Evidence map›Paper›PMID 36008944›Full record

ArticleBiomolecules2022

Glioblastoma Stem-Like Cells (GSCs) with Mesenchymal Signature: Lipid Profiles of Mobile Lipids Obtained with MRS before and after Radio/Chemical Treatments.

Sveva Grande, Alessandra Palma, Anna Maria Luciani, Pasqualino Anello, Lucia Ricci-Vitiani, Mariachiara Buccarelli, Quintino Giorgio D'Alessandris, Roberto Pallini, Laura Guidoni, Vincenza Viti and 1 more

Open access · goldAbstract read
In one paragraph

Article in Biomolecules, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 46% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
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 3 institutions in 1 country.

Sveva GrandeNational Centre for Innovative Technologies in Public Health, Istituto Superiore di Sanità, 00161 Rome, Italy.ORCID 0000-0002-1925-7602
Alessandra PalmaNational Centre for Innovative Technologies in Public Health, Istituto Superiore di Sanità, 00161 Rome, Italy.ORCID 0000-0002-8530-4913
Anna Maria LucianiNational Centre for Innovative Technologies in Public Health, Istituto Superiore di Sanità, 00161 Rome, Italy.
Pasqualino AnelloNational Centre for Innovative Technologies in Public Health, Istituto Superiore di Sanità, 00161 Rome, Italy.
Lucia Ricci-VitianiDepartment of Oncology and Molecular Medicine, Istituto Superiore di Sanità, 00161 Rome, Italy.
Mariachiara BuccarelliDepartment of Oncology and Molecular Medicine, Istituto Superiore di Sanità, 00161 Rome, Italy.ORCID 0000-0003-1157-4694
Quintino Giorgio D'AlessandrisInstitute of Neurosurgery, Fondazione IRCCS Policlinico Universitario A. Gemelli, 00168 Rome, Italy.ORCID 0000-0002-2953-9291
Roberto PalliniInstitute of Neurosurgery, Fondazione IRCCS Policlinico Universitario A. Gemelli, 00168 Rome, Italy.ORCID 0000-0002-4611-8827
Laura GuidoniNational Centre for Innovative Technologies in Public Health, Istituto Superiore di Sanità, 00161 Rome, Italy.
Vincenza VitiNational Centre for Innovative Technologies in Public Health, Istituto Superiore di Sanità, 00161 Rome, Italy.
Antonella RosiNational Centre for Innovative Technologies in Public Health, Istituto Superiore di Sanità, 00161 Rome, Italy.
Istituto Superiore di Sanità · ITAgostino Gemelli University Polyclinic · ITUniversità Cattolica del Sacro Cuore · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma is the most common and lethal primary malignant brain tumor in adults. Glioblastoma stem cells (GSCs) promote and are responsible for glioblastoma intratumoral heterogeneity and therapy resistance, due to their two main features: self-renewal and differentiation. Lipids have important biological and physiological functions that are critical for understanding the regulation and control of stem cell fate; lipid metabolism and related unsaturation levels play a possible role as the target of therapeutics to overcome glioblastoma radioresistance. This paper aimed at an in-depth analysis of 13 GSC mesenchymal (MES) lines, two subclones, and a stabilized glioblastoma line (T98G) by magnetic resonance spectroscopy (MRS). Particularly, 2D MRS was used to investigate lipid unsaturation behavior during growth in culture and after treatment with etomoxir and photon beams. MES lines, although belonging to the same genetic and metabolic cluster, showed metabolic heterogeneity when observed by MRS, focusing on lipid signals. Nonetheless, the observed unsaturation level stability for two representative lines after stressful treatments suggests unusual robustness of the unsaturation levels for each line, as a peculiar and intrinsic characteristic of GSCs.

Indexed as

Brain NeoplasmsGlioblastomaHumansLipidsMagnetic Resonance SpectroscopyNeoplastic Stem CellsLipidsglioblastomalipidsmesenchymal stem cellsMR spectroscopyunsaturation

Identifiers

PMID36008944
PMCPMC9405836
OpenAlexW4288439489

What Socratic 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 Socratic graph.