| Literature DB >> 30502971 |
Masataka Majima1, Yoshiya Ito2, Kanako Hosono2, Hideki Amano2.
Abstract
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 great care 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.Entities:
Keywords: angiogenesis; antibody; calcitonin gene-related peptide; lymphangiogenesis; migraine; neuronal system
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Year: 2018 PMID: 30502971 DOI: 10.1016/j.tips.2018.11.003
Source DB: PubMed Journal: Trends Pharmacol Sci ISSN: 0165-6147 Impact factor: 14.819