Evidence map›Paper›PMID 37217626›Full record

ArticleEuropean journal of human genetics : EJHG2023

New insights into the molecular basis of spinal neurofibromatosis type 1.

Paola Bettinaglio, Eleonora Mangano, Viviana Tritto, Roberta Bordoni, Rosina Paterra, Arianna Borghi, Marinella Volontè, Cristina Battaglia, Veronica Saletti, Claudia Cesaretti and 4 more

Open access · greenAbstract read
In one paragraph

Article in European journal of human genetics : EJHG, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.4field-weighted citation impact, top 36% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. 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

14 authors at 5 institutions in 2 countries.

Paola Bettinaglio *Department of Medical Biotechnology and Translational Medicine (BIOMETRA), University of Milan, 20054, Segrate, Milan, Italy.
Eleonora Mangano *Institute of Biomedical Technologies (ITB) National Research Center (CNR), ITB-CNR, 20054, Segrate, Milan, Italy.
Viviana TrittoDepartment of Medical Biotechnology and Translational Medicine (BIOMETRA), University of Milan, 20054, Segrate, Milan, Italy.ORCID 0000-0002-4558-8376
Roberta BordoniInstitute of Biomedical Technologies (ITB) National Research Center (CNR), ITB-CNR, 20054, Segrate, Milan, Italy.
Rosina PaterraMolecular Neuro-Oncology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133, Milan, Italy.
Arianna BorghiMolecular Neuro-Oncology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133, Milan, Italy.ORCID 0000-0002-5529-9762
Marinella VolontèDepartment of Medical Biotechnology and Translational Medicine (BIOMETRA), University of Milan, 20054, Segrate, Milan, Italy.
Cristina BattagliaDepartment of Medical Biotechnology and Translational Medicine (BIOMETRA), University of Milan, 20054, Segrate, Milan, Italy.
Veronica SalettiDevelopmental Neurology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Mariani Foundation Center for Complex Disabilities, 20054, Milan, Italy.
Claudia CesarettiMedical Genetics Unit, Woman-Child-Newborn Department, Fondazione IRCCS Ca' Granda-Ospedale Maggiore Policlinico, 20122, Milan, Italy.
Federica NatacciMedical Genetics Unit, Woman-Child-Newborn Department, Fondazione IRCCS Ca' Granda-Ospedale Maggiore Policlinico, 20122, Milan, Italy.
Mariarosa A B MeloneDepartment of Advanced Medical and Surgical Sciences, 2nd Division of Neurology, Center for Rare Diseases and InterUniversity Center for Research in Neurosciences, University of Campania Luigi Vanvitelli, 80131, Naples, Italy.ORCID 0000-0002-7213-9277
Marica EoliMolecular Neuro-Oncology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133, Milan, Italy. marica.eoli@istituto-besta.it.
Paola RivaDepartment of Medical Biotechnology and Translational Medicine (BIOMETRA), University of Milan, 20054, Segrate, Milan, Italy. paola.riva@unimi.it.ORCID 0000-0001-6481-8467
University of Milan · ITFondazione IRCCS Istituto Neurologico Carlo Besta · ITFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico · ITInstitute of Biomedical Technologies · ITUniversity of Campania "Luigi Vanvitelli" · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spinal neurofibromatosis (SNF) is a form of neurofibromatosis type 1 (NF1) characterized by bilateral neurofibromas involving all spinal roots. The pathogenic mechanisms determining the SNF form are currently unknown. To verify the presence of genetic variants possibly related to SNF or classic NF1, we studied 106 sporadic NF1 and 75 SNF patients using an NGS panel of 286 genes encoding RAS pathway effectors and neurofibromin interactors and evaluated the expression of syndecans (SDC1, SDC2, SDC3, SDC4), the NF1 3' tertile interactors, by quantitative real-time PCR. We previously identified 75 and 106 NF1 variants in SNF and NF1 cohorts, respectively. The analysis of the distribution of pathogenic NF1 variants in the three NF1 tertiles showed a significantly higher prevalence of NF1 3' tertile mutations in SNF than in the NF1 cohort. We hypothesized a potential pathogenic significance of the 3' tertile NF1 variants in SNF. The analysis of syndecan expression on PBMCs RNAs from 16 SNF, 16 classic NF1 patients and 16 healthy controls showed that the expression levels of SDC2 and SDC3 were higher in SNF and NF1 patients than in controls; moreover, SDC2, SDC3 and SDC4 were significantly over expressed in patients mutated in the 3' tertile compared to controls. Two different mutational NF1 spectra seem to characterize SNF and classic NF1, suggesting a pathogenic role of NF1 3' tertile and its interactors, syndecans, in SNF. Our study, providing new insights on a possible role of neurofibromin C-terminal in SNF, could address effective personalized patient management and treatments.

Indexed as

NeurofibromatosesNeurofibromatosis 1Genes, Neurofibromatosis 1HumansMutationNeurofibromin 1SyndecansNeurofibromin 1Syndecans

Identifiers

PMID37217626
PMCPMC10400572
OpenAlexW4377242147

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.