Evidence map›Paper›PMID 30327548›Full record

ArticleScientific reports2018

Microglia induces Gas1 expression in human brain tumor-initiating cells to reduce tumorigenecity.

Susobhan Sarkar, Candice C Poon, Reza Mirzaei, Khalil S Rawji, Walter Hader, Pinaki Bose, John Kelly, Jeffrey F Dunn, V Wee Yong

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

11 citing papers in PubMed, 52 citations in OpenAlex.

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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

9 authors at 2 institutions in 1 country.

Susobhan SarkarDepartment of Clinical Neurosciences, Hotchkiss Brain Institute and the Arnie Charbonneau Cancer Institute University of Calgary, Calgary, Canada.
Candice C PoonDepartment of Clinical Neurosciences, Hotchkiss Brain Institute and the Arnie Charbonneau Cancer Institute University of Calgary, Calgary, Canada.
Reza MirzaeiDepartment of Clinical Neurosciences, Hotchkiss Brain Institute and the Arnie Charbonneau Cancer Institute University of Calgary, Calgary, Canada.
Khalil S RawjiDepartment of Clinical Neurosciences, Hotchkiss Brain Institute and the Arnie Charbonneau Cancer Institute University of Calgary, Calgary, Canada.
Walter HaderDepartment of Clinical Neurosciences, Hotchkiss Brain Institute and the Arnie Charbonneau Cancer Institute University of Calgary, Calgary, Canada.
Pinaki BoseDepartment of Biochemistry and Molecular Biology, Hotchkiss Brain Institute and the Arnie Charbonneau Cancer Institute University of Calgary, Calgary, Canada.
John KellyDepartment of Clinical Neurosciences, Hotchkiss Brain Institute and the Arnie Charbonneau Cancer Institute University of Calgary, Calgary, Canada.
Jeffrey F DunnDepartment of Radiology, Hotchkiss Brain Institute and the Arnie Charbonneau Cancer Institute University of Calgary, Calgary, Canada.
V Wee YongDepartment of Clinical Neurosciences, Hotchkiss Brain Institute and the Arnie Charbonneau Cancer Institute University of Calgary, Calgary, Canada. vyong@ucalgary.ca.
University of Calgary · CAOntario Brain Institute · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We reported previously that microglia decreased the growth of human brain tumor-initiating cells (BTICs). Through microarray analyses of BTICs exposed in vitro to microglia, we found the induction of several genes ascribed to have roles in cell cycle arrest, reduced cell proliferation and differentiation. Herein, we tested the hypothesis that one of these genes, growth arrest specific 1 (Gas1), is a novel growth reduction factor that is induced in BTICs by microglia. We found that microglia increased the expression of Gas1 transcript and protein in glioblastoma patient-derived BTIC lines. Using neurosphere assay we show that RNAi-induced reduction of Gas1 expression in BTICs blunted the microglia-mediated BTIC growth reduction. The role of Gas1 in mediating BTIC growth arrest was further validated using orthotopic brain xenografts in mice. When microglia-induced Gas1-expressing BTIC cells (mGas1-BTICs) were implanted intra-cranially in mice, tumor growth was markedly decreased; this was mirrored in the remarkable increase in survival of mGas1-BT025 and mGas1-BT048 implanted mice, compared to mice implanted with non-microglia-exposed BTIC cells. In conclusion, this study has identified Gas1 as a novel factor and mechanism through which microglia arrest the growth of BTICs for anti-tumor property.

Indexed as

AnimalsBrain NeoplasmsCell Cycle ProteinsCell Line, TumorCell Transformation, NeoplasticGlioblastomaGPI-Linked ProteinsHeterograftsHumansMiceMice, Inbred NODMice, SCIDMicrogliaNeoplastic Stem CellsCell Cycle ProteinsGAS1 protein, humanGPI-Linked Proteins

Identifiers

PMID30327548
PMCPMC6191418
OpenAlexW2896702493

What OpenQuestion holds

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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.