Evidence map›Paper›PMID 29888503›Full record

ArticleThe Journal of pathology2018

Elevation of the TP53 isoform Δ133p53β in glioblastomas: an alternative to mutant p53 in promoting tumor development.

Marina Kazantseva, Ramona A Eiholzer, Sunali Mehta, Ahmad Taha, Sara Bowie, Imogen Roth, Jean Zhou, Sebastien M Joruiz, Janice A Royds, Noelyn A Hung and 2 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of pathology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

35 citing papers in PubMed, 40 citations in OpenAlex.

  1. The p53 Isoforms as Potential Biomarkers in Different Cancer Entities.International journal of molecular sciences · 2026
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  13. p53 Dysregulation in Breast Cancer: Insights on Mutations in theInternational journal of molecular sciences · 2023
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  16. Increased Expression of the Δ133p53β Isoform Enhances Brain Metastasis.International journal of molecular sciences · 2023
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  17. p53 Family in Resistance to Targeted Therapy of Melanoma.International journal of molecular sciences · 2022
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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

12 authors at 4 institutions in 2 countries.

Marina KazantsevaDepartment of Pathology, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand.
Ramona A EiholzerDepartment of Pathology, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand.
Sunali MehtaDepartment of Pathology, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand.
Ahmad TahaDepartment of Neurosurgery, Southern District Heath Board, New Zealand.
Sara BowieDepartment of Pathology, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand.
Imogen RothDepartment of Pathology, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand.
Jean ZhouDepartment of Pathology, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand.
Sebastien M JoruizJacqui Wood Cancer Centre, Division of Cancer Research, University of Dundee, UK.ORCID 0000-0002-5613-2665
Janice A RoydsDepartment of Pathology, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand.
Noelyn A HungDepartment of Pathology, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand.
Tania L SlatterDepartment of Pathology, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand.ORCID 0000-0003-4031-0604
Antony W BraithwaiteDepartment of Pathology, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand.
University of Otago · NZMaurice Wilkins Centre · NZSouthern District Health Board · NZUniversity of Dundee · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As tumor protein 53 (p53) isoforms have tumor-promoting, migration, and inflammatory properties, this study investigated whether p53 isoforms contributed to glioblastoma progression. The expression levels of full-length TP53α (TAp53α) and six TP53 isoforms were quantitated by RT-qPCR in 89 glioblastomas and correlated with TP53 mutation status, tumor-associated macrophage content, and various immune cell markers. Elevated levels of Δ133p53β mRNA characterised glioblastomas with increased CD163-positive macrophages and wild-type TP53. In situ-based analyses found Δ133p53β expression localised to malignant cells in areas with increased hypoxia, and in cells with the monocyte chemoattractant protein C-C motif chemokine ligand 2 (CCL2) expressed. Tumors with increased Δ133p53β had increased numbers of cells positive for macrophage colony-stimulating factor 1 receptor (CSF1R) and programmed death ligand 1 (PDL1). In addition, cells expressing a murine 'mimic' of Δ133p53 (Δ122p53) were resistant to temozolomide treatment and oxidative stress. Our findings suggest that elevated Δ133p53β is an alternative pathway to TP53 mutation in glioblastoma that aids tumor progression by promoting an immunosuppressive and chemoresistant environment. Adding Δ133p53β to a TP53 signature along with TP53 mutation status will better predict treatment resistance in glioblastoma. © 2018 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland.

Indexed as

AnimalsAntigens, CDAntigens, Differentiation, MyelomonocyticAntineoplastic Agents, AlkylatingB7-H1 AntigenBiomarkers, TumorBrain NeoplasmsCD163 AntigenCell LineChemokine CCL2Drug Resistance, NeoplasmGene Expression Regulation, NeoplasticGlioblastomaHumansMacrophagesMiceAntigens, CDAntigens, Differentiation, MyelomonocyticAntineoplastic Agents, AlkylatingB7-H1 AntigenBiomarkers, TumorCCL2 protein, humanCD163 AntigenCD274 protein, humanChemokine CCL2CSF1R protein, humanProtein IsoformsReceptor, Macrophage Colony-Stimulating FactorReceptors, Cell SurfaceReceptors, Granulocyte-Macrophage Colony-Stimulating FactorTemozolomideTP53 protein, humanTumor Suppressor Protein p53CSF1Rglioblastomamutant TP53PDL1TP53 isoformtumor-associated macrophagesΔ133p53β

Identifiers

PMID29888503
PMCPMC6120556
OpenAlexW2808261954

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.