Literature DB >> 20486866

Metalloproteinase binding proteins: WO2009097397.

Yoshifumi Itoh1.   

Abstract

MMPs are a group of metalloendopeptidases whose major role is in extracellular matrix (ECM) catabolism under physiological and pathological conditions. ECM catabolism is often associated with different diseases, and accumulated studies support the causal relationship between MMPs and different diseases especially with cancer and arthritis. Therefore, MMPs have been considered as therapeutic target molecules. However, multiple failures of MMP inhibitor drugs in clinical trials from late 1990s to early 2000s resulted in the consideration that wide inhibitory spectrum inhibitors of metalloproteinases may not be desirable for treatment of diseases. On the other hand, developing low molecular mass selective inhibitor(s) targeting the active site is not a very easy task. One way to overcome this problem is to develop biologic inhibitors, namely antibodies. In this patent application, Dyax Corp. reported that a binding protein (such as an antibody) against metalloproteinases, especially membrane-type 1 MMP (MMP-14) can be used as a therapeutic drug against different diseases including cancer. They succeeded in generating a selective MMP-14 inhibitory antibody with a K(i) of 0.6 nM, which showed significant suppression of different tumour growth in mice. Further development of such an antibody as a drug may fulfil an unmet area of disease treatment targeting uncontrolled cell invasion and tissue destruction.

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Year:  2010        PMID: 20486866      PMCID: PMC2912531          DOI: 10.1517/13543776.2010.488221

Source DB:  PubMed          Journal:  Expert Opin Ther Pat        ISSN: 1354-3776            Impact factor:   6.674


  35 in total

1.  Impaired endochondral ossification and angiogenesis in mice deficient in membrane-type matrix metalloproteinase I.

Authors:  Z Zhou; S S Apte; R Soininen; R Cao; G Y Baaklini; R W Rauser; J Wang; Y Cao; K Tryggvason
Journal:  Proc Natl Acad Sci U S A       Date:  2000-04-11       Impact factor: 11.205

2.  Expression of membrane-type 1 matrix metalloproteinase (MT1-MMP) on prostate cancer cell lines.

Authors:  O Nagakawa; K Murakami; T Yamaura; Y Fujiuchi; J Murata; H Fuse; I Saiki
Journal:  Cancer Lett       Date:  2000-07-31       Impact factor: 8.679

3.  Increased expression of membrane type 1-matrix metalloproteinase in head and neck carcinoma.

Authors:  T Yoshizaki; H Sato; Y Maruyama; S Murono; M Furukawa; C S Park; M Seiki
Journal:  Cancer       Date:  1997-01-01       Impact factor: 6.860

4.  Membrane type I-matrix metalloproteinase (MT1-MMP) is internalised by two different pathways and is recycled to the cell surface.

Authors:  Albert Remacle; Gillian Murphy; Christian Roghi
Journal:  J Cell Sci       Date:  2003-08-12       Impact factor: 5.285

5.  Mechanism of cell surface activation of 72-kDa type IV collagenase. Isolation of the activated form of the membrane metalloprotease.

Authors:  A Y Strongin; I Collier; G Bannikov; B L Marmer; G A Grant; G I Goldberg
Journal:  J Biol Chem       Date:  1995-03-10       Impact factor: 5.157

6.  A matrix metalloproteinase expressed on the surface of invasive tumour cells.

Authors:  H Sato; T Takino; Y Okada; J Cao; A Shinagawa; E Yamamoto; M Seiki
Journal:  Nature       Date:  1994-07-07       Impact factor: 49.962

Review 7.  The metzincins--topological and sequential relations between the astacins, adamalysins, serralysins, and matrixins (collagenases) define a superfamily of zinc-peptidases.

Authors:  W Stöcker; F Grams; U Baumann; P Reinemer; F X Gomis-Rüth; D B McKay; W Bode
Journal:  Protein Sci       Date:  1995-05       Impact factor: 6.725

8.  Matrix metalloproteinases regulate neovascularization by acting as pericellular fibrinolysins.

Authors:  N Hiraoka; E Allen; I J Apel; M R Gyetko; S J Weiss
Journal:  Cell       Date:  1998-10-30       Impact factor: 41.582

9.  Expression of matrix metalloproteinases during rat skin wound healing: evidence that membrane type-1 matrix metalloproteinase is a stromal activator of pro-gelatinase A.

Authors:  A Okada; C Tomasetto; Y Lutz; J P Bellocq; M C Rio; P Basset
Journal:  J Cell Biol       Date:  1997-04-07       Impact factor: 10.539

10.  Membrane-type 1 matrix metalloprotease (MT1-MMP) enables invasive migration of glioma cells in central nervous system white matter.

Authors:  A T Beliën; P A Paganetti; M E Schwab
Journal:  J Cell Biol       Date:  1999-01-25       Impact factor: 10.539

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