Evidence map›Paper›PMID 31540507›Full record

ArticleInternational journal of molecular sciences2019

The Evaluation of Glioblastoma Cell Dissociation and Its Influence on Its Behavior.

Veronika Skarkova, Marketa Krupova, Barbora Vitovcova, Adam Skarka, Petra Kasparova, Petr Krupa, Vera Kralova, Emil Rudolf

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2019. 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
–field-weighted citation impact
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.

  1. Article
  2. Article
  3. Review
  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

8 authors.

Veronika SkarkovaDepartment of Medical Biology and Genetics, Faculty of Medicine, Charles University, Simkova 870, CZ-500 38 Hradec Kralove, Czech Republic. hanusovav@lfhk.cuni.cz.
Marketa KrupovaThe Fingerland Department of Pathology, Faculty of Medicine and University Hospital in Hradec Kralove, Charles University, Sokolska 581, CZ-500 05 Hradec Kralove, Czech Republic. marketa.valkova@fnhk.cz.
Barbora VitovcovaDepartment of Medical Biology and Genetics, Faculty of Medicine, Charles University, Simkova 870, CZ-500 38 Hradec Kralove, Czech Republic. vitovcob@lfhk.cuni.cz.
Adam SkarkaDepartment of Chemistry, Faculty of Sciences, University of Hradec Kralove, Hradecka 1285, CZ-500 03 Hradec Kralove, Czech Republic. adam.skarka@uhk.cz.
Petra KasparovaThe Fingerland Department of Pathology, Faculty of Medicine and University Hospital in Hradec Kralove, Charles University, Sokolska 581, CZ-500 05 Hradec Kralove, Czech Republic. petra.kasparova@fnhk.cz.
Petr KrupaDepartment of Neurosurgery, Faculty of Medicine and University Hospital in Hradec Kralove, Charles University, Sokolska 581, CZ-500 05 Hradec Kralove, Czech Republic. petr.krupa@fnhk.cz.
Vera KralovaDepartment of Medical Biology and Genetics, Faculty of Medicine, Charles University, Simkova 870, CZ-500 38 Hradec Kralove, Czech Republic. kralovav@lfhk.cuni.cz.
Emil RudolfDepartment of Medical Biology and Genetics, Faculty of Medicine, Charles University, Simkova 870, CZ-500 38 Hradec Kralove, Czech Republic. rudolf@lfhk.cuni.cz.ORCID 0000-0002-9526-3174

Funding

Grantová Agentura, Univerzita Karlova GAUK No. 460217Univerzita Hradec Kralove, Fakulta přírodních věd VT2019Univerzita Karlova, Lékařská fakulta v Hradci Králové PROGRES Q40/01Univerzita Karlova, Lékařská fakulta v Hradci Králové PROGRES Q40/11
6 · The paper itself

Abstract

purposePrimary cell lines are a valuable tool for evaluation of tumor behavior or sensitivity to anticancer treatment and appropriate dissociation of cells could preserve genomic profile of the original tissue. The main aim of our study was to compare the influence of two methods of glioblastoma multiforme (GBM) cell derivation (mechanic-MD; enzymatic-ED) on basic biological properties of thus derived cells and correlate them to the ones obtained from stabilized GBM cell line A-172.

methodsCell proliferation and migration (xCELLigence Real-Time Cell Analysis), expression of microRNAs and protein markers (RT-PCR and Western blotting), morphology (phase contrast and fluorescent microscopy), and accumulation of temozolomide (TMZ) and its metabolite 5-aminoimidazole-4-carboxamide (AIC) inside the cells (LC-MS analysis) were carried out in five different samples of GBM (GBM1, GBM2, GBM32, GBM33, GBM34), with each of them processed by MD and ED types of isolations. The same analyses were done in the A-172 cell line too.

resultsPrimary GBM cells obtained by ED or MD approaches significantly differ in biological behavior and properties of these cells. Unlike in primary MD GBM cells, higher proliferation, as well as migration, was observed in primary ED GBM cells, which were also associated with the acquired mesenchymal phenotype and higher sensitivity to TMZ. Finally, the same analyses of stabilized GBM cell line A-172 revealed several important differences in measured parameters.

conclusionsGBM cells obtained by MD and ED dissociation show considerable heterogeneity, but based on our results, MD approach should be the preferred method of primary GBM cell isolation.

Indexed as

Cell MovementCell ProliferationAntineoplastic Agents, AlkylatingBrain NeoplasmsCell Line, TumorCell SeparationDrug Resistance, NeoplasmDrug Screening Assays, AntitumorGene Expression Regulation, NeoplasticGlioblastomaHumansTemozolomideTumor Cells, CulturedAntineoplastic Agents, AlkylatingTemozolomidecell isolationglioblastoma multiformeresistancetemozolomide

Identifiers

PMID31540507
PMCPMC6770747

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Registered trials

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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.