Evidence map›Paper›PMID 35713800›Full record

ArticleMolecular biology reports2022

NTRK2 gene fusions are uncommon in pilocytic astrocytoma.

Daniel Antunes Moreno, Aline Paixão Becker, Cristovam Scapulatempo-Neto, Weder Menezes, Jamie Sheren, Aline M Walter, Carlos Clara, Hélio R Machado, Ricardo S Oliveira, Luciano Neder and 2 more

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Article in Molecular biology reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 51% of its field
1 · What the graph read from it

What it found

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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

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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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
4 · The record

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5 · Who and what money

Authors and funding

12 authors at 5 institutions in 3 countries.

Daniel Antunes MorenoMolecular Oncology Research Center, Barretos Cancer Hospital, 1331 Antenor Duarte Vilela St, 14784-400, Barretos, SP, Brazil.
Aline Paixão BeckerJames Cancer Hospital and Solove Research Institute Columbus, Ohio, USA.
Cristovam Scapulatempo-NetoDepartment of Pathology, Barretos Cancer Hospital, Barretos, São Paulo, Brazil.
Weder MenezesMolecular Oncology Research Center, Barretos Cancer Hospital, 1331 Antenor Duarte Vilela St, 14784-400, Barretos, SP, Brazil.
Jamie SherenUniversity of Colorado School of Medicine, Aurora, CO, USA.
Aline M WalterUniversity of Colorado School of Medicine, Aurora, CO, USA.
Carlos ClaraDepartment of Neurosurgery, Barretos Cancer Hospital, 1331 Antenor Duarte Vilela St, 14784-400, Barretos, SP, Brazil.
Hélio R MachadoDepartment of Surgery, Ribeirao Preto, Brazil.
Ricardo S OliveiraDepartment of Surgery, Ribeirao Preto, Brazil.
Luciano NederDepartment of Pathology of Ribeirão Preto Medical School, University of São Paulo (FMRP-USP) - Campus of University of Sao Paulo, 14049-900, Ribeirao Preto, SP, Brazil.
Marileila Varella-GarciaUniversity of Colorado School of Medicine, Aurora, CO, USA.
Rui Manuel ReisMolecular Oncology Research Center, Barretos Cancer Hospital, 1331 Antenor Duarte Vilela St, 14784-400, Barretos, SP, Brazil. ruireis.hcb@gmail.com.ORCID http://orcid.org/0000-0002-9639-7940
Hospital de Câncer de Barretos · BRUniversity of Colorado Anschutz Medical Campus · USClinics Hospital of Ribeirão Preto · BRThe Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute · USUniversidade de Ribeirão Preto · BR

Funding

Coordination for the Improvement of Level Personnel (CAPES, Brazil) Coordination for the Improvement of Level Personnel (CAPES, Brazil)National Council for Scientific and Technological Development CNPq- 475358/2011-2NIH-P30CA046934 (CCSG Molecular Pathology/Cytogenetics) NIH-P30CA046934 (CCSG Molecular Pathology/Cytogenetics)São Paulo Foundation for Research Support FAPESP -2012/19590-0
6 · The paper itself

Abstract

backgroundPilocytic astrocytoma is the most frequent pediatric glioma. Despite its overall good prognosis, complete surgical resection is sometimes unfeasible, especially for patients with deep-seated tumors. For these patients, the identification of targetable genetic alterations such as NTRK fusions, raised as a new hope for therapy. The presence of gene fusions involving NTRK2 has been rarely reported in pilocytic astrocytoma. The aim of the present study was to investigate the frequency of NTRK2 alterations in a series of Brazilian pilocytic astrocytomas.

methodsSixty-nine pilocytic astrocytomas, previously characterized for BRAF and FGFR1 alterations were evaluated. The analysis of NTRK2 alterations was performed using a dual color break apart fluorescence in situ hybridization (FISH) assay.

resultsNTRK2 fusions were successfully evaluated by FISH in 62 of the 69 cases. Neither evidence of NTRK2 gene rearrangements nor NTRK2 copy number alterations were found.

conclusionsNTRK2 alterations are uncommon genetic events in pilocytic astrocytomas, regardless of patients' clinicopathological and molecular features.

Indexed as

AstrocytomaBrain NeoplasmsGliomaGene FusionHumansIn Situ Hybridization, FluorescenceProto-Oncogene Proteins B-rafProto-Oncogene Proteins B-rafFISH.Gene fusionsNTRK2Pilocytic astrocytomaTyrosine kinases

Identifiers

PMID35713800
OpenAlexW4283069295

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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.