Davies G L S
Department of Academic Biochemistry, Royal Marsden Hospital, Fulham Road, London SW3 6JJ, UK.
J Steroid Biochem Mol Biol. 2003 Sep;86(3-5):495-9. doi: 10.1016/j.jsbmb.2003.07.004.
This article discusses the role of cyclooxygenase-2 (COX-2) in the aetiology and progression of breast cancer. Renewed interest in chemoprevention using non-steroidal antiinflammatory drugs (NSAIDS) has come from observations that regular NSAID use is associated with a reduced incidence of some cancers including that of the breast. There is an increasing body of evidence supporting a role for COX-2 in breast cancer development and progression via effects on angiogenesis and apoptosis as well as via effects on intratumoural aromatase. New selective inhibitors of COX-2 are currently licensed for use in the treatment of arthritis and more recently in the chemoprevention of familial adenomatous polyposis (FAP). Large clinical chemoprevention studies with COX-2 inhibitors are already underway in colorectal cancer. Their role in breast cancer prevention and treatment has yet to be fully characterised, but merits further investigation.
本文讨论了环氧化酶-2(COX-2)在乳腺癌病因学及进展过程中的作用。对使用非甾体抗炎药(NSAIDs)进行化学预防重新产生兴趣,源于以下观察结果:经常使用NSAIDs与包括乳腺癌在内的某些癌症发病率降低有关。越来越多的证据支持COX-2通过对血管生成和细胞凋亡的影响以及对肿瘤内芳香化酶的影响,在乳腺癌发生和进展中发挥作用。新型COX-2选择性抑制剂目前已获许可用于治疗关节炎,最近还用于家族性腺瘤性息肉病(FAP)的化学预防。关于COX-2抑制剂的大型临床化学预防研究已在结直肠癌中展开。它们在乳腺癌预防和治疗中的作用尚未完全明确,但值得进一步研究。