Evidence map›Paper›PMID 29761368›Full record

ArticleJournal of neuro-oncology2018

IDH1 mutation in human glioma induces chemical alterations that are amenable to optical Raman spectroscopy.

Ortrud Uckermann, Wenmin Yao, Tareq A Juratli, Roberta Galli, Elke Leipnitz, Matthias Meinhardt, Edmund Koch, Gabriele Schackert, Gerald Steiner, Matthias Kirsch

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In one paragraph

Article in Journal of neuro-oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
4.6field-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

26 citing papers in PubMed, 51 citations in OpenAlex.

  1. Trial
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  4. Towards Optical Biopsy in Glioma Surgery.International journal of molecular sciences · 2025
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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

10 authors at 3 institutions in 1 country.

Ortrud UckermannNeurosurgery, University Hospital Carl Gustav Carus, TU Dresden, Fetscherstr. 74, 01307, Dresden, Germany.ORCID http://orcid.org/0000-0001-8196-604X
Wenmin YaoNeurosurgery, University Hospital Carl Gustav Carus, TU Dresden, Fetscherstr. 74, 01307, Dresden, Germany.
Tareq A JuratliNeurosurgery, University Hospital Carl Gustav Carus, TU Dresden, Fetscherstr. 74, 01307, Dresden, Germany.
Roberta GalliDepartment of Anesthesiology and Intensive Care Medicine, Faculty of Medicine, Clinical Sensoring and Monitoring, TU Dresden, Fetscherstr. 74, 01307, Dresden, Germany.
Elke LeipnitzNeurosurgery, University Hospital Carl Gustav Carus, TU Dresden, Fetscherstr. 74, 01307, Dresden, Germany.
Matthias MeinhardtNeuropathology, University Hospital Carl Gustav Carus, TU Dresden, Dresden, Germany.
Edmund KochDepartment of Anesthesiology and Intensive Care Medicine, Faculty of Medicine, Clinical Sensoring and Monitoring, TU Dresden, Fetscherstr. 74, 01307, Dresden, Germany.
Gabriele SchackertNeurosurgery, University Hospital Carl Gustav Carus, TU Dresden, Fetscherstr. 74, 01307, Dresden, Germany.
Gerald SteinerDepartment of Anesthesiology and Intensive Care Medicine, Faculty of Medicine, Clinical Sensoring and Monitoring, TU Dresden, Fetscherstr. 74, 01307, Dresden, Germany. Gerald.steiner@tu-dresden.de.
Matthias KirschNeurosurgery, University Hospital Carl Gustav Carus, TU Dresden, Fetscherstr. 74, 01307, Dresden, Germany. Matthias.kirsch@uniklinikum-dresden.de.
University Hospital Carl Gustav Carus · DETechnische Universität Dresden · DEGerman Cancer Research Center · DE

Funding

Bundesministerium für Bildung und Forschung 13N13807
6 · The paper itself

Abstract

introductionMutations in the isocytrate dehydrogenase 1 (IDH1) gene are early genetic events in glioma pathogenesis and cause profound metabolic changes. Because this genotype is found in virtually every tumor cell, therapies targeting mutant IDH1 protein are being developed. The intraoperative administration of those therapies would require fast technologies for the determination of IDH1 genotype. As of today, there is no such diagnostic test available. Recently, infrared spectroscopy was shown to bridge this gap. Here, we tested Raman spectroscopy for analysis of IDH1 genotype in glioma, which constitutes an alternative contact-free technique with the potential of being applicable in situ.

methodsHuman glioma samples (n = 36) were obtained during surgery and cryosections were prepared. IDH1 mutations were assessed using DNA sequencing and 100 Raman spectra were obtained for each sample.

resultsAnalysis of Raman spectra revealed increased intensities in spectral bands related to DNA in IDH1 mutant glioma while bands assigned to molecular vibrations of lipids were significantly decreased. Moreover, intensities of Raman bands assigned to proteins differed in IDH1 mutant and IDH1 wild-type glioma, suggesting alterations in the protein profile. The selection of five bands (498, 826, 1003, 1174 and 1337 cm

conclusionRaman spectroscopy constitutes a simple, rapid and safe procedure for determination of the IDH1 mutation that shows great promise for clinically relevant in situ diagnostics.

Indexed as

MutationBrain NeoplasmsGliomaHumansIsocitrate DehydrogenasePrognosisSpectrum Analysis, RamanIDH1 protein, humanIsocitrate DehydrogenaseBrain tumorIntraoperativePersonalized medicineVibrational spectroscopy

Identifiers

PMID29761368
OpenAlexW2804674191

What OpenQuestion holds

Textmetadata
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.