The regulation and importance of monocyte chemoattractant protein-1

被引:249
作者
Bianconi, Vanessa [1 ]
Sahebkar, Amirhossein [2 ]
Atkin, Stephen L. [3 ]
Pirro, Matteo [1 ]
机构
[1] Univ Perugia, Hosp Santa Maria Misericordia, Unit Internal Med, Dept Med, Perugia, Italy
[2] Mashhad Univ Med Sci, Biotechnol Res Ctr, Mashhad, Iran
[3] Weill Cornell Med Qatar, Doha, Qatar
关键词
atherosclerosis; cancer; CC chemokine receptor 2; inflammation; monocyte chemoattractant protein; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; CHEMOKINE RECEPTOR; MACROPHAGE INFILTRATION; METABOLIC SYNDROME; PANCREATIC-CANCER; MCP-1; CHEMOKINE; CURCUMIN; EXPRESSION; TUMOR; CCR2;
D O I
10.1097/MOH.0000000000000389
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Purpose of review Monocyte chemoattractant protein (MCP)-1, a chemokine regulating monocyte chemotaxis and T-lymphocyte differentiation by binding to the CC chemokine receptor 2 (CCR2), plays a crucial role in the pathogenesis of inflammatory diseases, atherosclerosis and cancer. This review summarizes the current knowledge on the regulation and importance of the MCP-1/CCR2 axis, focusing on the therapeutic potential of its inhibition. Recent findings Differential modulation of MCP-1 and CCR2 lead to downstream activation pathways, pathogenetic to differing disease conditions characterized by dysregulated monocyte/macrophage tissue recruitment. Pharmacological targeting of the MCP-1/CCR2 axis has led to selective MCP-1/CCR2 antagonists that have now entered phase I/II clinical trials for the treatment of inflammatory diseases, atherosclerosis and cancer. The pleiotropic nonselective MCP-1/CCR2 inhibition by current pharmacological agents is thought to contribute to their anti-inflammatory and antiatherosclerotic effects that is also seen for nutraceutical compounds such as curcumin. Summary MCP-1 has a critical role in regulating chemotaxis both in health and disease, with increasing interest in its pharmacological inhibition. However, the therapeutic efficacy and safety of targeting the MCP-1/CCR2 axis is still in evolution.
引用
收藏
页码:44 / 51
页数:8
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