Evidence map›Paper›PMID 29713042›Full record

ArticleModern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc2018

Endothelial trans-differentiation in glioblastoma recurring after radiotherapy.

Ivana De Pascalis, Liliana Morgante, Simone Pacioni, Quintino Giorgio D'Alessandris, Stefano Giannetti, Maurizio Martini, Lucia Ricci-Vitiani, Matteo Malinverno, Elisabetta Dejana, Luigi M Larocca and 1 more

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In one paragraph

Article in Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.5field-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

21 citing papers in PubMed, 42 citations in OpenAlex.

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  12. Tumor Vessels Fuel the Fire in Glioblastoma.International journal of molecular sciences · 2021
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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

11 authors at 2 institutions in 1 country.

Ivana De PascalisInstitute of Neurosurgery, Università Cattolica del Sacro Cuore, Rome, Italy.
Liliana MorganteInstitute of Human Anatomy, Università Cattolica del Sacro Cuore, Rome, Italy.
Simone PacioniInstitute of Neurosurgery, Università Cattolica del Sacro Cuore, Rome, Italy.
Quintino Giorgio D'AlessandrisInstitute of Neurosurgery, Università Cattolica del Sacro Cuore, Rome, Italy.
Stefano GiannettiInstitute of Human Anatomy, Università Cattolica del Sacro Cuore, Rome, Italy.
Maurizio MartiniInstitute of Pathology, Università Cattolica del Sacro Cuore, Rome, Italy.
Lucia Ricci-VitianiDepartment of Oncology and Molecular Medicine, Istituto Superiore di Sanità, Rome, Italy.
Matteo MalinvernoNew Strategies to Inhibit Tumor Angiogenesis Program Fondazione Italiana per la Ricerca sul Cancro, Institute of Molecular Oncology Fondazione, Milan, Italy.
Elisabetta DejanaNew Strategies to Inhibit Tumor Angiogenesis Program Fondazione Italiana per la Ricerca sul Cancro, Institute of Molecular Oncology Fondazione, Milan, Italy.
Luigi M LaroccaInstitute of Pathology, Università Cattolica del Sacro Cuore, Rome, Italy.ORCID http://orcid.org/0000-0003-1739-4758
Roberto PalliniInstitute of Neurosurgery, Università Cattolica del Sacro Cuore, Rome, Italy. roberto.pallini@unicatt.it.
Università Cattolica del Sacro Cuore · ITIstituto Superiore di Sanità · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We hypothesized that in glioblastoma recurring after radiotherapy, a condition whereby the brain endothelium undergoes radiation-induced senescence, tumor cells with endothelial phenotype may be relevant for tumor neovascularization. Matched glioblastoma samples obtained at primary surgery and at surgery for tumor recurrence after radiotherapy, all expressing epidermal growth factor receptor variant III (EGFRvIII), were assessed by a technique that combines fluorescent in situ hybridization (FISH) for the EGFR/CEP7 chromosomal probe with immunostaining for endothelial cells (CD31) and activated pericytes (α Smooth Muscle Actin). Five EGFRvIII-expressing paired primary/recurrent glioblastoma samples, in which the tumor cells showed EGFR/CEP7 amplification, were then assessed by CD31 and α Smooth Muscle Actin immunofluorescence. In glomeruloid bodies, the ratio between CD31+ cells with amplified EGFR/CEP7 signal and the total CD31+ cells was 0.23 ± 0.09 (mean ± sem) and 0.63 ± 0.07 in primary tumors and in recurrent ones, respectively (p < 0.002, Student-t test). In capillaries, the ratio of CD31+ cells with amplified EGFR/CEP7 over the total CD31+ cells lining the capillary lumen was 0.21 ± 0.06 (mean ± sem) and 0.42 ± 0.07 at primary surgery and at recurrence, respectively (p < 0.005, Student-t test). Expression of α Smooth Muscle Actin by cells with EGFR/CEP7 amplification was not observed. Then, in glioblastoma recurring after radiotherapy, where the brain endothelium suffers from radiation-induced cell senescence, tumor-derived endothelium plays a role in neo-vascularization.

Indexed as

AnimalsBrain NeoplasmsCell TransdifferentiationEndothelial CellsErbB ReceptorsGlioblastomaHumansHuman Umbilical Vein Endothelial CellsIn Situ Hybridization, FluorescenceMiceNeoplasm Recurrence, LocalErbB Receptors

Identifiers

PMID29713042
OpenAlexW2802491296

What OpenQuestion holds

Textmetadata
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.