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Role of cyclooxygenase-2 in colorectal cancer.

机译:环氧合酶2在大肠癌中的作用。

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摘要

Cyclooxygenase-2 (COX-2) is an inducible enzyme that regulates prostaglandin synthesis and is overexpressed at sites of inflammation and in several epithelial cancers. Recently, a causal link for COX-2 in epithelial tumorigenesis was shown in genetically-manipulated animal models of colon and breast carcinoma. Data indicate that COX-2 is involved in the regulation of apoptosis, angiogenesis, and tumor cell invasiveness, which appear to contribute to its effects on tumorigenesis. Multiple studies have shown that nonselective COX and selective COX-2 inhibitors effectively prevent experimental colon cancer. Furthermore, sulindac and the selective COX-2 inhibitor celecoxib were shown to regress colorectal polyps in patients with familial adenomatous polyposis. Although the exact anti-tumor mechanisms of these agents await further study, data indicate that both COX-dependent and COX-independent mechanisms may be important. In this review, the association between COX-2 and colorectal tumorigenesis and potential mechanisms of this effect are discussed. Additionally, evidence supporting the role of NSAIDs and selective COX-2 inhibitors for the prevention and treatment of human colorectal cancer is reviewed.
机译:环氧合酶2(COX-2)是一种可调控前列腺素合成的诱导酶,在炎症部位和某些上皮癌中过表达。最近,在结肠和乳腺癌的基因操纵动物模型中显示了COX-2在上皮肿瘤发生中的因果关系。数据表明,COX-2参与细胞凋亡,血管生成和肿瘤细胞侵袭性的调节,似乎有助于其对肿瘤发生的作用。多项研究表明,非选择性COX和选择性COX-2抑制剂可有效预防实验性结肠癌。此外,舒林酸和选择性COX-2抑制剂塞来昔布被证明可以使家族性腺瘤性息肉病患者的结肠直肠息肉消退。尽管这些药物的确切抗肿瘤机制有待进一步研究,但数据表明,COX依赖性和COX依赖性机制均可能很重要。在这篇综述中,讨论了COX-2与结直肠肿瘤发生之间的关联以及这种作用的潜在机制。另外,综述了支持NSAID和选择性COX-2抑制剂在预防和治疗人类结直肠癌中作用的证据。

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