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

期刊

TRENDS IN PHARMACOLOGICAL SCIENCES
卷 40, 期 1, 页码 11-21

出版社

ELSEVIER SCIENCE LONDON
DOI: 10.1016/j.tips.2018.11.003

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资金

  1. Ministry of Education, Culture, Sports, Science and Technology (MEXT) [18H02605, 18K16994, 26462132, 26293055]
  2. Takeda Science Foundation
  3. Uehara Memorial Foundation
  4. Integrative Research Program of the Graduate School of Medical Science, Kitasato University
  5. Grants-in-Aid for Scientific Research [18K16994, 26462132] Funding Source: KAKEN

向作者/读者索取更多资源

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.

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