Literature DB >> 17920749

Emerging roles of ADAM and ADAMTS metalloproteinases in cancer.

N Rocks1, G Paulissen, M El Hour, F Quesada, C Crahay, M Gueders, J M Foidart, A Noel, D Cataldo.   

Abstract

A disintegrin and metalloproteinases (ADAMs) are a recently discovered family of proteins that share the metalloproteinase domain with matrix metalloproteinases (MMPs). Among this family, structural features distinguish the membrane-anchored ADAMs and the secreted ADAMs with thrombospondin motifs referred to as ADAMTSs. By acting on a large panel of membrane-associated and extracellular substrates, they control several cell functions such as adhesion, fusion, migration and proliferation. The current review addresses the contribution of these proteinases in the positive and negative regulation of cancer progression as mainly mediated by the regulation of growth factor activities and integrin functions.

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Year:  2007        PMID: 17920749     DOI: 10.1016/j.biochi.2007.08.008

Source DB:  PubMed          Journal:  Biochimie        ISSN: 0300-9084            Impact factor:   4.079


  90 in total

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4.  Variability in melanoma metalloproteinase expression profiling.

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Journal:  J Biomol Tech       Date:  2010-12

5.  Proteolytic Activity Matrix Analysis (PrAMA) for simultaneous determination of multiple protease activities.

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Review 6.  Molecular background of the regional lymph node metastasis of gastric cancer.

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Review 7.  The roles of ADAMTS in angiogenesis and cancer.

Authors:  Yi Sun; Jintuan Huang; Zuli Yang
Journal:  Tumour Biol       Date:  2015-04-28

Review 8.  The oncogene ERG: a key factor in prostate cancer.

Authors:  P Adamo; M R Ladomery
Journal:  Oncogene       Date:  2015-04-27       Impact factor: 9.867

9.  Molecular consequences of altered neuronal cholesterol biosynthesis.

Authors:  Zeljka Korade; Anne K Kenworthy; Károly Mirnics
Journal:  J Neurosci Res       Date:  2009-03       Impact factor: 4.164

10.  ADAM10 regulates proliferation, invasion, and chemoresistance of bladder cancer cells.

Authors:  Lin Fu; Nan Liu; Yong Han; Chengyao Xie; Qingchang Li; Enhua Wang
Journal:  Tumour Biol       Date:  2014-06-18
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