The influence of Cox-2 and bioactive lipids on hematological cancers.

Sesquile Ramon, Collynn F Woeller, Richard P Phipps
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引用次数: 16

Abstract

Inflammation is implicated in the progression of multiple types of cancers including lung, colorectal, breast and hematological malignancies. Cyclooxygenases (Cox) -1 and -2 are important enzymes involved in the regulation of inflammation. Elevated Cox-2 expression is associated with a poor cancer prognosis. Hematological malignancies, which are among the top 10 most predominant cancers in the USA, express high levels of Cox-2. Current therapeutic approaches against hematological malignances are insufficient as many patients develop resistance or relapse. Therefore, targeting Cox-2 holds promise as a therapeutic approach to treat hematological malignancies. NSAIDs and Cox-2 selective inhibitors are anti-inflammatory drugs that decrease prostaglandin and thromboxane production while promoting the synthesis of specialized proresolving mediators. Here, we review the evidence regarding the applicability of NSAIDs, such as aspirin, as well as Cox-2 specific inhibitors, to treat hematological malignancies. Furthermore, we discuss how FDA-approved Cox inhibitors can be used as anti-cancer drugs alone or in combination with existing chemotherapeutic treatments.

Cox-2和生物活性脂质对血液学癌症的影响。
炎症与多种类型癌症的进展有关,包括肺癌、结直肠癌、乳腺癌和血液系统恶性肿瘤。环氧合酶(Cox) -1和-2是参与炎症调节的重要酶。Cox-2表达升高与癌症预后不良相关。血液恶性肿瘤是美国十大最主要的癌症之一,它表达高水平的Cox-2。目前针对血液系统恶性肿瘤的治疗方法是不够的,因为许多患者出现耐药性或复发。因此,靶向Cox-2有望成为治疗血液系统恶性肿瘤的一种治疗方法。非甾体抗炎药和Cox-2选择性抑制剂是一种消炎药,可减少前列腺素和凝血素的产生,同时促进专门促生介质的合成。在这里,我们回顾了关于非甾体抗炎药(如阿司匹林)和Cox-2特异性抑制剂治疗血液恶性肿瘤的适用性的证据。此外,我们还讨论了fda批准的Cox抑制剂如何单独用作抗癌药物或与现有化疗药物联合使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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