Evidence map›Paper›PMID 35371977›Full record

ArticleFrontiers in oncology2022

The Metalloprotease-Disintegrin ADAM8 Alters the Tumor Suppressor miR-181a-5p Expression Profile in Glioblastoma Thereby Contributing to Its Aggressiveness.

Agnes Schäfer, Lara Evers, Lara Meier, Uwe Schlomann, Miriam H A Bopp, Gian-Luca Dreizner, Olivia Lassmann, Aaron Ben Bacha, Andreea-Cristina Benescu, Mirza Pojskic and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

15 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Review
  3. Expert opinion on therapeutic targets · 2024
    Review
  4. ADAM8 promotes alcoholic liver fibrosis through the MAPK signaling pathway.The journal of physiological sciences : JPS · 2024
    Article
  5. Review
  6. Article
  7. Article
  8. Article
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  11. Review
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  14. Article
  15. Associations ofInternational journal of molecular sciences · 2022
    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

15 authors at 1 institution in 1 country.

Agnes SchäferDepartment of Neurosurgery, Philipps University Marburg, Marburg, Germany.
Lara EversDepartment of Neurosurgery, Philipps University Marburg, Marburg, Germany.
Lara MeierDepartment of Neurosurgery, Philipps University Marburg, Marburg, Germany.
Uwe SchlomannDepartment of Neurosurgery, Philipps University Marburg, Marburg, Germany.
Miriam H A BoppDepartment of Neurosurgery, Philipps University Marburg, Marburg, Germany.
Gian-Luca DreiznerDepartment of Neurosurgery, Philipps University Marburg, Marburg, Germany.
Olivia LassmannDepartment of Neurosurgery, Philipps University Marburg, Marburg, Germany.
Aaron Ben BachaDepartment of Neurosurgery, Philipps University Marburg, Marburg, Germany.
Andreea-Cristina BenescuDepartment of Neurosurgery, Philipps University Marburg, Marburg, Germany.
Mirza PojskicDepartment of Neurosurgery, Philipps University Marburg, Marburg, Germany.
Christian PreußerCore Facility Extracellular Vesicles, Philipps University of Marburg - Medical Faculty, Marburg, Germany.
Elke Pogge von StrandmannCore Facility Extracellular Vesicles, Philipps University of Marburg - Medical Faculty, Marburg, Germany.
Barbara CarlDepartment of Neurosurgery, Philipps University Marburg, Marburg, Germany.
Christopher NimskyDepartment of Neurosurgery, Philipps University Marburg, Marburg, Germany.
Jörg W BartschDepartment of Neurosurgery, Philipps University Marburg, Marburg, Germany.
Philipps University of Marburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma (GBM) as the most common and aggressive brain tumor is characterized by genetic heterogeneity, invasiveness, radio-/chemoresistance, and occurrence of GBM stem-like cells. The metalloprotease-disintegrin ADAM8 is highly expressed in GBM tumor and immune cells and correlates with poor survival. In GBM, ADAM8 affects intracellular kinase signaling and increases expression levels of osteopontin/SPP1 and matrix metalloproteinase 9 (MMP9) by an unknown mechanism. Here we explored whether microRNA (miRNA) expression levels could be regulators of MMP9 expression in GBM cells expressing ADAM8. Initially, we identified several miRNAs as dysregulated in ADAM8-deficient U87 GBM cells. Among these, the tumor suppressor miR-181a-5p was significantly upregulated in ADAM8 knockout clones. By inhibiting kinase signaling, we found that ADAM8 downregulates expression of miR-181a-5p

Indexed as

ADAM8extracellular vesiclesglioblastomamiR-181a-5pmiRNAMMP9MR spectroscopytumor microenvironment

Identifiers

PMID35371977
PMCPMC8964949
OpenAlexW4220678486

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.