Evidence map›Paper›PMID 26167936›Full record

ArticlePloS one2015

ROCK Inhibition Facilitates In Vitro Expansion of Glioblastoma Stem-Like Cells.

Samantha G Tilson, Elizabeth M Haley, Ursula L Triantafillu, David A Dozier, Catherine P Langford, G Yancey Gillespie, Yonghyun Kim

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.2field-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

26 citing papers in PubMed, 38 citations in OpenAlex.

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  12. Rho Kinases in Embryonic Development and Stem Cell Research.Archivum immunologiae et therapiae experimentalis · 2022
    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

7 authors at 2 institutions in 1 country.

Samantha G TilsonDepartment of Chemical and Biological Engineering, The University of Alabama, Tuscaloosa, Alabama, United States of America.
Elizabeth M HaleyDepartment of Chemical and Biological Engineering, The University of Alabama, Tuscaloosa, Alabama, United States of America.
Ursula L TriantafilluDepartment of Chemical and Biological Engineering, The University of Alabama, Tuscaloosa, Alabama, United States of America.
David A DozierDepartment of Chemical and Biological Engineering, The University of Alabama, Tuscaloosa, Alabama, United States of America.
Catherine P LangfordDepartment of Neurosurgery, The University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
G Yancey GillespieDepartment of Neurosurgery, The University of Alabama at Birmingham, Birmingham, Alabama, United States of America.
Yonghyun KimDepartment of Chemical and Biological Engineering, The University of Alabama, Tuscaloosa, Alabama, United States of America.
University of Alabama · USUniversity of Alabama at Birmingham · US

Funding

CONTEMPORARY THERAPEUTICS FOR ANAPLASTIC GLIOMASP20CA151129 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI GILLESPIE, G. YANCEY · 2011 to 2013
$2.3M
NCI NIH HHS P20 CA151129
6 · The paper itself

Abstract

Due to their stem-like characteristics and their resistance to existing chemo- and radiation therapies, there is a growing appreciation that cancer stem cells (CSCs) are the root cause behind cancer metastasis and recurrence. However, these cells represent a small subpopulation of cancer cells and are difficult to propagate in vitro. Glioblastoma is an extremely deadly form of brain cancer that is hypothesized to have a subpopulation of CSCs called glioblastoma stem cells (GSCs; also called brain tumor initiating cells, BTICs). We propose the use of selective Rho-kinase (ROCK) inhibitors, Y-27632 and fasudil, to promote GSC/BTIC-like cell survival and propagation in vitro. ROCK inhibitors have been implicated in suppressing apoptosis, and it was hypothesized that they would increase the number of GSC/BTIC-like cells grown in vitro and improve cloning efficiencies. Indeed, our data demonstrate that transient and continuous supplementation of non-toxic concentrations of Y-27632 and fasudil inhibited apoptosis, enhanced the cells' ability to form spheres, and increased stem cell marker expressing GSC/BTIC-like cell subpopulation. Our data indicated that pharmacological and genetic (siRNA) inhibitions of the ROCK pathway facilitates in vitro expansion of GSC/BTIC-like cells. Thus, ROCK pathway inhibition shows promise for future optimization of CSC culture media.

Indexed as

ApoptosisBrain NeoplasmsCell Line, TumorGlioblastomaHumansIn Vitro TechniquesNeoplastic Stem CellsProtein Kinase Inhibitorsrho-Associated KinasesProtein Kinase Inhibitorsrho-Associated Kinases

Identifiers

PMID26167936
PMCPMC4500389
OpenAlexW933087622

What OpenQuestion holds

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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 OpenQuestion graph.