Evidence map›Paper›PMID 38672281›Full record

ArticleBiomedicines2024

The Roles of AGTRAP, ALKBH3, DIVERSIN, NEDD8 and RRM1 in Glioblastoma Pathophysiology and Prognosis.

Claudia Alexandra Dumitru, Nikolas Walter, Carl Ludwig Raven Siebert, Frederik Till Alexander Schäfer, Ali Rashidi, Belal Neyazi, Klaus-Peter Stein, Christian Mawrin, Ibrahim Erol Sandalcioglu

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Article
  3. 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 1 institution in 1 country.

Claudia Alexandra DumitruDepartment of Neurosurgery, Otto-von-Guericke University, 39120 Magdeburg, Germany.ORCID 0000-0003-2075-9164
Nikolas WalterDepartment of Neurosurgery, Otto-von-Guericke University, 39120 Magdeburg, Germany.
Carl Ludwig Raven SiebertDepartment of Neurosurgery, Otto-von-Guericke University, 39120 Magdeburg, Germany.
Frederik Till Alexander SchäferDepartment of Neurosurgery, Otto-von-Guericke University, 39120 Magdeburg, Germany.
Ali RashidiDepartment of Neurosurgery, Otto-von-Guericke University, 39120 Magdeburg, Germany.
Belal NeyaziDepartment of Neurosurgery, Otto-von-Guericke University, 39120 Magdeburg, Germany.
Klaus-Peter SteinDepartment of Neurosurgery, Otto-von-Guericke University, 39120 Magdeburg, Germany.
Christian MawrinDepartment of Neuropathology, Otto-von-Guericke University, 39120 Magdeburg, Germany.
Ibrahim Erol SandalciogluDepartment of Neurosurgery, Otto-von-Guericke University, 39120 Magdeburg, Germany.
Otto-von-Guericke-Universität Magdeburg · DE

Funding

Hartmann Stiftung N/A
6 · The paper itself

Abstract

This study determined the expression of five novel biomarker candidates in IDH wild-type glioblastoma (GBM) tissues compared to non-malign brain parenchyma, as well as their prognostic relevance for the GBM patients' outcomes. The markers were analysed by immunohistochemistry in tumour tissues (n = 186) and healthy brain tissues (n = 54). The association with the patients' overall survival (OS) and progression-free survival (PFS) was assessed by Kaplan-Meier and log-rank test. The prognostic value of the markers was determined using multivariate Cox proportional hazard models. AGTRAP, DIVERSIN, cytoplasmic NEDD8 (NEDD8c) and RRM1 were significantly overexpressed in tumour tissues compared to the healthy brain, while the opposite was observed for ALKBH3. AGTRAP, ALKBH3, NEDD8c and RRM1 were significantly associated with OS in univariate analysis. AGTRAP and RRM1 were also independent prognostic factors for OS in multivariate analysis. For PFS, only AGTRAP and NEDD8c reached significance in univariate analysis. Additionally, AGTRAP was an independent prognostic factor for PFS in multivariate models. Finally, combined analysis of the markers enhanced their prognostic accuracy. The combination AGTRAP/ALKBH3 had the strongest prognostic value for the OS of GBM patients. These findings contribute to a better understanding of the GBM pathophysiology and may help identify novel therapeutic targets in this type of cancer.

Indexed as

biomarkersIDH wild-type glioblastomamarker combinationsoverall survivalprognostic accuracyprogression-free survival

Identifiers

PMID38672281
PMCPMC11048029
OpenAlexW4395012407

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.