Targeting glia for bone cancer pain

被引:45
|
作者
Zhou, Ya-Qun [1 ,2 ]
Liu, Zheng [3 ]
Liu, Hui-Quan [4 ]
Liu, Dai-Qiang [1 ,2 ]
Chen, Shu-Ping [1 ,2 ]
Ye, Da-Wei [4 ]
Tian, Yu-Ke [1 ,2 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, Res Ctr Anesthesiol & Pain Med, Wuhan, Peoples R China
[2] Huazhong Univ Sci & Technol, Tongji Hosp, Dept Anesthesiol & Pain Med, Tongji Med Coll, Wuhan, Peoples R China
[3] Huazhong Univ Sci & Technol, Dept Urol, Tongji Hosp, Tongji Med Coll, Wuhan, Peoples R China
[4] Huazhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, Ctr Canc, Wuhan, Peoples R China
关键词
Therapeutic target; microglia; astrocyte; bone cancer pain; TUMOR-NECROSIS-FACTOR; TOLL-LIKE RECEPTOR; GENE-RELATED PEPTIDE; ACTIVATED PROTEIN-KINASE; PLACEBO-CONTROLLED TRIAL; DORSAL-HORN NEURONS; LOW-BACK-PAIN; NF-KAPPA-B; RAT MODEL; SPINAL-CORD;
D O I
10.1080/14728222.2016.1214716
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Bone cancer pain (BCP) remains to be a clinical challenge with limited pharmaceutical interventions. Therefore, novel therapeutic targets for the management of BCP are in desperate need. Recently, a growing body of evidence has suggested that glial cells may play a pivotal role in the pathogenesis of BCP.Areas covered: This review summarizes the recent progress in the understanding of glia in BCP and reveals the potential therapeutic targets in glia for BCP treatment.Expert opinion: Pharmacological interventions inhibiting the activation of glial cells, suppressing glia-derived proinflammatory cytokines, cell surface receptors, and the intracellular signaling pathways may be beneficial for the pain management of advanced cancer patients. However, these pharmacological interventions should not disrupt the normal function of glia cells since they play a vital supportive and protective role in the central nervous system.
引用
收藏
页码:1365 / 1374
页数:10
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