Aminopeptidase-N/CD13 (EC 3.4.11.2) inhibitors: Chemistry, biological evaluations, and therapeutic prospects
Autor: | Brigitte Bauvois, Daniel Dauzonne |
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Přispěvatelé: | Signalisation cellulaire, dynamique circulatoire et athérosclérose précoce (SCDCAP), Université Pierre et Marie Curie - Paris 6 (UPMC)-Centre National de la Recherche Scientifique (CNRS) |
Rok vydání: | 2005 |
Předmět: |
MESH: Hydroxamic Acids
natural inhibitor Angiogenesis medicine.medical_treatment Pharmacology Hydroxamic Acids 01 natural sciences MESH: Tyrosine 0302 clinical medicine MESH: Curcumin Drug Discovery MESH: Animals Disulfides Receptor Neprilysin 0303 health sciences aminopeptidase MESH: Protease Inhibitors MESH: Neprilysin Chemistry MESH: Antigens CD13 General Medicine Transmembrane protein 3. Good health 030220 oncology & carcinogenesis MESH: Oligopeptides Molecular Medicine medicine.symptom Pentacyclic Triterpenes Oligopeptides MESH: Neovascularization Physiologic hormones hormone substitutes and hormone antagonists Cell type bestatin Curcumin animal structures Neovascularization Physiologic Inflammation ectoenzyme [SDV.BC]Life Sciences [q-bio]/Cellular Biology CD13 Antigens Article 03 medical and health sciences Immune system Leucine MESH: Cell Proliferation synthetic inhibitor medicine cancer Animals Humans Protease Inhibitors MESH: Disulfides Secretion Betulinic Acid Cell Proliferation 030304 developmental biology MESH: Humans Protease 010405 organic chemistry Cell growth MESH: Triterpenes Triterpenes 0104 chemical sciences MESH: Leucine inflammation Tyrosine |
Zdroj: | Med Res Rev Med Res Rev, 2006, 26 (1), pp.88-130. ⟨10.1002/med.20044⟩ Medicinal Research Reviews |
ISSN: | 1098-1128 0198-6325 |
DOI: | 10.1002/med.20044 |
Popis: | Aminopeptidase N (APN)/CD13 (EC 3.4.11.2) is a transmembrane protease present in a wide variety of human tissues and cell types (endothelial, epithelial, fibroblast, leukocyte). APN/CD13 expression is dysregulated in inflammatory diseases and in cancers (solid and hematologic tumors). APN/CD13 serves as a receptor for coronaviruses. Natural and synthetic inhibitors of APN activity have been characterized. These inhibitors have revealed that APN is able to modulate bioactive peptide responses (pain management, vasopressin release) and to influence immune functions and major biological events (cell proliferation, secretion, invasion, angiogenesis). Therefore, inhibition of APN/CD13 may lead to the development of anti‐cancer and anti‐inflammatory drugs. This review provides an update on the biological and pharmacological profiles of known natural and synthetic APN inhibitors. Current status on their potential use as therapeutic agents is discussed with regard to toxicity and specificity. © 2005 Wiley Periodicals, Inc. Med Res Rev |
Databáze: | OpenAIRE |
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