COX‐2抑制剂和结直肠癌的化学预防

J. Tsu, J. Ho
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引用次数: 1

摘要

尽管最近在对其分子遗传学的理解方面取得了进展,但结直肠癌仍然是全球癌症死亡的主要原因之一。有可能阻止或逆转癌变过程的化合物正在被研究作为可能的化学保护剂。在这些药物中,非甾体抗炎药(NSAID)已被证明可以显著降低结直肠癌的风险。新一代非甾体抗炎药对同工酶环加氧酶2 (COX-2)具有特异性抑制作用,最近已被引入临床使用,目的是减少不良反应。使用这些COX-2抑制剂的研究已经通过各种机制证明了显著的化学预防作用。在一项短期随机对照试验中,这些COX-2抑制剂在家族性腺瘤性息肉病(FAP)患者中也显示出令人鼓舞的结果。然而,在常规临床使用这类药物用于治疗FAP患者和其他高危人群之前,还需要进一步的研究。中文摘要图中文摘要
本文章由计算机程序翻译,如有差异,请以英文原文为准。
COX‐2 inhibitors and colorectal cancer chemoprevention
Despite recent advances in the understanding of its molecular genetics, colorectal cancer remains one of the worldwide leading causes of cancer death. Compounds with the potential to halt or reverse the carcinogenesis process are being studied as possible chemoprotective agents. Among these agents, non-steroidal anti-inflammatory drugs (NSAID) have been shown to significantly reduce colorectal cancer risk. A new generation of NSAID with specific inhibition towards the isozyme cyclo-oxygenase 2 (COX-2) has been introduced recently to clinical use with the aim of causing fewer adverse effects. Studies using these COX-2 inhibitors have demonstrated a significant chemopreventive effect via various mechanisms. In a short-term randomised controlled trial, these COX-2 inhibitors have also shown encouraging results in patients with familial adenomatous polyposis (FAP). However, further studies are necessary before routine clinical use of this class of agents can be used in the management of FAP patients and other at-risk population groups. Chinese Abstract Figure Chinese Abstract.
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