Evidence map›Paper›PMID 33768215›Full record

ArticleJournal of experimental neurology2020

A Protocol for the Generation of Treatment-naïve Biopsy-derived Diffuse Intrinsic Pontine Glioma and Diffuse Midline Glioma Models.

Matt C Biery, Alyssa Noll, Carrie Myers, Shelli M Morris, Conrad A Winter, Fiona Pakiam, Bonnie L Cole, Samuel R Browd, James M Olson, Nicholas A Vitanza

Open access · hybridAbstract read
In one paragraph

Article in Journal of experimental neurology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-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

10 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
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  6. Article
  7. [Pediatric posterior fossa tumors].Radiologie (Heidelberg, Germany) · 2023
    Review
  8. Review
  9. Article
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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.

Matt C BieryFred Hutchinson Cancer Research Center, Seattle, WA, USA.
Alyssa NollFred Hutchinson Cancer Research Center, Seattle, WA, USA.
Carrie MyersFred Hutchinson Cancer Research Center, Seattle, WA, USA.
Shelli M MorrisFred Hutchinson Cancer Research Center, Seattle, WA, USA.
Conrad A WinterFred Hutchinson Cancer Research Center, Seattle, WA, USA.
Fiona PakiamFred Hutchinson Cancer Research Center, Seattle, WA, USA.
Bonnie L ColeDepartment of Laboratories, Seattle Children's Hospital, Seattle, WA, USA.
Samuel R BrowdDivision of Neurosurgery, Department of Neurological Surgery, University of Washington, Seattle Children's Hospital, Seattle, WA, USA.
James M OlsonFred Hutchinson Cancer Research Center, Seattle, WA, USA.
Nicholas A VitanzaFred Hutchinson Cancer Research Center, Seattle, WA, USA.
Fred Hutch Cancer Center · USUniversity of Washington · USSeattle Children's Hospital · US

Funding

Testing a cancer patient-specific SARS-CoV-2 vaccine in chemotherapy- and radiation-treated pediatric brain tumor mouse modelsR01CA114567 · NCI · SEATTLE CHILDREN'S HOSPITAL · PI OLSON, JAMES M · 2006 to 2023
$4.9M
Combinations of Synergistic Bispecific Human Antibodies: A Novel Strategy for the Treatment of NeuroblastomaU01CA232490 · NCI · SEATTLE CHILDREN'S HOSPITAL · PI OLSON, JAMES M · 2018 to 2020
$2.4M
NCI NIH HHS R01 CA114567NCI NIH HHS U01 CA232490
6 · The paper itself

Abstract

Diffuse intrinsic pontine glioma (DIPG) is a universally fatal tumor of the brainstem, most commonly affecting young children. Due to its location, surgical resection is not achievable, but consideration of a biopsy has become standard practice at children's hospitals with the appropriate neurosurgical expertise. While the decision to obtain a biopsy should be directed by the presence of atypical radiographic features that call the diagnosis of DIPG into question or the requirement of biopsy tissue for clinical trial enrollment, once this precious tissue is available its use for research should be considered. The majority of DIPG and diffuse midline glioma, H3 K27M-mutant (DMG) models are autopsy-derived or genetically-engineered, each of which has limitations for translational studies, so the use of biopsy tissue for laboratory model development provides an opportunity to create unique model systems. Here, we present a detailed laboratory protocol for the generation of treatment-naïve biopsy-derived DIPG/DMG models.

Identifiers

PMID33768215
PMCPMC7990285
OpenAlexW3127678880

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.