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Open AccessJournal ArticleDOI

The ADAMs family of metalloproteases: multidomain proteins with multiple functions

Darren F. Seals, +1 more
- 01 Jan 2003 - 
- Vol. 17, Iss: 1, pp 7-30
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TLDR
This review will first discuss the properties of each of the domains of the ADAMs, then describe the involvement ofADAMs in selected biological processes, and highlight recent interesting findings suggesting roles for ADams in human disease.
Abstract
The ADAMs family of transmembrane proteins belongs to the zinc protease superfamily. Members of the family have a modular design, characterized by the presence of metalloprotease and integrin receptor-binding activities, and a cytoplasmic domain that in many family members specifies binding sites for various signal transducing proteins. The ADAMs family has been implicated in the control of membrane fusion, cytokine and growth factor shedding, and cell migration, as well as processes such as muscle development, fertilization, and cell fate determination. Pathologies such as inflammation and cancer also involve ADAMs family members. Excellent reviews covering various facets of the ADAMs literature-base have been published over the years and we recommend their examination (Black and White 1998; Schlondorff and Blobel 1999; Primakoff and Myles 2000; Evans 2001; Kheradmand and Werb 2002). In this review, we will first discuss the properties of each of the domains of the ADAMs. We will then go on to describe the involvement of ADAMs in selected biological processes. Then, we will highlight recent interesting findings suggesting roles for ADAMs in human disease. Finally, we look to the future and discuss some of the open issues in ADAMs function and regulation.

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ERBB receptors and cancer: the complexity of targeted inhibitors.

TL;DR: This work discusses the significance of these receptors as clinical targets, in particular the molecular mechanisms underlying response, and many ERBB inhibitors used in the clinic.
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ADAMs: key components in EGFR signalling and development

TL;DR: Research on ADAMs and their role in protein ectodomain shedding is emerging as a fertile ground for gathering new insights into the functional regulation of membrane proteins.
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The ADAM metalloproteinases.

TL;DR: The ADAM family are fundamental to many control processes in development and homeostasis, and unsurprisingly they are also linked to pathological states when their functions are dysregulated, including cancer, cardiovascular disease, asthma, Alzheimer’s disease.
Journal ArticleDOI

Association of the adam33 gene with asthma and bronchial hyperresponsiveness

Akaluck Thatayatikom, +1 more
- 01 Aug 2003 - 
TL;DR: The identification and characterization of ADAM33, a putative asthma susceptibility gene identified by positional cloning in an outbred population, should provide insights into the pathogenesis and natural history of this common disease.
Journal ArticleDOI

Distinct roles for ADAM10 and ADAM17 in ectodomain shedding of six EGFR ligands

TL;DR: This comprehensive evaluation of EG FR ligand shedding in a defined experimental system demonstrates that ADAMs have critical roles in releasing all EGFR ligands tested here, and has implications for designing novel inhibitors of EGFR-dependent tumors.
References
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Journal ArticleDOI

A metalloproteinase disintegrin that releases tumour-necrosis factor-α from cells

TL;DR: The results should facilitate the development of therapeutically useful inhibitors of TNF-α release, and they indicate that an important function of adamalysins may be to shed cell-surface proteins.
Journal ArticleDOI

The biology of chemokines and their receptors.

TL;DR: Some of the chemokines' biological effects in vivo and in vitro, described in the last few years are discussed, and the implications of these findings when considering chemokine receptors as therapeutic targets are discussed.
Journal ArticleDOI

Tissue inhibitors of metalloproteinases: evolution, structure and function.

TL;DR: The evolution of TIMPs, the recently elucidated high-resolution structures of TIMP and their complexes with metalloproteinases, and the results of mutational and other studies of structure-function relationships that have enhanced understanding of the mechanism and specificity of the inhibition of MMPs by TIMPs are highlighted.
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