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Cyclooxygenase 2: a molecular target for cancer prevention and treatment

机译:环氧合酶2:预防和治疗癌症的分子靶标

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摘要

Cyclooxygenase 2 (COX-2), an inducible prostaglandin G/H synthase, is overexpressed in several human cancers. Here, the potential utility of selective COX-2 inhibitors in the prevention and treatment of cancer is considered. The mechanisms by which COX-2 levels increase in cancers, key data that indicate a causal link between increased COX-2 activity and tumorigenesis, and possible mechanisms of action of COX-2 are discussed. In a proof-of-principle clinical trial, treatment with the selective COX-2 inhibitor celecoxib reduced the number of colorectal polyps in patients with familial adenomatous polyposis. Selective COX-2 inhibitors appear to be sufficiently safe to permit large-scale clinical testing and numerous clinical trials are currently under way to determine whether selective inhibitors of COX-2 are effective in the prevention and treatment of cancer.
机译:环氧合酶2(COX-2)是一种可诱导的前列腺素G / H合酶,在几种人类癌症中均过表达。在此,考虑了选择性COX-2抑制剂在预防和治疗癌症中的潜在用途。讨论了癌症中COX-2水平升高的机制,表明COX-2活性增加与肿瘤发生之间因果关系的关键数据以及COX-2的可能作用机制。在一项原理验证的临床试验中,使用选择性COX-2抑制剂塞来昔布治疗可减少家族性腺瘤性息肉病患者大肠息肉的数量。选择性COX-2抑制剂似乎足够安全,可以进行大规模的临床试验,并且目前正在进行大量临床试验,以确定COX-2的选择性抑制剂在预防和治疗癌症方面是否有效。

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