CGRP/CGRP Receptor Antibodies: Potential Adverse Effects Due to Blockade of Neovascularization?

被引:27
作者
Majima, Masataka [1 ,2 ]
Ito, Yoshiya [1 ,2 ]
Hosono, Kanako [1 ,2 ]
Amano, Hideki [1 ,2 ]
机构
[1] Kitasato Univ, Sch Med, Dept Pharmacol, Sagamihara, Kanagawa 2520374, Japan
[2] Kitasato Univ, Grad Sch Med Sci, Dept Mol Pharmacol, Sagamihara, Kanagawa 2520374, Japan
关键词
GENE-RELATED PEPTIDE; ENDOTHELIAL GROWTH-FACTOR; ACTIVITY-MODIFYING PROTEIN-1; TUMOR-ASSOCIATED ANGIOGENESIS; CGRP RECEPTOR; DOUBLE-BLIND; MOLECULAR-MECHANISMS; CONTROLLED-TRIAL; MUCOSAL INJURY; MIGRAINE;
D O I
10.1016/j.tips.2018.11.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Migraine is a severe neurological disorder in which calcitonin gene-related peptide (CGRP) is a key molecule in pathophysiology. Neuronal system-derived CGRP enhances neovascularization in several important pathological conditions and sends a cue to the vascular system. In 2018, the FDA approved erenumab and fremanezumab, antibodies against CGRP receptor and CGRP, as the first new class of drugs for migraine. Treatment of migraine with these antibodies requires greatcare because neovascularization-related adverse effects may be induced in some patients. Here, we focus on enhancement of neovascularization by CGRP and discuss possible adverse effects resulting from blocking neovascularization. We also suggest that CGRP antibodies may also be used as novel antitumor agents by suppressing tumor-associated angiogenesis.
引用
收藏
页码:11 / 21
页数:11
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