Evidence map›Paper›PMID 17237343›Full record

ReviewPhysiological reviews2007

Matrix metalloproteinases in lung: multiple, multifarious, and multifaceted.

Kendra J Greenlee, Zena Werb, Farrah Kheradmand

Open access · greenAbstract readReview
In one paragraph

Review in Physiological reviews, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 203 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
203citing papers in PubMed, 1 pooled it
12.0field-weighted citation impact, top 1% 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

203 citing papers in PubMed, 1 synthesis or guideline pooled it, 480 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Trial
  6. Trial
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Advances in Inhaled Nanoparticle Drug Delivery for Pulmonary Disease Management.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Review
  14. Article
  15. Review
  16. The AhR Is a Critical Regulator of the Pulmonary Response to Cannabis Smoke.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  17. Article
  18. Article
  19. Article
  20. Dipeptidyl peptidase-1 inhibitors in bronchiectasis.European respiratory review : an official journal of the European Respiratory Society · 2025
    Review

143 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

3 authors at 1 institution in 1 country.

Kendra J GreenleeDepartments of Medicine and Immunology, Baylor College of Medicine, Houston, Texas, USA.
Zena Werb
Farrah Kheradmand
Baylor College of Medicine · US

Funding

Sulfs and Injury Repair in Mucosal EpitheliaP01AI053194 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WERB, ZENA · 2002 to 2012
$13.4M
RESEARCH TRAINING IN LUNG DISEASET32HL007747 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI ROSAS, IVAN O. · 1993 to 2020
$5.1M
Immune Modulators of Inflammation in Severe COPDR01HL072419 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI KHERADMAND, FARRAH · 2002 to 2010
$1.9M
Smoke-induced AP-1 controls mucous vs squamous phenotypeR01HL075602 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WERB, ZENA · 2004 to 2007
$1.4M
The Role of Proteases in Lung Inflammation &RemodelingK02HL072062 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI KHERADMAND, FARRAH · 2003 to 2007
$498k
NHLBI NIH HHS K02 HL072062NHLBI NIH HHS K02-HL-72062NHLBI NIH HHS R01 HL072419NHLBI NIH HHS R01 HL075602NHLBI NIH HHS R01-HL-72419NHLBI NIH HHS R01-HL-75602NHLBI NIH HHS T32 HL007747NHLBI NIH HHS T32-HL-07747NIAID NIH HHS P01 AI053194NIAID NIH HHS P01-AI-53194
6 · The paper itself

Abstract

The matrix metalloproteinases (MMPs), a family of 25 secreted and cell surface-bound neutral proteinases, process a large array of extracellular and cell surface proteins under normal and pathological conditions. MMPs play critical roles in lung organogenesis, but their expression, for the most part, is downregulated after generation of the alveoli. Our knowledge about the resurgence of the MMPs that occurs in most inflammatory diseases of the lung is rapidly expanding. Although not all members of the MMP family are found within the lung tissue, many are upregulated during the acute and chronic phases of these diseases. Furthermore, potential MMP targets in the lung include all structural proteins in the extracellular matrix (ECM), cell adhesion molecules, growth factors, cytokines, and chemokines. However, what is less known is the role of MMP proteolysis in modulating the function of these substrates in vivo. Because of their multiplicity and substantial substrate overlap, MMPs are thought to have redundant functions. However, as we explore in this review, such redundancy most likely evolved as a necessary compensatory mechanism given the critical regulatory importance of MMPs. While inhibition of MMPs has been proposed as a therapeutic option in a variety of inflammatory lung conditions, a complete understanding of the biology of these complex enzymes is needed before we can reasonably consider them as therapeutic targets.

Indexed as

AnimalsHumansLungMatrix MetalloproteinasesMatrix Metalloproteinases

Identifiers

PMID17237343
PMCPMC2656382
OpenAlexW2162313829

What OpenQuestion holds

Textmetadata
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.