摘要
趋化因子及其受体与肿瘤的发生、发展过程密切相关,针对趋化因子受体的抗体及小分子拮抗剂可能具有抗肿瘤作用。然而肿瘤微环境中的趋化因子为数众多,相互关系极其复杂,有必要确立针对趋化因子网络的多靶点调控策略。DARC、D6、CCX-CKR、Evasins、US28等趋化因子结合蛋白(CKBP)可以同时捕获肿瘤微环境中的多种促肿瘤性趋化因子,管控肿瘤细胞的生物学行为,已经或正在呈现出广阔的应用前景。
Chemokines and chemokine receptors are associated with the growth, metastasis of tumor cells. Antibodies or small moleculer antagonists against for ehemokine receptors should be used as anti-cancer drugs. However, the re- cent failures in the clinical trials of some single target antagonists suggest that chemokine network in tumor mieroenvi- ronment is very complicated. Obviously, multi-targets regulation strategy for chemokine network is indispensable. Chemokine-binding proteins (CKBP), including DARC, D6 and CCX-CKR, Evasins from ticks, US28 from virus, may control the biological behavior of tumor cells, by sequestrating pro-tumor ehemokines simultaneously.
出处
《延安大学学报(医学科学版)》
2013年第3期1-7,16,共8页
Journal of Yan'an University:Medical Science Edition
基金
国家自然科学基金(No.81172506)
上海市乳腺肿瘤重点实验室资助项目(No.12DZ2260100)