Evidence map›Paper›PMID 25883769›Full record

ArticleClinical and translational medicine2015

Incidence of kiaa1549-braf fusion gene in Egyptian pediatric low grade glioma.

Hala Taha, Maha Yehia, Madeha Mahmoud, Mohamed El-Beltagy, Myret Ghabriel, Shahenda El-Naggar

Open access · goldAbstract read
In one paragraph

Article in Clinical and translational medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

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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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Pilocytic astrocytomas: BRAFV600E and BRAF fusion expression patterns in pediatric and adult age groups.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2019
    Article
  4. Article
  5. Article
  6. An integrative molecular and genomic analysis of pediatric hemispheric low-grade gliomas: an update.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2016
    Review
  7. Article
  8. 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

6 authors at 1 institution in 1 country.

Hala TahaDepartment of Pathology, Children's Cancer Hospital Egypt 57357, P.O Box 11441, 1 Sekeat El-Imam, Cairo, Egypt.
Maha YehiaDepartment of Pathology, Children's Cancer Hospital Egypt 57357, P.O Box 11441, 1 Sekeat El-Imam, Cairo, Egypt.
Madeha MahmoudDepartment of Pediatric Oncology, Children's Cancer Hospital Egypt 57357, P.O Box 11441, 1 Sekeat El-Imam, Cairo, Egypt.
Mohamed El-BeltagyDepartment of Neurosurgery, Children's Cancer Hospital Egypt 57357, P.O Box 11441, 1 Sekeat El-Imam, Cairo, Egypt.
Myret GhabrielBasic Research Department, Children's Cancer Hospital Egypt 57357, P.O Box 11441, 1 Sekeat El-Imam, Cairo, Egypt.
Shahenda El-NaggarBasic Research Department, Children's Cancer Hospital Egypt 57357, P.O Box 11441, 1 Sekeat El-Imam, Cairo, Egypt.
Children Cancer Hospital · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLow grade gliomas are the most common brain tumor in children. Tandem duplication involving the KIAA1549 and the BRAF kinase genes results in a gene fusion that has been recently characterized in a subset of low grade glioma While there is no clear evidence that the KIAA1549-BRAF gene fusion has an effect on prognosis, it is an attractive target for therapy development and as a diagnostic tool.

methodsIn the current study we examine the prevalence of KIAA1549-BRAF gene fusion in pediatric patients diagnosed with low grade glioma in the Egyptian population and its relationship to clinical and histological subtypes. Sixty patients between the ages of 1 to 18 years were analyzed for the presence of KIAA1549-BRAF fusion gene products using reverse transcription-PCR and sequencing. The clinicopathologic tumor characteristics were then analyzed in relation to the different fusion genes.

resultsKIAA1549-BRAF fusion genes were detected in 56.6% of patients. They were primarily associated with pilocytic astrocytoma (74.2%) and pilomyxoid astrocytoma (60%). Translocation 15-9 was the most common, representing (55.8%) of all positive samples followed by 16-9 (26.4%) and 16-11 (8.8%). Pilocytic astrocytomas presented primarily with 15-9 (32.2%), 16-9 (25.8%) and 16-11 (6.4%) while pilomyxoid astrocytomas presented with 15-9 (46.6%), 16-9 (6.6%) and 16-11 (6.6%) translocations.

conclusionGene fusion is found to be significantly increased in cerebellar pilocytic astrocytoma tumors. Furthermore, 15-9 was found to have a higher incidence among our cohort compared to previous studies. While most of the gene fusion positive pilomyxoid astrocytomas were 15-9, we find the association none significant.

Indexed as

BRAFCancerGene fusionGliomaKIAA1549

Identifiers

PMID25883769
PMCPMC4392037
OpenAlexW2152219836

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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.