the enzyme COX-2 (cyclo-oxygenase-2) is associated with various pathophysiological conditions, including inflammatory diseases and different cancers. Increased synthesis of COX-2 in fetal membranes and the myometrium is also linked with the onset of term and preterm labour. COX-2 gene regulation is controlled at various levels including gene transcription and post-transcriptional events. The present article focuses on the complexity of COX-2 gene regulation and reviews current concepts that highlight: (i) transcription of COX-2 is induced rapidly and transiently in response to a plethora of stimuli; (ii) COX-2 mRNA stability and translational efficiency is governed by multiple regulatory elements within the 3′-untranslated region; (iii) specific microRNAs and RNA-binding proteins influence COX-2 mRNA stability; and (iv) regulation of COX-2 involves alternative polyadenylation.
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June 2008
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Conference Article|
May 21 2008
Complexity of COX-2 gene regulation
Kelly A. Harper;
Kelly A. Harper
1Institute of Cellular Medicine, The Medical School, Newcastle University, Newcastle upon Tyne NE2 4HH, U.K.
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Alison J. Tyson-Capper
Alison J. Tyson-Capper
1
1Institute of Cellular Medicine, The Medical School, Newcastle University, Newcastle upon Tyne NE2 4HH, U.K.
1To whom correspondence should be addressed (email A.J.Tyson-Capper@ncl.ac.uk).
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Biochem Soc Trans (2008) 36 (3): 543–545.
Article history
Received:
February 06 2008
Citation
Kelly A. Harper, Alison J. Tyson-Capper; Complexity of COX-2 gene regulation. Biochem Soc Trans 1 June 2008; 36 (3): 543–545. doi: https://doi.org/10.1042/BST0360543
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