Evidence map›Paper›PMID 34053190›Full record

ArticleAnnals of clinical and translational neurology2021

Transcriptomic signature of painful human neurofibromatosis type 2 schwannomas.

Phanidhar Kukutla, Sherif G Ahmed, Daniel M DuBreuil, Ahmed Abdelnabi, Murat Cetinbas, Giulia Fulci, Berent Aldikacti, Anat Stemmer-Rachamimov, Scott R Plotkin, Brian Wainger and 2 more

Open access · goldAbstract read
In one paragraph

Article in Annals of clinical and translational neurology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 31% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. 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

12 authors at 4 institutions in 1 country.

Phanidhar KukutlaDepartment of Anesthesia, Critical Care, and Pain Medicine, Massachusetts General Hospital (MGH), Harvard Medical School (HMS), Boston, Massachusetts, 02114, USA.
Sherif G AhmedDepartment of Anesthesia, Critical Care, and Pain Medicine, Massachusetts General Hospital (MGH), Harvard Medical School (HMS), Boston, Massachusetts, 02114, USA.
Daniel M DuBreuilDepartment of Neurology, MGH, HMS, Boston, Massachusetts, USA.ORCID 0000-0001-6202-4049
Ahmed AbdelnabiDepartment of Anesthesia, Critical Care, and Pain Medicine, Massachusetts General Hospital (MGH), Harvard Medical School (HMS), Boston, Massachusetts, 02114, USA.ORCID 0000-0002-9782-5222
Murat CetinbasDepartment of Molecular Biology, MGH, Boston, Massachusetts, 02114, USA.
Giulia FulciDepartment of Anesthesia, Critical Care, and Pain Medicine, Massachusetts General Hospital (MGH), Harvard Medical School (HMS), Boston, Massachusetts, 02114, USA.
Berent AldikactiCenter for Engineering in Medicine, MGH, Boston, Massachusetts, 02114, USA.ORCID 0000-0002-8916-8007
Anat Stemmer-RachamimovDepartment of Molecular Biology, MGH, Boston, Massachusetts, 02114, USA.
Scott R PlotkinDepartment of Neurology, MGH, HMS, Boston, Massachusetts, USA.
Brian WaingerDepartment of Anesthesia, Critical Care, and Pain Medicine, Massachusetts General Hospital (MGH), Harvard Medical School (HMS), Boston, Massachusetts, 02114, USA.
Ruslan I SadreyevDepartment of Molecular Biology, MGH, Boston, Massachusetts, 02114, USA.
Gary J BrennerDepartment of Anesthesia, Critical Care, and Pain Medicine, Massachusetts General Hospital (MGH), Harvard Medical School (HMS), Boston, Massachusetts, 02114, USA.ORCID 0000-0002-4586-1723
Harvard University · USMGH Institute of Health Professions · USBroad Institute · USCenter for Systems Biology · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Schwannomas are benign neoplasms that can cause gain- and loss-of-function neurological phenotypes, including severe, intractable pain. To investigate the molecular mechanisms underlying schwannoma-associated pain we compared the RNA sequencing profile of painful and non-painful schwannomas from NF2 patients. Distinct segregation of painful and non-painful tumors by gene expression patterns was observed. Differential expression analysis showed the upregulation of fibroblast growth factor 7 (FGF7) in painful schwannomas. Behavioral support for this finding was observed using a xenograft human NF2-schwannoma model in nude mice. In this model, over-expression of FGF7 in intra-sciatically implanted NF2 tumor cells generated pain behavior compared with controls.

Indexed as

AnimalsCell Line, TumorFemaleFibroblast Growth Factor 7HumansMaleMiceMice, NudeNeurilemmomaNeurofibromatosis 2PainSciatic NeuropathySequence Analysis, RNATranscriptomeXenograft Model Antitumor AssaysFgf7 protein, mouseFibroblast Growth Factor 7

Identifiers

PMID34053190
PMCPMC8283170
OpenAlexW3164063106

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.