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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.1002/cpt.639</dc:identifier><dc:language>eng</dc:language><dc:creator>Patrignani, P</dc:creator><dc:creator>Sacco, A</dc:creator><dc:creator>Sostres, C</dc:creator><dc:creator>Bruno, A</dc:creator><dc:creator>Dovizio, M</dc:creator><dc:creator>Piazuelo, E</dc:creator><dc:creator>Di Francesco, L</dc:creator><dc:creator>Contursi, A</dc:creator><dc:creator>Zucchelli, M</dc:creator><dc:creator>Schiavone, S</dc:creator><dc:creator>Tacconelli, S</dc:creator><dc:creator>Patrono, C</dc:creator><dc:creator>Lanas, A.</dc:creator><dc:title>Low-dose aspirin acetylates cyclooxygenase-1 in human colorectal mucosa: implications for the chemoprevention of colorectal cancer.</dc:title><dc:identifier>ART-2017-97965</dc:identifier><dc:description>The mechanism of action of low-dose aspirin in the prevention of colorectal cancer (CRC) remains largely hypothetical. We aimed to compare the effects of low-dose aspirin (100 mg/day for 7 days) given to 40 individuals undergoing CRC screening on the extent of cyclooxygenase (COX)-1 acetylation at serine-529 (AceCOX-1), in blood platelets vs colorectal mucosa, at 7 (group 1) and 24 hours (group 2) after dosing. A significantly (P&lt;0.01) lower %AceCOX-1 was detected in colonic and rectal mucosa (average 64%) vs platelets (average 75%) in both groups. This effect was associated with an average 46% (P&lt;0.01) and 35% (P&lt;0.05) reduction in prostaglandin (PG) E2 levels and phosphorylated S6 (p-S6) levels, respectively. Rectal mucosal levels of p-S6/S6 significantly(P&lt;0.01) correlated with PGE2. These findings demonstrate that low-dose aspirin produces long-lasting acetylation of COX-1 and down-regulation of p-S6 in human colorectal mucosa, an effect that may interfere with early colorectal carcinogenesis.</dc:description><dc:date>2017</dc:date><dc:source>http://zaguan.unizar.es/record/64496</dc:source><dc:doi>10.1002/cpt.639</dc:doi><dc:identifier>http://zaguan.unizar.es/record/64496</dc:identifier><dc:identifier>oai:zaguan.unizar.es:64496</dc:identifier><dc:identifier.citation>CLINICAL PHARMACOLOGY &amp; THERAPEUTICS 36 (2017), [29 pp.]</dc:identifier.citation><dc:rights>All rights reserved</dc:rights><dc:rights>http://www.europeana.eu/rights/rr-f/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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