Liu Bing, Qu Liyan, Yan Shigui
Department of Orthopedics, 2nd Affiliated Hospital, School of Medicine, Zhejiang University, #88 Jie Fang Road, 310009 Hangzhou, Zhejiang People's Republic of China.
Clinical Laboratory Centre, 2nd Affiliated Hospital, School of Medicine, Zhejiang University, #88 Jie Fang Road, 310009 Hangzhou, Zhejiang People's Republic of China ; Clinical Laboratory Centre, Binjiang Hospital of Hangzhou, Hangzhou, Zhejiang People's Republic of China.
Cancer Cell Int. 2015 Nov 5;15:106. doi: 10.1186/s12935-015-0260-7. eCollection 2015.
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.
环氧化酶-2(COX-2)是一种可诱导形式的酶,催化前列腺素合成的第一步,与炎症性疾病和致癌作用相关,据怀疑它会促进肿瘤的血管生成、组织侵袭以及对细胞凋亡的抵抗。同时,COX-2有助于免疫逃逸和对癌症免疫疗法的抵抗,而这在先天和适应性免疫反应中起着关键作用。COX-2-PGE2-EP信号通路的活性可抑制树突状细胞(DCs)、自然杀伤细胞(NK)、T细胞,即抑制1型免疫(不包括促进肿瘤免疫逃逸的2型免疫)。COX-2和前列腺素级联反应在“癌症炎症发生”中起重要作用。此外,COX抑制剂可抑制肿瘤免疫逃逸。因此,我们可以使用COX抑制剂,以便让患者从在标准细胞毒性疗法中添加COX抑制剂中获益。