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类二十烷酸信号通路在结直肠癌发生和发展中的作用:预防/干预的新方法。

Eicosanoid signalling pathways in the development and progression of colorectal cancer: novel approaches for prevention/intervention.

机构信息

Department of Surgery, Institute of Molecular Medicine, Trinity Health Sciences Centre, St James's Hospital, Trinity College Dublin, Dublin 8, Ireland.

出版信息

Cancer Metastasis Rev. 2011 Dec;30(3-4):363-85. doi: 10.1007/s10555-011-9324-x.

Abstract

Arachidonic acid metabolism through cyclooxygenase (COX), lipoxygenase (LOX) and cytochrome P-450 epoxygenase (EPOX) pathways leads to the generation of biologically active eicosanoids, including prostanoids, leukotrienes, hydroxyeicosatetraenoic acid, epoxyeicosatrienoic acid and hydroperoxyeicosatetraenoic acids. Eicosanoid expression levels vary during tumor development and progression of a range of malignancies, including colorectal cancer. The actions of these autocoids are also directly influenced by diet, as demonstrated by recent evidence for omega-3 fatty acids in colorectal cancer (CRC) prevention and/or treatment. Eicosanoids regulate CRC development and progression, while inhibition of these pathways has generally been shown to inhibit tumor growth/progression. A progressive sequence of colorectal cancer development has been identified, ranging from normal colon, to colitis, dysplasia, and carcinoma. While both COX and LOX inhibition are both promising candidates for colorectal cancer prevention and/or treatment, there is an urgent need to understand the mechanisms through which these signalling pathways mediate their effects on tumorigenesis. This will allow identification of safer, more effective strategies for colorectal cancer prevention and/or treatment. In particular, binding to/signalling through prostanoid receptors have recently been the subject of considerable interest in this area. In this review, we discuss the role of the eicosanoid signalling pathways in the development and progression of colorectal cancer. We discuss the effects of the eicosanoids on tumor cell proliferation, their roles in cell death induction, effects on angiogenesis, migration, invasion and their regulation of the immune response. Signal transduction pathways involved in these processes are also discussed. Finally, novel approaches targeting these arachidonic acid-derived eicosanoids (using pharmacological or natural agents) for chemoprevention and/or treatment of colorectal cancer are outlined.

摘要

花生四烯酸通过环氧化酶(COX)、脂氧合酶(LOX)和细胞色素 P-450 环氧合酶(EPOX)途径代谢,生成生物活性的类二十烷酸,包括前列腺素、白三烯、羟二十碳四烯酸、环氧二十碳三烯酸和氢过氧二十碳四烯酸。类二十烷酸的表达水平在多种恶性肿瘤(包括结直肠癌)的肿瘤发生和进展过程中发生变化。这些自体素的作用也受到饮食的直接影响,最近有证据表明ω-3 脂肪酸可预防和/或治疗结直肠癌(CRC)。类二十烷酸调节 CRC 的发生和发展,而抑制这些途径通常可抑制肿瘤生长/进展。已经确定了 CRC 发展的一系列渐进序列,从正常结肠到结肠炎、异型增生和癌。虽然 COX 和 LOX 抑制都是预防和/或治疗结直肠癌的有前途的候选药物,但迫切需要了解这些信号通路介导其对肿瘤发生影响的机制。这将允许为结直肠癌的预防和/或治疗确定更安全、更有效的策略。特别是,最近,与前列腺素受体的结合/信号转导已成为该领域的研究热点。在这篇综述中,我们讨论了类二十烷酸信号通路在结直肠癌发生和发展中的作用。我们讨论了类二十烷酸对肿瘤细胞增殖的影响、诱导细胞死亡的作用、对血管生成、迁移、侵袭的影响以及对免疫反应的调节作用。还讨论了参与这些过程的信号转导途径。最后,概述了针对这些花生四烯酸衍生的类二十烷酸(使用药理学或天然剂)进行化学预防和/或治疗结直肠癌的新方法。

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