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脂氧合酶和环氧化酶途径与结直肠癌预防

Lipoxygenase and Cyclooxygenase Pathways and Colorectal Cancer Prevention.

作者信息

Rao Chinthalapally V, Janakiram Naveena B, Mohammed Altaf

机构信息

Center for Cancer Prevention and Drug Development, Medical Oncology, Department of Medicine, PC Stephenson Cancer Center, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, USA.

出版信息

Curr Colorectal Cancer Rep. 2012 Dec;8(4):316-324. doi: 10.1007/s11888-012-0146-1.

Abstract

Colorectal cancer is one of the commonest malignancies in both men and women. In spite of significant progress in screening and in surgical and therapeutic interventions, colorectal cancer (CRC) is still a major public health problem. Accumulating evidence suggests that targeting inflammatory pathways may provide protection against the development of CRC. Eicosanoids derived from the enzymes cyclooxygenase (COX) and lipoxygenase (LOX) may contribute to CRC carcinogenesis. Approaches for targeting COX-1 and COX-2 with traditional nonsteroidal anti-inflammatory agents or targeting COX-2 with specific inhibitors are highly successful at the preclinical and clinical levels; however, large-scale clinical applicability of these agents is limited owing to unwanted side effects. Emerging studies suggests that 5-LOX-derived leukotrienes may contribute to colon tumor development and risk of thrombotic events. Thus, developing drugs that target both 5-LOX and COX-2 may provide a safer strategy. In this review, we discuss evidence for the involvement of 5-LOX in colon tumor development and targeting 5-LOX and COX-2 with synthetic and naturally occurring agents for CRC prevention.

摘要

结直肠癌是男性和女性中最常见的恶性肿瘤之一。尽管在筛查以及手术和治疗干预方面取得了重大进展,但结直肠癌(CRC)仍然是一个主要的公共卫生问题。越来越多的证据表明,针对炎症途径可能会预防CRC的发生。由环氧化酶(COX)和脂氧合酶(LOX)产生的类花生酸可能会促进CRC的致癌作用。在临床前和临床水平上,使用传统非甾体抗炎药靶向COX-1和COX-2或使用特异性抑制剂靶向COX-2的方法非常成功;然而,由于不良副作用,这些药物的大规模临床应用受到限制。新出现的研究表明,5-LOX衍生的白三烯可能会促进结肠肿瘤的发展和血栓形成事件的风险。因此,开发同时靶向5-LOX和COX-2的药物可能会提供一种更安全的策略。在这篇综述中,我们讨论了5-LOX参与结肠肿瘤发展的证据,以及使用合成和天然药物靶向5-LOX和COX-2预防CRC的情况。

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