Aminopeptidase-N/CD13 (EC 3.4.11.2) inhibitors: Chemistry, biological evaluations, and therapeutic prospects

被引:234
作者
Bauvois, B
Dauzonne, D
机构
[1] Inst Curie, CNRS, UMR176, Sect Rech, F-75248 Paris 05, France
[2] Univ Paris 05, INSERM, Unite 507, Hop Necker Enfants Malad, F-75015 Paris, France
关键词
aminopeptidase; ectoenzyme; natural inhibitor; synthetic inhibitor; bestatin; cancer; inflammation;
D O I
10.1002/med.20044
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
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/CID13 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.(c) 2005 Wiley Periodicals, Inc.
引用
收藏
页码:88 / 130
页数:43
相关论文
共 385 条
[1]  
Abe F, 1984, Jpn J Antibiot, V37, P589
[2]  
ABE F, 1984, GANN, V75, P89
[3]   ENHANCEMENT OF ANTITUMOR EFFECT OF CYTO-TOXIC AGENTS BY BESTATIN [J].
ABE, F ;
SHIBUYA, K ;
ASHIZAWA, J ;
TAKAHASHI, K ;
HORINISHI, H ;
MATSUDA, A ;
ISHIZUKA, M ;
TAKEUCHI, T ;
UMEZAWA, H .
JOURNAL OF ANTIBIOTICS, 1985, 38 (03) :411-414
[4]  
Abe T, 1998, Masui, V47, P151
[5]  
Aggarwal BB, 2003, ANTICANCER RES, V23, P363
[6]   Inhibition of growth and survival of human head and neck squamous cell carcinoma cells by curcumin via modulation of nuclear factor-κB signaling [J].
Aggarwal, S ;
Takada, Y ;
Singh, S ;
Myers, JN ;
Aggarwal, BB .
INTERNATIONAL JOURNAL OF CANCER, 2004, 111 (05) :679-692
[7]  
AHMAD S, 1990, J PHARMACOL EXP THER, V252, P643
[8]  
AHMAD S, 1992, J PHARMACOL EXP THER, V260, P1257
[9]   Leukotriene A4 hydrolase:: a critical role of glutamic acid-296 for the binding of bestatin [J].
Andberg, M ;
Wetterholm, A ;
Medina, JF ;
Haeggström, JZ .
BIOCHEMICAL JOURNAL, 2000, 345 :621-625
[10]   STUDIES CONCERNING ANTIBIOTIC ACTINONIN .7. MASS-SPECTRA OF ACTINONIN AND RELATED COMPOUNDS [J].
ANDERSON, NH ;
DEVLIN, JP ;
JONES, S ;
OLLIS, WD ;
THORPE, JE .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1975, (09) :852-857