ADAM Metalloproteinases as Potential Drug Targets

被引:22
|
作者
Camodeca, Caterina [1 ]
Cuffaro, Doretta [1 ]
Nuti, Elisa [1 ]
Rossello, Armando [1 ]
机构
[1] Univ Pisa, Dept Pharm, Via Bonanno 6, I-56126 Pisa, Italy
关键词
Metalloendopeptidases; ectodomain shedding; adhesion molecules; hydroxamate inhibitors; zincbinding group; small molecules; NECROSIS-FACTOR-ALPHA; CELL-ADHESION MOLECULE; GROWTH-FACTOR RECEPTOR; AMYLOID PRECURSOR PROTEIN; CONVERTING-ENZYME TACE; TNF-ALPHA; CATALYTIC-ACTIVITY; DISINTEGRIN ADAM8; ECTODOMAIN CLEAVAGE; SECRETASE CLEAVAGE;
D O I
10.2174/0929867325666180326164104
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The ADAMs, together with ADAMTSs and snake venom metalloproteases (SVMPs), are members of the Adamalysin family. Differences in structural organization, functions and localization are known and their domains, catalytic or non-catalytic, show key roles in the substrate recognition and protease activity. Some ADAMs, as membrane-bound enzymes, show sheddase activity. Sheddases are key to modulation of functional proteins such as the tumor necrosis factor, growth factors, cytokines and their receptors, adhesion proteins, signaling molecules and stress molecules involved in immunity. These activities take part in the regulation of several physiological and pathological processes including inflammation, tumor growth, metastatic progression and infectious diseases. On these bases, some ADAMs are currently investigated as drug targets to develop new alternative therapies in many fields of medicine. This review will be focused on these aspects.
引用
收藏
页码:2661 / 2689
页数:29
相关论文
共 50 条
  • [31] Potential drug targets and treatment of schizophrenia
    Anil Kumar
    Monu Yadav
    Milind Parle
    Sameer Dhingra
    Dinesh K. Dhull
    Inflammopharmacology, 2017, 25 : 277 - 292
  • [32] Potential new drug targets for osteoporosis
    Chad Deal
    Nature Clinical Practice Rheumatology, 2009, 5 : 20 - 27
  • [33] IRESes: new potential drug targets?
    Ekblom, J
    DRUG DISCOVERY TODAY, 2001, 6 (24) : 1259 - 1260
  • [34] TRP channels as potential drug targets
    Wissenbach, U
    Niemeyer, BA
    Flockerzi, V
    BIOLOGY OF THE CELL, 2004, 96 (01) : 47 - 54
  • [35] Odorant receptors as potential drug targets
    Naressi, Rafaella G.
    Schechtman, Deborah
    Malnic, Bettina
    TRENDS IN PHARMACOLOGICAL SCIENCES, 2023, 44 (01) : 11 - 14
  • [36] INGs are potential drug targets for cancer
    Runyun Zhang
    Jianhua Jin
    Juanjuan Shi
    Yongzhong Hou
    Journal of Cancer Research and Clinical Oncology, 2017, 143 : 189 - 197
  • [37] Potential new drug targets for osteoporosis
    Deal, Chad
    NATURE CLINICAL PRACTICE RHEUMATOLOGY, 2009, 5 (01): : 20 - 27
  • [38] TRP Channels as Potential Drug Targets
    Moran, Magdalene M.
    ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, VOL 58, 2018, 58 : 309 - 329
  • [39] Potential new drug targets for osteoporosis
    Peralta Lopez, Maria Elena
    ACTUALIZACIONES EN OSTEOLOGIA, 2009, 5 (02) : 95 - 96
  • [40] Modified RNAs as potential drug targets
    Guenther, R
    Forrest, B
    Newman, W
    Malkiewicz, A
    Agris, PF
    ACTA BIOCHIMICA POLONICA, 1998, 45 (01) : 13 - 18