4.7 Article

ADAM17, shedding, TACE as therapeutic targets

期刊

PHARMACOLOGICAL RESEARCH
卷 71, 期 -, 页码 19-22

出版社

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.phrs.2013.01.012

关键词

ADAM proteases; ADAM17; TACE; Shedding; IL-6 trans-signaling; TNF alpha

资金

  1. Deutsche Forschungsgemeinschaft, Bonn [SFB654, SFB841, SFB877]
  2. Cluster of Excellence 'Inflammation at Interfaces'

向作者/读者索取更多资源

ADAM17 has been molecularly cloned as the enzyme responsible for cleavage of the transmembrane protein TNF alpha (TNF alpha converting enzyme, TACE). Later it was realized that ADAM17 was also responsible for the processing of cell adhesion proteins, cytokine and growth factor receptors and many ligands of the EGF receptor. Since TNF alpha is a target of anti-inflammatory therapies, it was speculated that inhibition of ADAM17 might be a therapeutic strategy in the treatment of inflammation or inflammation associated cancer. Meanwhile it has been recognized that ADAM17 governs many vital functions in the body and loss of ADAM17 leads to severe defects in the skin and to high susceptibility of the intestine to inflammation. Here I summarize data on the physiologic role of ADAM17 and the feasibility of specific blockade of this enzyme. (C) 2013 Elsevier Ltd. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据