Article
ADAM-17 predicts adverse outcome in patients with breast cancer.
Department of Pathology, Laboratory Medicine, Conway Institute, University College Dublin, Dublin 4, Ireland.
Annals of Oncology (impact factor:
6.43).
07/2008;
19(6):1075-81.
DOI:10.1093/annonc/mdm609
pp.1075-81
Source: PubMed
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Citations (0)
- Cited In (5)
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Dataset: Clinica Chimica Acta 2009 ADAMs review
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Chapter: EGFR-Ligand Signaling in Breast Cancer Metastasis: Recurring Developmental Themes
11/2011; , ISBN: 978-953-307-714-7 -
Article: The ADAMs family of proteases: new biomarkers and therapeutic targets for cancer?
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ABSTRACT: The ADAMs are transmembrane proteins implicated in proteolysis and cell adhesion. Forty gene members of the family have been identified, of which 21 are believed to be functional in humans. As proteases, their main substrates are the ectodomains of other transmembrane proteins. These substrates include precursor forms of growth factors, cytokines, growth factor receptors, cytokine receptors and several different types of adhesion molecules. Although altered expression of specific ADAMs has been implicated in different diseases, their best-documented role is in cancer formation and progression. ADAMs shown to play a role in cancer include ADAM9, ADAM10, ADAM12, ADAM15 and ADAM17. Two of the ADAMs, i.e., ADAM10 and 17 appear to promote cancer progression by releasing HER/EGFR ligands. The released ligands activate HER/EGFR signalling that culminates in increased cell proliferation, migration and survival. Consistent with a causative role in cancer, several ADAMs are emerging as potential cancer biomarkers for aiding cancer diagnosis and predicting patient outcome. Furthermore, a number of selective ADAM inhibitors, especially against ADAM10 and ADAM17, have been shown to have anti-cancer effects. At least one of these inhibitors is now undergoing clinical trials in patients with breast cancer.Clinical Proteomics 01/2011; 8(1):9.
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Keywords
140 invasive breast cancers
153 invasive breast cancers
active forms
breast cancer
breast cancer progression
cancer formation
cancer treatment
conventional prognostic factors
enzyme-linked immunosorbent assay
estrogen receptor status
growth factor-alpha
heparin-binding epidermal growth factor
low expression
low-grade tumors
lymph node metastasis
matrix metalloproteinase-like enzyme
new target
precursor
tumor necrosis factor-alpha
western blotting