Evidence map›Paper›PMID 29262839›Full record

ArticleOrphanet journal of rare diseases2017

Receptor of ghrelin is expressed in cutaneous neurofibromas of individuals with neurofibromatosis 1.

Rafaela E Rozza-de-Menezes, Nicolle C Gaglionone, Raquel M Andrade-Losso, Orlando H K Siqueira, Lilian M Almeida, Kamila da S Peruzini, Marco A C Guimarães-Filho, Carolina I Brum, Mauro Geller, Karin S Cunha

Open access · goldAbstract readLetter
In one paragraph

Article in Orphanet journal of rare diseases, 2017. 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
1.1field-weighted citation impact, top 22% 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, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
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.

Rafaela E Rozza-de-MenezesGraduate Program in Pathology, School of Medicine, Hospital Universitário Antônio Pedro, Universidade Federal Fluminense, Av. Marquês do Paraná, 303, 4o andar, sala 01 - Centro, Niterói, RJ, 24033-900, Brazil.
Nicolle C GagliononeGraduate Program in Pathology, School of Medicine, Hospital Universitário Antônio Pedro, Universidade Federal Fluminense, Av. Marquês do Paraná, 303, 4o andar, sala 01 - Centro, Niterói, RJ, 24033-900, Brazil.
Raquel M Andrade-LossoGraduate Program in Pathology, School of Medicine, Hospital Universitário Antônio Pedro, Universidade Federal Fluminense, Av. Marquês do Paraná, 303, 4o andar, sala 01 - Centro, Niterói, RJ, 24033-900, Brazil.
Orlando H K SiqueiraDepartment of General and Specialized Surgery, School of Medicine, Universidade Federal Fluminense, Niterói, RJ, Brazil.
Lilian M AlmeidaGraduate Program in Pathology, School of Medicine, Hospital Universitário Antônio Pedro, Universidade Federal Fluminense, Av. Marquês do Paraná, 303, 4o andar, sala 01 - Centro, Niterói, RJ, 24033-900, Brazil.
Kamila da S PeruziniSchool of Medicine, Universidade Federal Fluminense, Niterói, RJ, Brazil.
Marco A C Guimarães-FilhoDepartment of General and Specialized Surgery, School of Medicine, Universidade Federal Fluminense, Niterói, RJ, Brazil.
Carolina I BrumDepartment of Pathology, School of Medicine, Universidade Federal Fluminense, Niterói, RJ, Brazil.
Mauro GellerDepartment of Immunology and Microbiology, School of Medicine, Centro Universitário Serra dos Órgãos (UNIFESO), Teresópolis, RJ, Brazil.
Karin S CunhaGraduate Program in Pathology, School of Medicine, Hospital Universitário Antônio Pedro, Universidade Federal Fluminense, Av. Marquês do Paraná, 303, 4o andar, sala 01 - Centro, Niterói, RJ, 24033-900, Brazil. karingcunha@gmail.com.
Universidade Federal Fluminense · BRHospital Universitário Antônio Pedro · BRUniversidade Federal do Rio de Janeiro · BR

Funding

FAPERJ (Fundação de Amparo à Pesquisa do Estado do Rio de Janeiro) E-26/110/409/2011
6 · The paper itself

Abstract

backgroundMultiple cutaneous neurofibromas are a hallmark of neurofibromatosis 1 (NF1). They begin to appear during puberty and increase in number and volume during pregnancy, suggesting a hormonal influence. Ghrelin is a hormone that acts via growth hormone secretagogue receptor (GHS-R), which is overexpressed in many neoplasms and is involved in tumorigenesis. We aimed to investigate GHS-R expression in NF1 cutaneous neurofibromas and its relationship with tumors volume, and patient's age and gender.

resultsSample comprised 108 cutaneous neurofibromas (55 large and 53 small tumors) from 55 NF1 individuals. GHS-R expression was investigated by immunohistochemistry in tissue micro and macroarrays and quantified using a digital computer-assisted method. All neurofibromas expressed GHS-R, with a percentage of positive cells ranging from 4.9% to 76.1%. Large neurofibromas expressed more GHS-R than the small ones. The percentage of GHS-R-positive cells and intensity of GHS-R expression were positively correlated with neurofibromas volume. GHS-R expression was more common in female gender.

conclusionsGHS-R is expressed in cutaneous neurofibromas. Larger neurofibromas have a higher percentage of positive cells and higher GHS-R intensity. Based on our results we speculate that ghrelin may have an action on the tumorigenesis of cutaneous neurofibromas. Future studies are required to understand the role of ghrelin in the pathogenesis of NF1-associated cutaneous neurofibroma.

Indexed as

FemaleGhrelinHumansImmunohistochemistryMaleNeurofibromaNeurofibromatosis 1Receptors, GhrelinGhrelinReceptors, GhrelinGhrelinGhrelin receptorNeurofibromaNeurofibromatosis 1

Identifiers

PMID29262839
PMCPMC5738781
OpenAlexW2781433655

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.