Evidence map›Paper›PMID 26926389›Full record

ArticleNature communications2016

MT1-MMP sheds LYVE-1 on lymphatic endothelial cells and suppresses VEGF-C production to inhibit lymphangiogenesis.

Hoi Leong Xavier Wong, Guoxiang Jin, Renhai Cao, Shuo Zhang, Yihai Cao, Zhongjun Zhou

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

57 citing papers in PubMed, 81 citations in OpenAlex.

  1. Review
  2. Article
  3. Matrix Metalloproteinase 14 in Corneal Neovascularization.International journal of molecular sciences · 2026
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  9. Hyaluronan: An Architect and Integrator for Cancer and Neural Diseases.International journal of molecular sciences · 2025
    Review
  10. Article
  11. Review
  12. Review
  13. Lymphatic Vessels in Chronic Rhinosinusitis.Journal of inflammation research · 2024
    Article
  14. Article
  15. Article
  16. Angiogenesis-An Emerging Role in Organ Fibrosis.International journal of molecular sciences · 2023
    Review
  17. Article
  18. Review
  19. Review
  20. Article
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

6 authors at 3 institutions in 3 countries.

Hoi Leong Xavier WongShenzhen Institute of Research and Innovation, University of Hong Kong, Shenzhen 518057, China.
Guoxiang JinLi Ka Shing Faculty of Medicine, School of Biomedical Sciences, University of Hong Kong, 21 Sassoon Road, Hong Kong, China.
Renhai CaoDepartment of Microbiology and Tumor Center, Karolinska Institute, Stockholm 171 77, Sweden.
Shuo ZhangShenzhen Institute of Research and Innovation, University of Hong Kong, Shenzhen 518057, China.
Yihai CaoDepartment of Microbiology and Tumor Center, Karolinska Institute, Stockholm 171 77, Sweden.
Zhongjun ZhouShenzhen Institute of Research and Innovation, University of Hong Kong, Shenzhen 518057, China.
University of Hong Kong · HKKarolinska Institutet · SECity University of Hong Kong, Shenzhen Research Institute · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lymphangiogensis is involved in various pathological conditions, such as arthritis and cancer metastasis. Although many factors have been identified to stimulate lymphatic vessel growth, little is known about lymphangiogenesis inhibitors. Here we report that membrane type 1-matrix metalloproteinase (MT1-MMP) is an endogenous suppressor of lymphatic vessel growth. MT1-MMP-deficient mice exhibit spontaneous corneal lymphangiogenesis without concomitant changes in angiogenesis. Mice lacking MT1-MMP in either lymphatic endothelial cells or macrophages recapitulate corneal lymphangiogenic phenotypes observed in Mmp14(-/-) mice, suggesting that the spontaneous lymphangiogenesis is both lymphatic endothelial cells autonomous and macrophage associated. Mechanistically, MT1-MMP directly cleaves LYVE-1 on lymphatic endothelial cells to inhibit LYVE-1-mediated lymphangiogenic responses. In addition, MT1-MMP-mediated PI3Kδ signalling restrains the production of VEGF-C from prolymphangiogenic macrophages through repressing the activation of NF-κB signalling. Thus, we identify MT1-MMP as an endogenous inhibitor of physiological lymphangiogenesis.

Indexed as

AnimalsBone TransplantationCells, CulturedCorneaEndothelial CellsGene Expression RegulationGlycoproteinsLymphangiogenesisMacrophagesMatrix Metalloproteinase 14Membrane Transport ProteinsMiceMice, KnockoutVascular Endothelial Growth Factor CGlycoproteinsLYVE1 protein, mouseMatrix Metalloproteinase 14Membrane Transport ProteinsMmp14 protein, mouseVascular Endothelial Growth Factor Cvascular endothelial growth factor C, mouse

Identifiers

PMID26926389
PMCPMC4773521
OpenAlexW2292789581

What OpenQuestion holds

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LicenceCC BY
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.