Abstract
There is epidemiological evidence that suggests an inverse association between the consumption of non-steroidal anti-inflammatories (NSAIDs) and the risk of developing certain neoplasms. This association led to the identification of the therapeutic target of these drugs, cyclooxygenase type 2 (COX-2). Later studies have demonstrated that COX-2 is over-expressed in many malignant and pre-malignant lesions of different origins, among which are included colorectal neoplasms. This factor explains the beneficial effect observed with the use of classic NSAIDs and more recently, with selective COX-2 inhibitors (coxibs), in the treatment and/or prevention of several neoplasms.
MeSH terms
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Adenocarcinoma / drug therapy
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Adenocarcinoma / enzymology*
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Adenocarcinoma / epidemiology
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Adenocarcinoma / genetics
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Adenocarcinoma / prevention & control
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Adenocarcinoma / surgery
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Adenoma / drug therapy
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Adenoma / enzymology
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Adenoma / prevention & control
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Adenomatous Polyposis Coli / drug therapy
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Adenomatous Polyposis Coli / enzymology
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Adenomatous Polyposis Coli / genetics
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Adenomatous Polyposis Coli / surgery
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Adult
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Clinical Trials as Topic
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Colorectal Neoplasms / drug therapy
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Colorectal Neoplasms / enzymology*
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Colorectal Neoplasms / epidemiology
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Colorectal Neoplasms / genetics
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Colorectal Neoplasms / prevention & control
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Colorectal Neoplasms / surgery
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Combined Modality Therapy
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Cyclooxygenase 2 / physiology*
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Cyclooxygenase 2 Inhibitors / pharmacology
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Cyclooxygenase 2 Inhibitors / therapeutic use*
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Humans
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Multicenter Studies as Topic
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Neoplasm Proteins / physiology*
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Precancerous Conditions / drug therapy
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Precancerous Conditions / enzymology
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Prognosis
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Risk
Substances
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Cyclooxygenase 2 Inhibitors
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Neoplasm Proteins
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Cyclooxygenase 2