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环氧化酶-2抑制剂作为辐射增强剂:肺癌治疗的新策略

COX-2 inhibitor as a radiation enhancer: new strategies for the treatment of lung cancer.

作者信息

Saha Debabrata, Pyo Hongryull, Choy Hak

机构信息

Department of Radiation Oncology, Vanderbilt University Medical Center, Nashville, Tennessee 37232-5671, USA.

出版信息

Am J Clin Oncol. 2003 Aug;26(4):S70-4. doi: 10.1097/01.COC.0000074161.92815.93.

DOI:10.1097/01.COC.0000074161.92815.93
PMID:12902860
Abstract

Lung cancer is one of the most common causes of cancer-related mortality throughout the world, and the incidence continues to increase. Smoking is the number one cause of lung cancer. Emerging data have implicated cyclooxygenase-2 (COX-2) and prostanoid production in the pathogenesis of lung carcinoma. In invasive lung tumors, COX-2 upregulation has been reported in up to 90% of cases. COX-2 upregulation is an early event in the development of non-small-cell lung cancer and may be integral to the development of new blood vessels and production of specific proteases that are critical to growth and spread of lung malignancies. COX-2 inhibitors are known to enhance the chemosensitivity in COX-2 overexpressing lung cancer cell lines. Recently, we have demonstrated that selective COX-2 inhibitors also enhance the effect of radiation in COX-2 overexpressed cells. Therefore, inhibitors of COX-2 in combination with chemoradiation therapy may be an alternative strategy that can be tested in clinical trials. The combination of COX-2 inhibitors and radiation suggest a complementary strategy to target angiogenesis while potentially minimizing the impact on quality of life. Currently, several groups are conducting clinical trials in cervix cancer, lung cancer, and brain tumors, using inhibitors of COX-2 in combination with chemotherapy and radiation therapy. These clinical trials will help to elucidate the role of this interesting class.

摘要

肺癌是全球癌症相关死亡的最常见原因之一,且发病率持续上升。吸烟是肺癌的首要病因。新出现的数据表明环氧合酶-2(COX-2)和前列腺素生成与肺癌发病机制有关。在浸润性肺肿瘤中,高达90%的病例报告有COX-2上调。COX-2上调是非小细胞肺癌发生过程中的早期事件,可能对于新血管生成以及对肺恶性肿瘤生长和扩散至关重要的特定蛋白酶的产生不可或缺。已知COX-2抑制剂可增强COX-2过表达肺癌细胞系的化疗敏感性。最近,我们已证明选择性COX-2抑制剂还可增强辐射对COX-2过表达细胞的作用。因此,COX-2抑制剂与放化疗联合使用可能是一种可在临床试验中进行检验的替代策略。COX-2抑制剂与放疗联合提示了一种靶向血管生成的互补策略,同时可能将对生活质量的影响降至最低。目前,有几个研究小组正在宫颈癌、肺癌和脑肿瘤中开展临床试验,使用COX-2抑制剂与化疗和放疗联合。这些临床试验将有助于阐明这类药物的作用。

相似文献

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COX-2 inhibitor as a radiation enhancer: new strategies for the treatment of lung cancer.环氧化酶-2抑制剂作为辐射增强剂:肺癌治疗的新策略
Am J Clin Oncol. 2003 Aug;26(4):S70-4. doi: 10.1097/01.COC.0000074161.92815.93.
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Expert Rev Anticancer Ther. 2004 Aug;4(4):543-60. doi: 10.1586/14737140.4.4.543.

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A cross-talk between NFAT and NF-κB pathways is crucial for nickel-induced COX-2 expression in Beas-2B cells.NFAT 和 NF-κB 通路之间的串扰对于镍诱导 Beas-2B 细胞中 COX-2 的表达至关重要。
Curr Cancer Drug Targets. 2011 Jun;11(5):548-59. doi: 10.2174/156800911795656001.
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Lung squamous cell carcinoma and adenocarcinoma cell lines use different mediators to induce comparable phenotypic and functional changes in human monocyte-derived dendritic cells.肺鳞状细胞癌细胞系和腺癌细胞系利用不同的介质在人单核细胞衍生的树突状细胞中诱导出相当的表型和功能变化。
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