Evidence map›Paper›PMID 30990879›Full record

ArticleJournal of neuropathology and experimental neurology2019

Differential Expression of Wilms' Tumor Protein in Diffuse Intrinsic Pontine Glioma.

Sulgi Lee, Madhuri Kambhampati, Sridevi Yadavilli, Heather Gordish-Dressman, Mariarita Santi, Conrad R Cruz, Roger J Packer, M Isabel Almira-Suarez, Eugene I Hwang, Javad Nazarian

Open access · bronzeAbstract read
In one paragraph

Article in Journal of neuropathology and experimental neurology, 2019. 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
0.4field-weighted citation impact, top 39% 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

8 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Practical immunomodulatory landscape of glioblastoma multiforme (GBM) therapy.Journal of the Egyptian National Cancer Institute · 2024
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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 2 institutions in 1 country.

Sulgi LeeChildren's National Health System, Center for Genetic Medicine Research, Washington, District of Columbia.
Madhuri KambhampatiChildren's National Health System, Center for Genetic Medicine Research, Washington, District of Columbia.
Sridevi YadavilliChildren's National Health System, Center for Genetic Medicine Research, Washington, District of Columbia.
Heather Gordish-DressmanChildren's National Health System, Center for Genetic Medicine Research, Washington, District of Columbia.
Mariarita SantiDepartment of Pathology, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Conrad R CruzChildren's National Health System, Center for Cancer and Immunology Research, Washington, District of Columbia.
Roger J PackerChildren's National Health System, Brain Tumor Institute, Washington, District of Columbia.
M Isabel Almira-SuarezDepartment of Pathology and Laboratory Medicine, Children's National Health System, Washington, District of Columbia (MIA-S).
Eugene I HwangChildren's National Health System, Brain Tumor Institute, Washington, District of Columbia.
Javad NazarianChildren's National Health System, Center for Genetic Medicine Research, Washington, District of Columbia.
Children's National · USChildren's Hospital of Philadelphia · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diffuse intrinsic pontine gliomas (DIPGs) are deadly tumors comprising 10%-15% of all childhood CNS cancers. Standard treatment is considered palliative and prognosis is near universal mortality. DIPGs have been classified into genomic subtypes based on histone variants with the lysine to methionine mutation on position 27 of histone tails (K27M). Given the increasing promise of immunotherapy, there have been ongoing efforts to identify tumor-specific antigens to serve as immunologic targets. We evaluated a large cohort of CNS specimens for Wilms' tumor protein (WT1) expression. These specimens include primary pediatric CNS tumors (n = 38 midline gliomas and n = 3 non-midline gliomas; n = 23 DIPG, n = 10 low-grade gliomas, n = 8 high-grade gliomas), and DIPG primary cells. Here, we report the validation of WT1 as a tumor-associated antigen in DIPGs. We further report that WT1 expression is significantly correlated with specific oncohistone variants, with the highest expression detected in the H3.3K27M subgroup. WT1 expression was absent in all control specimens (n = 21). Western blot assays using DIPG primary cells (n = 6) showed a trend of higher WT1 expression in H3.3K27M cells when compared with H3.1 K27M cells and H3 wildtype cells. Our data are the first indication of the association between WT1 and DIPG, with specific upregulation in those harboring oncohistone H3.3K27M.

Indexed as

Gene Expression Regulation, NeoplasticAdolescentBrain Stem NeoplasmsChildChild, PreschoolCohort StudiesDiffuse Intrinsic Pontine GliomaFemaleHumansInfantMaleMutationWT1 ProteinsYoung AdultWT1 protein, humanWT1 ProteinsBrainstem gliomaChildhood midline gliomaDiffuse intrinsic pontine glioma (DIPG)Wilms tumor protein (WT1)

Identifiers

PMID30990879
PMCPMC6467196
OpenAlexW2937732940

What OpenQuestion holds

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LicenceCC BY-NC
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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 OpenQuestion graph.