Literature DB >> 19075595

ADAM proteins - therapeutic potential in cancer.

Xinjie Lu1, Dong Lu, Mike Scully, Vijay Kakkar.   

Abstract

The A Disintegrin And Metalloprotease (ADAM) proteins belong to the metzincin-superfamily of Zn-dependent metalloproteinases that shed the extracellular domains of membrane-bound growth factors, cytokines and their receptors. The latter play a central role in cell signaling and contribute a potential target in cancer therapy. Of particular interest are the ErBB/HER family of growth factor receptors associated with elevated intrinsic tyrosine kinase activity. Overexpression of ADAMs and cell signaling components have also been implicated in the development and progression of a variety of tumor types. Emerging evidence has suggested that the ADAM proteins are involved in tumour cell proliferation, in angiogenesis as well as metastasis. Therefore, strategies targeting ADAMs may constitute an important target for the design of cancer drugs. The review will focus on current understanding of the role of ADAM in the physiological and pathological functions associated with cancer. It is the intention of the review to provide insights which may assist in the development of ADAM-based approaches for the treatment of human cancers.

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Year:  2008        PMID: 19075595     DOI: 10.2174/156800908786733478

Source DB:  PubMed          Journal:  Curr Cancer Drug Targets        ISSN: 1568-0096            Impact factor:   3.428


  24 in total

1.  Transcriptional control of PAX4-regulated miR-144/451 modulates metastasis by suppressing ADAMs expression.

Authors:  J Zhang; X Qin; Q Sun; H Guo; X Wu; F Xie; Q Xu; M Yan; J Liu; Z Han; W Chen
Journal:  Oncogene       Date:  2014-08-25       Impact factor: 9.867

Review 2.  Emerging principles in protease-based drug discovery.

Authors:  Marcin Drag; Guy S Salvesen
Journal:  Nat Rev Drug Discov       Date:  2010-09       Impact factor: 84.694

3.  TGF-β1 promotes motility and invasiveness of glioma cells through activation of ADAM17.

Authors:  Yong Lu; Feng Jiang; Xuguang Zheng; Mark Katakowski; Benjamin Buller; Shing-Shun Tony To; Michael Chopp
Journal:  Oncol Rep       Date:  2011-02-24       Impact factor: 3.906

Review 4.  Inhibition of MMPs and ADAM/ADAMTS.

Authors:  Charles J Malemud
Journal:  Biochem Pharmacol       Date:  2019-02-28       Impact factor: 5.858

5.  Identification and functional analysis of endothelial tip cell-enriched genes.

Authors:  Raquel del Toro; Claudia Prahst; Thomas Mathivet; Geraldine Siegfried; Joshua S Kaminker; Bruno Larrivee; Christiane Breant; Antonio Duarte; Nobuyuki Takakura; Akiyoshi Fukamizu; Josef Penninger; Anne Eichmann
Journal:  Blood       Date:  2010-08-12       Impact factor: 22.113

6.  Gallic acid suppresses cell viability, proliferation, invasion and angiogenesis in human glioma cells.

Authors:  Yong Lu; Feng Jiang; Hao Jiang; Kalina Wu; Xuguang Zheng; Yizhong Cai; Mark Katakowski; Michael Chopp; Shing-Shun Tony To
Journal:  Eur J Pharmacol       Date:  2010-06-08       Impact factor: 4.432

7.  Clinical significance of ADAM10 expression in laryngeal carcinoma.

Authors:  Bo You; Miao Gu; Xiaolei Cao; Xingyu Li; Si Shi; Ying Shan; Yiwen You
Journal:  Oncol Lett       Date:  2016-12-28       Impact factor: 2.967

8.  Molecular profiling of ADAM12 and ADAM17 genes in human malignant melanoma.

Authors:  Natalia Cireap; Diana Narita
Journal:  Pathol Oncol Res       Date:  2013-05-06       Impact factor: 3.201

9.  Inhibiting adenoid cystic carcinoma cells growth and metastasis by blocking the expression of ADAM 10 using RNA interference.

Authors:  Qin Xu; Xiuming Liu; Wantao Chen; Zhiyuan Zhang
Journal:  J Transl Med       Date:  2010-12-20       Impact factor: 5.531

10.  MiR-145 reduces ADAM17 expression and inhibits in vitro migration and invasion of glioma cells.

Authors:  Yong Lu; Michael Chopp; Xuguang Zheng; Mark Katakowski; Benjamin Buller; Feng Jiang
Journal:  Oncol Rep       Date:  2012-10-17       Impact factor: 3.906

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