Evidence map›Paper›PMID 30127875›Full record

ArticleOncology letters2018

Overexpression of macrophage migration inhibitory factor and functionally-related genes, D-DT, CD74, CD44, CXCR2 and CXCR4, in glioblastoma.

Mario Presti, Emanuela Mazzon, Maria Sofia Basile, Maria Cristina Petralia, Alessia Bramanti, Giuseppe Colletti, Placido Bramanti, Ferdinando Nicoletti, Paolo Fagone

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed, 2 pooled it
4.5field-weighted citation impact, top 5% 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

55 citing papers in PubMed, 2 syntheses or guidelines pooled it, 67 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Bioinformatics and biology insights · 2026
    Article
  6. Article
  7. Article
  8. Single-Cell RNA Sequencing of Ewing Sarcoma Tumors Demonstrates Transcriptional Heterogeneity and Clonal Evolution.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. AnPeerJ · 2023
    Article
  17. Article
  18. Article
  19. Article
  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

9 authors at 2 institutions in 1 country.

Mario PrestiDepartment of Biomedical and Biotechnological Sciences, Biological Tower, University of Catania, Catania I-95123, Italy.
Emanuela MazzonIRCCS Centro Neurolesi 'Bonino-Pulejo', Messina I-98124, Italy.
Maria Sofia BasileDepartment of Biomedical and Biotechnological Sciences, Biological Tower, University of Catania, Catania I-95123, Italy.
Maria Cristina PetraliaDepartment of Biomedical and Biotechnological Sciences, Biological Tower, University of Catania, Catania I-95123, Italy.
Alessia BramantiIRCCS Centro Neurolesi 'Bonino-Pulejo', Messina I-98124, Italy.
Giuseppe CollettiDepartment of Biomedical and Biotechnological Sciences, Biological Tower, University of Catania, Catania I-95123, Italy.
Placido BramantiIRCCS Centro Neurolesi 'Bonino-Pulejo', Messina I-98124, Italy.
Ferdinando NicolettiDepartment of Biomedical and Biotechnological Sciences, Biological Tower, University of Catania, Catania I-95123, Italy.
Paolo FagoneDepartment of Biomedical and Biotechnological Sciences, Biological Tower, University of Catania, Catania I-95123, Italy.
University of Catania · ITCentro Neurolesi Bonino Pulejo · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The macrophage migration inhibition factor (MIF) is a cytokine with multiple biological functions, including the cancer-associated processes, cell cycle deregulation, angiogenesis and metastatization. The present study investigated the expression of MIF and its functionally associated genes (D-DT, CD74, CD44, CXCR2 and CXCR4) in glioblastoma multiforme (GBM). The data were obtained from The Cancer Genome Atlas databank, through the cBioportal web-based utility (cbioportal.org/). A significant increase was observed in the majority of these genes in GBM samples compared with lower grade gliomas, however no significant correlation among the selected genes and the overall survival of the patients was identified. In contrast, the expression of MIF exhibited a trend toward an increase in overall survival and a significant increase of MIF expression was observed in samples of patients who underwent neoadjuvant treatment. In conclusion these data indicate that MIF and its receptors are involved in GBM progression and maintenance. Deciphering the precise biological significance in GBM would favor the adoption of tailored approaches to modulate the function of MIF and its associated genes for the treatment of the disease.

Indexed as

cluster of differentiation 74D-dopachrome tautomeraseglioblastomagliomamacrophage migration inhibitory factor

Identifiers

PMID30127875
PMCPMC6096183
OpenAlexW2809200263

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.