Evidence map›Paper›PMID 42507076›Full record

ArticleMolecular biology reports2026

Transcriptome-wide profiling of cystic and solid vestibular schwannomas reveals candidate long non-coding RNA signatures.

Nele Teichmann, Santhilal Subhash, Mario Giordano, Ashraqat Ahmed, Robert Geffers, Madjid Samii, Chandrasekhar Kanduri, Amir Samii, Souvik Kar

Erratum issuedAbstract read
In one paragraph

Article in Molecular biology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Nele TeichmannInternational Neuroscience Institute, Rudolf-Pichlmayr-Strasse 4, D-30625, Hannover, Germany.
Santhilal SubhashDepartment of Biosciences and Bioengineering, Indian Institute of Technology Jammu, Jammu, Jammu, Kashmir, India.
Mario GiordanoInternational Neuroscience Institute, Rudolf-Pichlmayr-Strasse 4, D-30625, Hannover, Germany.
Ashraqat AhmedInternational Neuroscience Institute, Rudolf-Pichlmayr-Strasse 4, D-30625, Hannover, Germany.
Robert GeffersGenome Analytics Research Group, Helmholtz Centre for Infection Research, Braunschweig, Germany.
Madjid SamiiInternational Neuroscience Institute, Rudolf-Pichlmayr-Strasse 4, D-30625, Hannover, Germany.
Chandrasekhar KanduriDepartment of Medical Biochemistry and Cell Biology, Institute of Biomedicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Amir SamiiInternational Neuroscience Institute, Rudolf-Pichlmayr-Strasse 4, D-30625, Hannover, Germany.
Souvik KarInternational Neuroscience Institute, Rudolf-Pichlmayr-Strasse 4, D-30625, Hannover, Germany. kar@ini-hannover.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vestibular schwannoma (VS) is a benign tumor growing from Schwann cells of the vestibulocochlear nerve (cranial nerve VIII), accounting for 6-8% of brain tumors. Cystic vestibular schwannoma (cVS) represents 10% of VS cases and is characterized by unpredictable growth and worse surgical outcomes compared to solid VS (sVS). The molecular mechanisms underlying this aggressive phenotype remain poorly understood. In this context, long non-coding RNAs (lncRNAs) are gaining increased interest as biomarkers for early diagnosis and improved clinical management. lncRNAs are RNA molecules that are longer than 200 nucleotides. They are known to regulate gene transcription and participate in chromatin remodeling through various mechanisms. However, their role in cVS is largely unexplored. In this study, we identified cVS-associated lncRNAs using patient-derived samples. Whole transcriptome analysis via RNA sequencing revealed 65 differentially expressed lncRNAs and 308 protein-coding genes (PCGs) between cVS and sVS. From these, we selected the top eight lncRNAs (TENM3-AS1, ADIRF-AS1, PCA3, RP11-108K14.12, RP11-728F11.4, AC132217.4, RP11-43F13.3, and EGFLAM-AS1), each showing significant correlation with more than 20 differentially expressed PCGs. The upregulation of PCA3 and ADIRF-AS1, and the downregulation of EGFLAM-AS1 in cVS, were further validated using qRT-PCR. Here, by transcriptome-wide approach, we demonstrate that lncRNAs are prevalent in cVS disease and are likely to play critical roles in regulating important signaling pathways involved in disease pathogenesis. We believe, that detailed future investigations on this set of identified lncRNAs can provide useful insights into the biology and, ultimately, contribute to biomarker development for this neoplasm.

Indexed as

Neuroma, AcousticRNA, Long NoncodingBiomarkers, TumorGene Expression ProfilingGene Expression Regulation, NeoplasticHumansSequence Analysis, RNATranscriptomeBiomarkers, TumorRNA, Long NoncodingBiomarker developmentCystic vestibular schwannomaDifferential gene expressionLong non-coding RNAsRNA sequencingVestibular schwannoma

Identifiers

PMID42507076
PMCPMC13407589

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.