Evidence map›Paper›PMID 26376656›Full record

ArticleJournal of neuro-oncology2016

Detecting the H3F3A mutant allele found in high-grade pediatric glioma by real-time PCR.

Ray Zhang, Jing Han, David Daniels, Haojie Huang, Zhiguo Zhang

Open access · greenAbstract read
In one paragraph

Article in Journal of neuro-oncology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

9 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Molecular Testing of Brain Tumor.Journal of pathology and translational medicine · 2017
    Review
  9. 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

5 authors at 2 institutions in 1 country.

Ray ZhangDepartment of Biochemistry and Molecular Biology, Mayo Clinic, 200 1ST SW, Rochester, MN, 55905, USA.
Jing HanDepartment of Biochemistry and Molecular Biology, Mayo Clinic, 200 1ST SW, Rochester, MN, 55905, USA.
David DanielsDepartment of Biochemistry and Molecular Biology, Mayo Clinic, 200 1ST SW, Rochester, MN, 55905, USA.
Haojie HuangDepartment of Biochemistry and Molecular Biology, Mayo Clinic, 200 1ST SW, Rochester, MN, 55905, USA.
Zhiguo ZhangDepartment of Biochemistry and Molecular Biology, Mayo Clinic, 200 1ST SW, Rochester, MN, 55905, USA. zhang.zhiguo@mayo.edu.
Mayo Clinic in Florida · USMayo Clinic · US

Funding

The role of a histone H4 phosphorylation in drug resistanceR01CA157489 · NCI · MAYO CLINIC ROCHESTER · PI ZHANG, ZHIGUO · 2012 to 2016
$1.6M
Uncovering Therapeutic Targets in Pediatric High Grade Gliomas with the H3K27M MutationK08NS092891 · NINDS · MAYO CLINIC ROCHESTER · PI DANIELS, DAVID · 2017 to 2021
$908k
NCI NIH HHS CA157489NCI NIH HHS R01 CA157489NINDS NIH HHS K08 NS092891
6 · The paper itself

Abstract

Diffuse intrinsic pontine glioma (DIPG) is an aggressive pediatric brain tumor with a median survival of 1 year after diagnosis. It has been reported recently that about 80% of DIPG cases and 70% of midline glioblastomas contain a mutation at one allele of the H3F3A gene (encoding histone H3 variant H3.3), replacing the lysine 27 with methionine (K27M). In order to facilitate diagnosis of DIPG patients, a quick and reliable method to identify the H3F3A K27M mutation is needed. Here, we describe a real-time PCR-based procedure involving a mutant-specific primer, a blocker oligonucleotide, and a reverse primer that can differentiate samples with H3F3A K27M mutation from those that do not. We first tested four different mutant-specific primers for their ability to selectively amplify H3F3A K27M-mutant allele and found that one primer amplified the mutant allele more efficiently than the rest. We then determined the optimal concentration of blocker oligo that significantly improved amplification of the H3F3A K27M-mutant allele. Using this optimized real-time PCR assay, we analyzed eleven samples, two of which containing H3F3A K27M mutation, and found that these two samples were differentially amplified from the nine others. In addition, we were able to discern the H3F3A K27M mutation in a newly obtained pediatric brainstem glioblastoma sample whose H3.3 status was not known previously, and in three other DIPG samples as well as paraffin embedded samples. These results demonstrate that we have developed a new reliable procedure for detecting the H3F3A K27M mutation in pediatric glioblastoma patient samples.

Indexed as

Real-Time Polymerase Chain ReactionAnimalsBrain NeoplasmsChildDNA Mutational AnalysisGene LibraryGliomaHistonesHumansLysineMaleMethionineMiceMutationTumor Cells, CulturedXenograft Model Antitumor AssaysH3-3A protein, humanHistonesLysineMethionineDiffuse intrinsic pontine gliomaHistone H3 variantPediatric glioblastomaReal-time PCR

Identifiers

PMID26376656
PMCPMC4859308
OpenAlexW1692474384

What OpenQuestion holds

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LicenceTDM
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.