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非甾体抗炎药与化学预防。

NSAIDs and chemoprevention.

作者信息

Rao Chinthalapally V, Reddy Bandaru S

机构信息

Chemoprevention Program, Institute For Cancer Prevention, American Health Foundation-Cancer Center, 1 Dana Road, Valhalla, NY 10595, USA.

出版信息

Curr Cancer Drug Targets. 2004 Feb;4(1):29-42. doi: 10.2174/1568009043481632.

Abstract

Several epidemiological, clinical and experimental studies established nonsteroidal anti-inflammatory drugs (NSAIDs) as promising cancer chemopreventive agents. Long-term use of aspirin and other NSAIDs has been shown to reduce the risk of cancer of the colon and other gastrointestinal organs as well as of cancer of the breast, prostate, lung, and skin. Understanding the action of NSAIDs provides substantial insights into the mechanisms by which these unique agents regulate tumor cell growth and enable better strategies for prevention and treatment. NSAIDs restore normal apoptosis and reduce cell proliferation in human adenomatous colorectal polyps, experimental colonic tumors, and in various cancer cell lines that have lost critical genes required for normal function. NSAIDs, particularly selective cyclooxygenase-2 (COX-2) inhibitors such as celecoxib, have been shown to inhibit angiogenesis in cell culture and in rodent models of angiogenesis. Exploration of the multistep process of carcinogenesis has provided substantial insights into the mechanisms by which NSAIDs modulate these events. However, unresolved questions with regard to safety, efficacy, optimal treatment regimen, and mechanism of action currently limit the clinical application of NSAIDs to the prevention of polyposis in FAP patients. Moreover, the development of safe and effective NSAIDs for chemoprevention is complicated by the potential that rare, serious toxicity may offset the benefit of treatment with these drugs given to healthy individuals who have a low risk of developing the disease. Growing knowledge in this area has brought about innovative approaches using combine actions of NSAIDs with other agents that have different modes of action. It has also led to the development of nitric oxide-releasing NSAIDs, that induce tumor cell apoptosis and compensate for COX function, as a means of increasing efficacy and minimizing toxicity. There is growing optimism for the view that full exploration of the role of NSAIDs in the prevention and treatment of epithelial cancers will serve towards reducing of mortality and morbidity from various cancers.

摘要

多项流行病学、临床和实验研究证实,非甾体抗炎药(NSAIDs)是很有前景的癌症化学预防剂。长期服用阿司匹林和其他NSAIDs已显示可降低结肠癌和其他胃肠道器官癌症以及乳腺癌、前列腺癌、肺癌和皮肤癌的发病风险。了解NSAIDs的作用机制,有助于深入认识这些独特药物调节肿瘤细胞生长的方式,并有助于制定更好的预防和治疗策略。NSAIDs可恢复人类腺瘤性结直肠息肉、实验性结肠肿瘤以及各种因失去正常功能所需关键基因而发生癌变的细胞系中的正常细胞凋亡,并减少细胞增殖。NSAIDs,尤其是选择性环氧化酶-2(COX-2)抑制剂,如塞来昔布,已被证明在细胞培养和血管生成的啮齿动物模型中可抑制血管生成。对癌症发生多步骤过程的探索,为NSAIDs调节这些事件的机制提供了深入见解。然而,目前关于安全性、疗效、最佳治疗方案和作用机制等尚未解决的问题,限制了NSAIDs在临床中用于预防家族性腺瘤性息肉病(FAP)患者息肉形成的应用。此外,开发用于化学预防的安全有效的NSAIDs也很复杂,因为存在罕见但严重的毒性可能抵消给予患癌风险低的健康个体使用这些药物治疗益处的可能性。该领域不断增长的知识带来了创新方法,即联合使用NSAIDs与其他具有不同作用方式的药物。这也促使了一氧化氮释放型NSAIDs的开发,这类药物可诱导肿瘤细胞凋亡并补偿COX功能,以此提高疗效并将毒性降至最低。越来越多人乐观地认为,全面探索NSAIDs在预防和治疗上皮性癌症中的作用,将有助于降低各种癌症的死亡率和发病率。

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