Literature DB >> 15882437

Quantification of tissue inhibitor of metalloproteinases 2 in plasma from healthy donors and cancer patients.

M B Larsen1, R W Stephens, N Brünner, H J Nielsen, L H Engelholm, I J Christensen, W G Stetler-Stevenson, G Høyer-Hansen.   

Abstract

Tissue inhibitor of metalloproteinases (TIMP)-2 is a highly conserved molecule, which binds both active and latent matrix metalloproteinase (MMP)-2. TIMP-2 is also involved in the activation of MMP-2 on the cell surface. A quantitative enzyme-linked immunosorbent assay (ELISA) was established and optimized for measurement of TIMP-2 in plasma. The capturing antibody in the ELISA was a monoclonal, while the detecting antibody was a chicken polyclonal antibody recognizing the native form of human TIMP-2. The levels of TIMP-2 were measured in ethylenediaminetetraacetic acid (EDTA) and citrate plasma from healthy donors. The median values were determined as 163 ng/ml (n = 186) with a range of 109-253 ng/ml for EDTA plasma and 139 ng/ml (n = 77) with a range of 95-223 ng/ml for citrate plasma. The TIMP-2 concentration in citrate plasma from 15 patients with advanced, stage IV breast cancer had a median value of 160 ng/ml, only slightly higher but statistically distinguishable from the level found in citrate plasma from the healthy donors. In addition, the TIMP-2 concentration in EDTA plasma from colorectal cancer patients revealed a significantly higher level in plasma from patients with Dukes stage A (P = 0.01) compared with patients with more advanced Dukes stages.

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Year:  2005        PMID: 15882437     DOI: 10.1111/j.1365-3083.2005.01585.x

Source DB:  PubMed          Journal:  Scand J Immunol        ISSN: 0300-9475            Impact factor:   3.487


  7 in total

1.  Systematic discovery of ectopic pregnancy serum biomarkers using 3-D protein profiling coupled with label-free quantitation.

Authors:  Lynn A Beer; Hsin-Yao Tang; Sira Sriswasdi; Kurt T Barnhart; David W Speicher
Journal:  J Proteome Res       Date:  2011-01-07       Impact factor: 4.466

2.  Analysis of the MMP-dependent and independent functions of tissue inhibitor of metalloproteinase-2 on the invasiveness of breast cancer cells.

Authors:  Logan A Walsh; Mario A Cepeda; Sashko Damjanovski
Journal:  J Cell Commun Signal       Date:  2012-01-08       Impact factor: 5.782

Review 3.  Tissue inhibitors of metalloproteinases in cell signaling: metalloproteinase-independent biological activities.

Authors:  William G Stetler-Stevenson
Journal:  Sci Signal       Date:  2008-07-08       Impact factor: 8.192

4.  Timp-2 binding with cellular MT1-MMP stimulates invasion-promoting MEK/ERK signaling in cancer cells.

Authors:  Nor Eddine Sounni; Dmitri V Rozanov; Albert G Remacle; Vladislav S Golubkov; Agnes Noel; Alex Y Strongin
Journal:  Int J Cancer       Date:  2010-03-01       Impact factor: 7.396

Review 5.  Sex-Related Differences of Matrix Metalloproteinases (MMPs): New Perspectives for These Biomarkers in Cardiovascular and Neurological Diseases.

Authors:  Alessandro Trentini; Maria Cristina Manfrinato; Massimiliano Castellazzi; Tiziana Bellini
Journal:  J Pers Med       Date:  2022-07-22

6.  Amnion-derived cellular cytokine solution: a physiological combination of cytokines for wound healing.

Authors:  David L Steed; Cathy Trumpower; Danelle Duffy; Charlotte Smith; Vivienne Marshall; Randall Rupp; Martin Robson
Journal:  Eplasty       Date:  2008-04-07

7.  TIMP-2 Interaction with MT1-MMP Activates the AKT Pathway and Protects Tumor Cells from Apoptosis.

Authors:  Cristina Valacca; Evelyne Tassone; Paolo Mignatti
Journal:  PLoS One       Date:  2015-09-02       Impact factor: 3.240

  7 in total

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