The cyclooxygenase-2/thromboxane A2 pathway: a bridge from rheumatoid arthritis to lung cancer?

被引:33
作者
Huang, Qing-Chun [1 ]
Huang, Run-Yue [1 ]
机构
[1] Guangzhou Univ Chinese Med, Affiliated Hosp 2, Dept Rheumatol, Guangdong Prov Hosp Chinese Med, Guangzhou 510006, Guangdong, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Rheumatoid arthritis; Lung cancer; Cyclooxygenase-2; Thromboxane A2; Auto-regulatory feedback loop; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; THROMBOXANE SYNTHASE; PROSTAGLANDIN E-2; CYCLO-OXYGENASE-2; INHIBITORS; CELL-PROLIFERATION; PROSTANOID RELEASE; UP-REGULATION; EXPRESSION; RISK; RECEPTOR;
D O I
10.1016/j.canlet.2014.08.024
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Patients with rheumatoid arthritis (RA) appear to be at a higher risk of lung cancer (LC). Although the connection between RA and LC has been an active area of research for many years, the molecular pathogenesis of the disease process remains unclear. The cyclooxygenase (COX)-2/thromboxane A2 (TxA2) pathway has been shown to play a potential role in LC development through an auto-regulatory feedback loop. An increased level of TxA2 has been found in RA patients, and intriguingly, the positive feedback loop for the COX-2/TxA2 pathway was shown to have a potential function in RA fibroblast-like synoviocytes (RA-FLS). Thus, the molecular basis of LC development in patients with RA has been at least in partly described. It is possible that COX-2-derived TxA2 could be monitored for the early detection of LC in RA patients, and targeting this molecular pathway may decrease the risk of LC in patients with RA. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:28 / 32
页数:5
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