(Q36190097)

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Selective function-blocking monoclonal human antibody highlights the important role of membrane type-1 matrix metalloproteinase (MT1-MMP) in metastasis

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scholarly article

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Europe PubMed Central

12 August 2017

Selective function-blocking monoclonal human antibody highlights the important role of membrane type-1 matrix metalloproteinase (MT1-MMP) in metastasis (English)

1 reference

Europe PubMed Central

12 August 2017

5

object named as

Xin Ge

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Europe PubMed Central

12 August 2017

author name string

Albert G Remacle

1

1 reference

Europe PubMed Central

12 August 2017

Piotr Cieplak

2

1 reference

Europe PubMed Central

12 August 2017

Dong Hyun Nam

3

1 reference

Europe PubMed Central

12 August 2017

Sergey A Shiryaev

4

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Europe PubMed Central

12 August 2017

Alex Y Strongin

6

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Europe PubMed Central

12 August 2017

language of work or name

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publication date

7 November 2016

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Europe PubMed Central

12 August 2017

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Europe PubMed Central

12 August 2017

8

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Europe PubMed Central

12 August 2017

2781-2799

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Europe PubMed Central

12 August 2017

2

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Europe PubMed Central

12 August 2017

describes a project that uses

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Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC5356841/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

Development of a specific affinity-matured exosite inhibitor to MT1-MMP that efficiently inhibits tumor cell invasion in vitro and metastasis in vivo

1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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Matrix metalloproteinase-14 is a mechanically regulated activator of secreted MMPs and invasion.

1 reference

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ZDOCK server: interactive docking prediction of protein-protein complexes and symmetric multimers

1 reference

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A monoclonal antibody interferes with TIMP-2 binding and incapacitates the MMP-2-activating function of multifunctional, pro-tumorigenic MMP-14/MT1-MMP.

1 reference

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ModBase, a database of annotated comparative protein structure models and associated resources.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5356841

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1 reference

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1 reference

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Targeting a single function of the multifunctional matrix metalloprotease MT1-MMP: impact on lymphangiogenesis

1 reference

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CDR-H3 Diversity Is Not Required for Antigen Recognition by Synthetic Antibodies

1 reference

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Novel MT1-MMP small-molecule inhibitors based on insights into hemopexin domain function in tumor growth

1 reference

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1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5356841

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Intradomain cleavage of inhibitory prodomain is essential to protumorigenic function of membrane type-1 matrix metalloproteinase (MT1-MMP) in vivo.

1 reference

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Cancer cell-associated MT1-MMP promotes blood vessel invasion and distant metastasis in triple-negative mammary tumors

1 reference

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Dynamic interdomain interactions contribute to the inhibition of matrix metalloproteinases by tissue inhibitors of metalloproteinases.

1 reference

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New Strategies for the Next Generation of Matrix-Metalloproteinase Inhibitors: Selectively Targeting Membrane-Anchored MMPs with Therapeutic Antibodies

1 reference

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1 reference

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Biochemical characterization of the cellular glycosylphosphatidylinositol-linked membrane type-6 matrix metalloproteinase

1 reference

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The tissue inhibitors of metalloproteinases (TIMPs): an ancient family with structural and functional diversity

1 reference

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1 October 2017

Emerging concepts in the regulation of membrane-type 1 matrix metalloproteinase activity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5356841

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Proteolytic and non-proteolytic roles of membrane type-1 matrix metalloproteinase in malignancy

1 reference

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Matrix metalloproteinase proteolysis of the myelin basic protein isoforms is a source of immunogenic peptides in autoimmune multiple sclerosis

1 reference

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Selective inhibition of matrix metalloproteinase-14 blocks tumor growth, invasion, and angiogenesis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5356841

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Proteolytic interstitial cell migration: a five-step process.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5356841

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Mapping proteolytic cancer cell-extracellular matrix interfaces

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5356841

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The regulation of matrix metalloproteinases and their inhibitors.

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Mechanisms to inhibit matrix metalloproteinase activity: where are we in the development of clinically relevant inhibitors?

1 reference

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The other side of MMPs: protective roles in tumor progression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5356841

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Membrane type 1-matrix metalloproteinase: substrate diversity in pericellular proteolysis

1 reference

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MMPs as therapeutic targets--still a viable option?

1 reference

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Multi-step pericellular proteolysis controls the transition from individual to collective cancer cell invasion

1 reference

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Prostate cancer-associated membrane type 1-matrix metalloproteinase: a pivotal role in bone response and intraosseous tumor growth.

1 reference

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Membrane type-1 matrix metalloproteinase confers aneuploidy and tumorigenicity on mammary epithelial cells

1 reference

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Mislocalization and unconventional functions of cellular MMPs in cancer.

1 reference

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Furin regulates the intracellular activation and the uptake rate of cell surface-associated MT1-MMP.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5356841

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1 reference

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1 reference

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1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5356841

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1 reference

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1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5356841

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1 reference

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Membrane-type 1 matrix metalloproteinase enhances lymph node metastasis of gastric cancer

1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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A murine model of experimental metastasis to bone and bone marrow.

1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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2 July 2018

Crystal structure of the complex formed by the membrane type 1-matrix metalloproteinase with the tissue inhibitor of metalloproteinases-2, the soluble progelatinase A receptor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5356841

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Potent enzyme inhibitors derived from dromedary heavy-chain antibodies

1 reference

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Kinetics and physiologic relevance of the inactivation of alpha 1-proteinase inhibitor, alpha 1-antichymotrypsin, and antithrombin III by matrix metalloproteinases-1 (tissue collagenase), -2 (72-kDa gelatinase/type IV collagenase), and -3 (stromelys

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5356841

2 July 2018

Direct production of functional matrix metalloproteinase--14 without refolding or activation and its application for in vitro inhibition assays.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5356841

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Crystal structure of the catalytic domain of matrix metalloproteinase-1 in complex with the inhibitory domain of tissue inhibitor of metalloproteinase-1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5356841

22 September 2018

Interference with the complement system by tumor cell membrane type-1 matrix metalloproteinase plays a significant role in promoting metastasis in mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5356841

22 September 2018

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1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5356841

22 September 2018

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1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5356841

22 September 2018

A unique substrate binding mode discriminates membrane type-1 matrix metalloproteinase from other matrix metalloproteinases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5356841

22 September 2018

Mutation analysis of membrane type-1 matrix metalloproteinase (MT1-MMP). The role of the cytoplasmic tail Cys(574), the active site Glu(240), and furin cleavage motifs in oligomerization, processing, and self-proteolysis of MT1-MMP expressed in brea

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5356841

22 September 2018

The serpin alpha1-proteinase inhibitor is a critical substrate for gelatinase B/MMP-9 in vivo.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5356841

22 September 2018

A large-scale study of MT1-MMP as a marker for isolated tumor cells in peripheral blood and bone marrow in gastric cancer cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/27835863

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Matrilysin is much more efficient than other matrix metalloproteinases in the proteolytic inactivation of alpha 1-antitrypsin

1 reference

https://pubmed.ncbi.nlm.nih.gov/27835863

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MT1-MMP-deficient mice develop dwarfism, osteopenia, arthritis, and connective tissue disease due to inadequate collagen turnover

1 reference

https://pubmed.ncbi.nlm.nih.gov/27835863

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.18632/ONCOTARGET.13157

1 reference

Europe PubMed Central

12 August 2017

1 reference

Europe PubMed Central

12 August 2017

1 reference

Europe PubMed Central

12 August 2017

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