Evidence map›Paper›PMID 36187350›Full record

ArticleFrontiers in molecular neuroscience2022

The impact of heme biosynthesis regulation on glioma aggressiveness: Correlations with diagnostic molecular markers.

Mario Mischkulnig, Barbara Kiesel, Thomas Rötzer-Pejrimovsky, Martin Borkovec, Alexandra Lang, Matthias Millesi, Lisa I Wadiura, Shawn Hervey-Jumper, Josef M Penninger, Mitchel S Berger and 2 more

Abstract read
In one paragraph

Article in Frontiers in molecular neuroscience, 2022. 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
–field-weighted citation impact
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.

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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

12 authors.

Mario MischkulnigDepartment of Neurosurgery, Medical University of Vienna, Vienna, Austria.
Barbara KieselDepartment of Neurosurgery, Medical University of Vienna, Vienna, Austria.
Thomas Rötzer-PejrimovskyCentral Nervous System Tumors Unit, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Martin BorkovecDepartment of Neurosurgery, Medical University of Vienna, Vienna, Austria.
Alexandra LangDepartment of Neurosurgery, Medical University of Vienna, Vienna, Austria.
Matthias MillesiDepartment of Neurosurgery, Medical University of Vienna, Vienna, Austria.
Lisa I WadiuraDepartment of Neurosurgery, Medical University of Vienna, Vienna, Austria.
Shawn Hervey-JumperDepartment of Neurological Surgery, University of California, San Francisco, San Francisco, CA, United States.
Josef M PenningerInstitute of Molecular Biotechnology of the Austrian Academy of Sciences, Vienna, Austria.
Mitchel S BergerDepartment of Neurological Surgery, University of California, San Francisco, San Francisco, CA, United States.
Georg WidhalmDepartment of Neurosurgery, Medical University of Vienna, Vienna, Austria.
Friedrich ErhartDepartment of Neurosurgery, Medical University of Vienna, Vienna, Austria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The prognosis of diffusely infiltrating glioma patients is dismal but varies greatly between individuals. While characterization of gliomas primarily relied on histopathological features, molecular markers increasingly gained importance and play a key role in the recently published 5 Materials and methods: In this study, patient data were derived from the "The Cancer Genome Atlas" (TCGA) lower-grade glioma and glioblastoma cohorts. We identified diffusely infiltrating gliomas correlating molecular tumor diagnosis according to the most recent WHO classification with heme biosynthesis mRNA expression. The following molecular markers were analyzed: EGFR amplification, TERT promoter mutation, CDKN2A/B homozygous loss, chromosome 7 + /10- aneuploidy, MGMT methylation, IDH mutation, ATRX loss, p53 mutation and 1p19q codeletion. Subsequently, we calculated the heme biosynthesis mRNA expression signature for correlation with distinct molecular glioma markers/molecular subgroups and performed survival analyses. Results: A total of 649 patients with available data on up-to-date molecular markers and heme biosynthesis mRNA expression were included. According to analysis of individual molecular markers, we found a significantly higher heme biosynthesis mRNA expression signature in gliomas with IDH wildtype ( Conclusion: Our data demonstrate a significant correlation between heme biosynthesis regulation and diagnostic molecular markers and a prognostic relevance independent of these established markers. Consequently, heme biosynthesis expression is a promising biomarker for glioma aggressiveness and might constitute a potential target for novel therapeutic approaches.

Indexed as

gliomaheme biosynthesismolecular markersmRNATCGA

Identifiers

PMID36187350
PMCPMC9515895

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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.