2008
DOI: 10.1186/1471-2407-8-237
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Similar reductions in the risk of human colon cancer by selective and nonselective cyclooxygenase-2 (COX-2) inhibitors

Abstract: Background: Epidemiologic and laboratory investigations suggest that aspirin and other nonsteroidal anti-inflammatory drugs (NSAIDs) have chemopreventive effects against colon cancer perhaps due at least in part to their activity against cyclooxygenase-2 (COX-2), the rate-limiting enzyme of the prostaglandin cascade.

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Cited by 67 publications
(45 citation statements)
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“…The use of NSAIDs decreases the number and size of colonic polyps in patients with familial adenomatous polyposis; similarly, aspirin has also been found to confer a protective effect on the colorectum in patients with Lynch syndrome (26,27). Over the past two decades, increasing evidence from epidemiological studies has identified a potential role in the prophylaxis of sporadic CRC, with an approximate 30% risk reduction with aspirin and non-aspirin NSAIDS and a potentially greater reduction with COXIB use (28,29). In general, a duration-dependent increase in risk reduction has been observed, with the greatest benefit seen after at least 10 years of continuous use.…”
Section: Aspirin Nsaids and Cox-2 Inhibitorsmentioning
confidence: 99%
“…The use of NSAIDs decreases the number and size of colonic polyps in patients with familial adenomatous polyposis; similarly, aspirin has also been found to confer a protective effect on the colorectum in patients with Lynch syndrome (26,27). Over the past two decades, increasing evidence from epidemiological studies has identified a potential role in the prophylaxis of sporadic CRC, with an approximate 30% risk reduction with aspirin and non-aspirin NSAIDS and a potentially greater reduction with COXIB use (28,29). In general, a duration-dependent increase in risk reduction has been observed, with the greatest benefit seen after at least 10 years of continuous use.…”
Section: Aspirin Nsaids and Cox-2 Inhibitorsmentioning
confidence: 99%
“…[9] Evidence that COX-2 inhibition can prevent these types of cancer has been reported in the literature. [10][11][12][13] In a recent study, a dimethylamino pyrazolopyrimidine derivative (DPP) was identified as a potent inhibitor of PGE 2 production. [14] A further study confirmed the effect of DPP derivatives in vivo using a 24 h zymosan-injected mouse air pouch model.…”
mentioning
confidence: 99%
“…Comparative studies of breast cancer and other neoplasms During the time period 1987-2008, we conducted a series of epidemiologic studies of NSAIDs and cancers of the breast, prostate, colon and lung [57,59,61,69,79,[95][96][97][98][99] . Five of these studies focused on cancer of the breast.…”
Section: Human Studies Of Non-selective Cox-2 Inhibitors and Breast Cmentioning
confidence: 99%
“…There was no effect of acetaminophen, an analgesic without COX-2 inhibiting properties (OR = 1.02). The inverse pattern of risk for acetaminophen, low dose aspirin, regular aspirin, ibuprofen and coxibs was significant by a linear trend test (P < 0.05) suggesting that chemopreventive effects become progressively stronger with greater selective COX-2 inhibition.Comparative studies of breast cancer and other neoplasms During the time period 1987-2008, we conducted a series of epidemiologic studies of NSAIDs and cancers of the breast, prostate, colon and lung [57,59,61,69,79,[95][96][97][98][99] . Five of these studies focused on cancer of the breast.…”
mentioning
confidence: 99%