Evidence map›Paper›PMID 11828004›Full record

ArticleThe Journal of experimental medicine2002

Matrix metalloproteinases (MMPs) regulate fibrin-invasive activity via MT1-MMP-dependent and -independent processes.

Kevin B Hotary, Ikuo Yana, Farideh Sabeh, Xiao-Yan Li, Kenn Holmbeck, Henning Birkedal-Hansen, Edward D Allen, Nobuaki Hiraoka, Stephen J Weiss

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
8.2field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

77 citing papers in PubMed, 218 citations in OpenAlex.

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  12. Mechanoreciprocity in cell migration.Nature cell biology · 2018
    Review
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17 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 1 country.

Kevin B HotaryUniversity of Michigan Comprehensive Cancer Center, Ann Arbor, MI 48109, USA.
Ikuo Yana
Farideh Sabeh
Xiao-Yan Li
Kenn Holmbeck
Henning Birkedal-Hansen
Edward D Allen
Nobuaki Hiraoka
Stephen J Weiss
Michigan Cancer Research Consortium · USUniversity of Michigan–Ann Arbor · USNational Institute of Dental and Craniofacial Research · USMichigan Center for Translational Pathology · US

Funding

FUNCTION OF THE MEMBRANE TYPE MATRIX METALLOPROTEINASER01CA071699 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WEISS, STEPHEN J · 1997 to 2024
$7.3M
METALLOPROTEASE DEPENDENT FIBRINOLYSIS AND ANGIOGENESISR01CA088308 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WEISS, STEPHEN J · 2000 to 2015
$4.6M
Matrix Metalloproteinases: Remodelling of the ExtracelluZ01DE000676 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI ROBEY, PAMELA G · 1996 to 2008
$2.3M
NCI NIH HHS CA71699NCI NIH HHS CA88308NCI NIH HHS R01 CA071699NCI NIH HHS R01 CA088308
6 · The paper itself

Abstract

Cross-linked fibrin is deposited in tissues surrounding wounds, inflammatory sites, or tumors and serves not only as a supporting substratum for trafficking cells, but also as a structural barrier to invasion. While the plasminogen activator-plasminogen axis provides cells with a powerful fibrinolytic system, plasminogen-deleted animals use alternate proteolytic processes that allow fibrin invasion to proceed normally. Using fibroblasts recovered from wild-type or gene-deleted mice, invasion of three-dimensional fibrin gels proceeded in a matrix metalloproteinase (MMP)-dependent fashion. Consistent with earlier studies supporting a singular role for the membrane-anchored MMP, MT1-MMP, in fibrin-invasive events, fibroblasts from MT1-MMP-null mice displayed an early defect in invasion. However, MT1-MMP-deleted fibroblasts circumvented this early deficiency and exhibited compensatory fibrin-invasive activity. The MT1-MMP-independent process was sensitive to MMP inhibitors that target membrane-anchored MMPs, and further studies identified MT2-MMP and MT3-MMP, but not MT4-MMP, as alternate pro-invasive factors. Given the widespread distribution of MT1-, 2-, and 3-MMP in normal and neoplastic cells, these data identify a subset of membrane-anchored MMPs that operate in an autonomous fashion to drive fibrin-invasive activity.

Indexed as

AnimalsCell LineCHO CellsCricetinaeDogsFibrinFibrinolysisFibroblastsMatrix Metalloproteinase 14Matrix Metalloproteinase 15Matrix Metalloproteinase 16Matrix MetalloproteinasesMatrix Metalloproteinases, Membrane-AssociatedMetalloendopeptidasesMetallothionein 3MiceFibrinMatrix Metalloproteinase 14Matrix Metalloproteinase 15Matrix Metalloproteinase 16Matrix MetalloproteinasesMatrix Metalloproteinases, Membrane-AssociatedMetalloendopeptidasesMetallothionein 3Mmp14 protein, mouseMmp15 protein, mouseMmp16 protein, mouseMt3 protein, mouse

Identifiers

PMID11828004
PMCPMC2193588
OpenAlexW2106965899

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.