Cyclooxygenase-2 promotes tumor growth and suppresses tumor immunity

被引:297
|
作者
Liu, Bing [1 ]
Qu, Liyan [2 ,3 ]
Yan, Shigui [1 ]
机构
[1] Zhejiang Univ, Sch Med, Affiliated Hosp 2, Dept Orthoped, Hangzhou 310009, Zhejiang, Peoples R China
[2] Zhejiang Univ, Sch Med, Affiliated Hosp 2, Clin Lab Ctr, Hangzhou 310009, Zhejiang, Peoples R China
[3] Binjiang Hosp Hangzhou, Clin Lab Ctr, Hangzhou, Zhejiang, Peoples R China
来源
CANCER CELL INTERNATIONAL | 2015年 / 15卷
关键词
COX-2; COX-inhibitors; EP; Innate immunity; Adaptive immunity; REGULATORY T-CELLS; PROSTANOID RECEPTORS; PHOSPHATIDYLINOSITOL; 3-KINASE; EXPRESSION; CANCER; EP4; PATHWAY; COLON; STIMULATION; MACROPHAGES;
D O I
10.1186/s12935-015-0260-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cyclooxygenase-2 (COX-2), an inducible form of the enzyme that catalyzes the first step in the synthesis of prostanoids, is associated with inflammatory diseases and carcinogenesis, which is suspected to promote angiogenesis and tissue invasion of tumors and resistance to apoptosis. Meanwhile, COX-2 contributes to immune evasion and resistance to cancer immunotherapy, which plays a crucial role in the innate and adaptive immune response. The activity of COX-2-PGE2-EP signal pathway can suppress Dendritic cells (DCs), natural killer (NK), T cells, type-1 immunity excluding type-2 immunity which promote tumor immune evasion. COX-2 and the prostaglandin cascade play important roles in the "inflammogenesis of cancer". In addition, COX-inhibitors can inhibit tumor immune evasion. Therefore, we can exert the COX-inhibitors to facilitate the patients to benefit from addition of COX-inhibitors to standard cytotoxic therapy.
引用
收藏
页数:6
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