Evidence map›Paper›PMID 27230828›Full record

ArticleScientific reports2016

Identifications of novel mechanisms in breast cancer cells involving duct-like multicellular spheroid formation after exposure to the Random Positioning Machine.

Sascha Kopp, Lasse Slumstrup, Thomas J Corydon, Jayashree Sahana, Ganna Aleshcheva, Tawhidul Islam, Nils E Magnusson, Markus Wehland, Johann Bauer, Manfred Infanger and 1 more

Abstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing 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

55 citing papers in PubMed.

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  11. Omics Studies of Tumor Cells under Microgravity Conditions.International journal of molecular sciences · 2024
    Review
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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.

Sascha KoppClinic for Plastic, Aesthetic and Hand Surgery, Otto-von Guericke-University, D-39120 Magdeburg, Germany.
Lasse SlumstrupDepartment of Biomedicine, Aarhus University, DK-8000 Aarhus C, Denmark.
Thomas J CorydonDepartment of Biomedicine, Aarhus University, DK-8000 Aarhus C, Denmark.
Jayashree SahanaDepartment of Biomedicine, Aarhus University, DK-8000 Aarhus C, Denmark.
Ganna AleshchevaClinic for Plastic, Aesthetic and Hand Surgery, Otto-von Guericke-University, D-39120 Magdeburg, Germany.
Tawhidul IslamDepartment of Biomedicine, Aarhus University, DK-8000 Aarhus C, Denmark.
Nils E MagnussonMedical Research Laboratory, Department of Clinical Medicine, Aarhus University, DK-8000 Aarhus C, Denmark.
Markus WehlandClinic for Plastic, Aesthetic and Hand Surgery, Otto-von Guericke-University, D-39120 Magdeburg, Germany.
Johann BauerMax-Planck-Institute of Biochemistry, D-82152 Martinsried, Germany.
Manfred InfangerClinic for Plastic, Aesthetic and Hand Surgery, Otto-von Guericke-University, D-39120 Magdeburg, Germany.
Daniela GrimmClinic for Plastic, Aesthetic and Hand Surgery, Otto-von Guericke-University, D-39120 Magdeburg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many cell types form three-dimensional aggregates (MCS; multicellular spheroids), when they are cultured under microgravity. MCS often resemble the organ, from which the cells have been derived. In this study we investigated human MCF-7 breast cancer cells after a 2 h-, 4 h-, 16 h-, 24 h- and 5d-exposure to a Random Positioning Machine (RPM) simulating microgravity. At 24 h few small compact MCS were detectable, whereas after 5d many MCS were floating in the supernatant above the cells, remaining adherently (AD). The MCS resembled the ducts formed in vivo by human epithelial breast cells. In order to clarify the underlying mechanisms, we harvested MCS and AD cells separately from each RPM-culture and measured the expression of 29 selected genes with a known involvement in MCS formation. qPCR analyses indicated that cytoskeletal genes were unaltered in short-term samples. IL8, VEGFA, and FLT1 were upregulated in 2 h/4 h AD-cultures. The ACTB, TUBB, EZR, RDX, FN1, VEGFA, FLK1 Casp9, Casp3, PRKCA mRNAs were downregulated in 5d-MCS-samples. ESR1 was upregulated in AD, and PGR1 in both phenotypes after 5d. A pathway analysis revealed that the corresponding gene products are involved in organization and regulation of the cell shape, in cell tip formation and membrane to membrane docking.

Indexed as

Gene Expression RegulationCell MembraneCytoskeletal ProteinsEstrogen Receptor alphaHumansInterleukin-8Intracellular Signaling Peptides and ProteinsMCF-7 CellsNuclear ProteinsPhenotypeProtein Interaction MappingSignal TransductionSpheroids, CellularVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-1Weightlessness SimulationCXCL8 protein, humanCytoskeletal ProteinsESR1 protein, humanEstrogen Receptor alphaFLT1 protein, humanInterleukin-8Intracellular Signaling Peptides and ProteinsMRFAP1 protein, humanNuclear ProteinsVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-1VEGFA protein, human

Identifiers

PMID27230828
PMCPMC4882535

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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.