Evidence map›Paper›PMID 32872536›Full record

ArticleCancers2020

Neoplastic Cells are the Major Source of MT-MMPs in

Ina Thome, Raphael Lacle, Andreas Voß, Ginette Bortolussi, Georgios Pantazis, Ansgar Schmidt, Catharina Conrad, Ralf Jacob, Nina Timmesfeld, Jörg W Bartsch and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.6field-weighted citation impact, top 35% 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

11 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Astrocytoma with high-grade features and MYBL1-MMP16 fusion.Surgical neurology international · 2024
    Article
  6. Molecular Mechanisms Driven by MT4-MMP in Cancer Progression.International journal of molecular sciences · 2023
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. 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

11 authors at 2 institutions in 1 country.

Ina ThomeDepartments of Neuropathology, Philipps University Marburg, 35043 Marburg, Germany.
Raphael LacleDepartments of Neuropathology, Philipps University Marburg, 35043 Marburg, Germany.
Andreas VoßDepartments of Neuropathology, Philipps University Marburg, 35043 Marburg, Germany.
Ginette BortolussiDepartments of Neuropathology, Philipps University Marburg, 35043 Marburg, Germany.
Georgios PantazisDepartments of Neuropathology, Philipps University Marburg, 35043 Marburg, Germany.
Ansgar SchmidtDepartments of Pathology, Philipps University Marburg, 35043 Marburg, Germany.
Catharina ConradDepartments of Neuropathology, Philipps University Marburg, 35043 Marburg, Germany.
Ralf JacobDepartments of Clinical Cytobiology and Cytopathology, Philipps University Marburg, 35037 Marburg, Germany.
Nina TimmesfeldDepartment of Medical Informatics, Biometry and Epidemiology, Ruhr University Bochum, 44780 Bochum, Germany.
Jörg W BartschDepartments of Neurosurgery, Philipps University Marburg, 35043 Marburg, Germany.
Axel PagenstecherDepartments of Neuropathology, Philipps University Marburg, 35043 Marburg, Germany.
Philipps University of Marburg · DERuhr University Bochum · DE

Funding

Cancer Research UK C35513/A11931Wilhelm Sander-Stiftung 2002.090.1
6 · The paper itself

Abstract

Tumor-cell infiltration is a major obstacle to successful therapy for brain tumors. Membrane-type matrix metalloproteinases (MT-MMPs), a metzincin subfamily of six proteases, are important mediators of infiltration. The cellular source of MT-MMPs and their role in glioma biology, however, remain controversial. Thus, we comprehensively analyzed the expression of MT-MMPs in primary brain tumors. All MT-MMPs were differentially expressed in primary brain tumors. In diffuse gliomas, MT-MMP1, -3, and -4 were predominantly expressed by IDH1

Indexed as

gliomainvasionisocitrate dehydrogenasematrix metalloproteasesorganotypic cell invasion assay

Identifiers

PMID32872536
PMCPMC7565296
OpenAlexW3081810541

What OpenQuestion holds

Textmetadata
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.