Evidence map›Paper›PMID 33154487›Full record

ArticleScientific reports2020

Tumor cell MT1-MMP is dispensable for osteosarcoma tumor growth, bone degradation and lung metastasis.

Signe Z Ingvarsen, Henrik Gårdsvoll, Sander van Putten, Kirstine S Nørregaard, Oliver Krigslund, Josephine A Meilstrup, Collin Tran, Henrik J Jürgensen, Maria C Melander, Carsten H Nielsen and 4 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

10 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Osteosarcoma and Metastasis.Frontiers in oncology · 2021
    Review
  10. Review
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

14 authors at 5 institutions in 2 countries.

Signe Z IngvarsenFinsen Laboratory, Rigshospitalet/Biotech Research and Innovation Center (BRIC), University of Copenhagen (UCPH), Ole Maaløes Vej 5, 2200, Copenhagen N, Denmark.
Henrik GårdsvollFinsen Laboratory, Rigshospitalet/Biotech Research and Innovation Center (BRIC), University of Copenhagen (UCPH), Ole Maaløes Vej 5, 2200, Copenhagen N, Denmark.
Sander van PuttenFinsen Laboratory, Rigshospitalet/Biotech Research and Innovation Center (BRIC), University of Copenhagen (UCPH), Ole Maaløes Vej 5, 2200, Copenhagen N, Denmark.
Kirstine S NørregaardFinsen Laboratory, Rigshospitalet/Biotech Research and Innovation Center (BRIC), University of Copenhagen (UCPH), Ole Maaløes Vej 5, 2200, Copenhagen N, Denmark.
Oliver KrigslundFinsen Laboratory, Rigshospitalet/Biotech Research and Innovation Center (BRIC), University of Copenhagen (UCPH), Ole Maaløes Vej 5, 2200, Copenhagen N, Denmark.
Josephine A MeilstrupBRIC, UCPH, Copenhagen, Denmark.
Collin TranProteases and Tissue Remodeling Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, USA.
Henrik J JürgensenFinsen Laboratory, Rigshospitalet/Biotech Research and Innovation Center (BRIC), University of Copenhagen (UCPH), Ole Maaløes Vej 5, 2200, Copenhagen N, Denmark.
Maria C MelanderIn Vivo Pharmacology, Symphogen A/S, Ballerup, Denmark.
Carsten H NielsenDepartment of Clinical Physiology, Nuclear Medicine & PET and Cluster for Molecular Imaging, Rigshospitalet and UCPH, Copenhagen, Denmark.
Andreas KjaerDepartment of Clinical Physiology, Nuclear Medicine & PET and Cluster for Molecular Imaging, Rigshospitalet and UCPH, Copenhagen, Denmark.
Thomas H BuggeProteases and Tissue Remodeling Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, USA.
Lars H EngelholmFinsen Laboratory, Rigshospitalet/Biotech Research and Innovation Center (BRIC), University of Copenhagen (UCPH), Ole Maaløes Vej 5, 2200, Copenhagen N, Denmark.
Niels BehrendtFinsen Laboratory, Rigshospitalet/Biotech Research and Innovation Center (BRIC), University of Copenhagen (UCPH), Ole Maaløes Vej 5, 2200, Copenhagen N, Denmark. niels.behrendt@finsenlab.dk.
Rigshospitalet · DKUniversity of Copenhagen · DKNational Institute of Dental and Craniofacial Research · USNational Institutes of Health · USSymphogen (Denmark) · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The membrane-anchored matrix metalloprotease MT1-MMP is a potent collagenolytic enzyme with a well-established role in extracellular matrix turnover and cellular invasion into collagen-rich tissues. MT1-MMP is highly expressed in various types of cancer and has been demonstrated to be directly involved in several stages of tumor progression, including primary tumor growth, angiogenesis, invasion and metastasis. Osteosarcoma is the most common type of primary bone cancer. This disease is characterized by invasive tumor growth, leading to extensive bone destruction, and metastasis to the lungs. The tumor cells in human osteosarcoma display a strong expression of MT1-MMP, but the role of MT1-MMP in osteosarcoma progression is currently unknown. In this study, we investigated the role of MT1-MMP during various stages of osteosarcoma development. We utilized an optimized orthotopic murine osteosarcoma model and human osteosarcoma cells in which the MT1-MMP gene was knocked out using CRISPR/Cas9. We observed a strong expression of MT1-MMP in wildtype cells of both primary tumors and lung metastases, but, surprisingly, MT1-MMP deficiency did not affect primary tumor growth, bone degradation or the formation and growth of lung metastases. We therefore propose that, unlike findings reported in other cancers, tumor-expressed MT1-MMP is dispensable for all stages of osteosarcoma progression.

Indexed as

AnimalsBone and BonesBone NeoplasmsCell Line, TumorCell ProliferationCRISPR-Cas SystemsDisease ProgressionGene Knockdown TechniquesHumansLung NeoplasmsMatrix Metalloproteinase 14MiceNeoplasm InvasivenessOsteosarcomaMatrix Metalloproteinase 14

Identifiers

PMID33154487
PMCPMC7645741
OpenAlexW3097551332

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.