Evidence map›Paper›PMID 28783169›Full record

ArticleOncogene2017

Glioblastoma stem cells exploit the αvβ8 integrin-TGFβ1 signaling axis to drive tumor initiation and progression.

P A Guerrero, J H Tchaicha, Z Chen, J E Morales, N McCarty, Q Wang, E P Sulman, G Fuller, F F Lang, G Rao and 1 more

Abstract read
In one paragraph

Article in Oncogene, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

37 citing papers in PubMed, 71 citations in OpenAlex.

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  11. Dichotomous transactivation domains contribute to growth inhibitory and promotion functions of TAp73.Proceedings of the National Academy of Sciences of the United States of America · 2024
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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 at 2 institutions in 1 country.

P A GuerreroDepartment of Neurosurgery, M. D. Anderson Cancer Center, Houston, TX, USA.
J H TchaichaDepartment of Neurosurgery, M. D. Anderson Cancer Center, Houston, TX, USA.
Z ChenDepartment of Neurosurgery, M. D. Anderson Cancer Center, Houston, TX, USA.
J E MoralesDepartment of Neurosurgery, M. D. Anderson Cancer Center, Houston, TX, USA.
N McCartyThe Brown Institute for Molecular Medicine, University of Texas Health Science Center at Houston, Houston, TX, USA.
Q WangDepartment of Radiation Oncology, M. D. Anderson Cancer Center, Houston, TX, USA.
E P SulmanDepartment of Radiation Oncology, M. D. Anderson Cancer Center, Houston, TX, USA.
G FullerDepartments of Pathology, M. D. Anderson Cancer Center, Houston, TX, USA.
F F LangDepartment of Neurosurgery, M. D. Anderson Cancer Center, Houston, TX, USA.
G RaoDepartment of Neurosurgery, M. D. Anderson Cancer Center, Houston, TX, USA.
J H McCartyDepartment of Neurosurgery, M. D. Anderson Cancer Center, Houston, TX, USA.
The University of Texas MD Anderson Cancer Center · USInstitute for Molecular Medicine · US

Funding

Tropism Enhanced Oncolytic Adenovirus for the Treatment of Brain TumorsP50CA127001 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Juan Fueyo · 2008 to 2026
$41.2M
Signal Transduction by alphaVbeta8 IntegrinR01NS087635 · NINDS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI MCCARTY, JOSEPH H · 2014 to 2024
$3.7M
Deciphering mechanisms of perivascular tumor cell invasion in glioblastomaR01NS078402 · NINDS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI MCCARTY, JOSEPH H · 2012 to 2016
$1.9M
MODELING MALIGNANT PROGRESSION IN GLIOMAR01NS094615 · NINDS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI RAO, GANESH · 2016 to 2020
$1.8M
NCI NIH HHS P50 CA127001NINDS NIH HHS R01 NS078402NINDS NIH HHS R01 NS087635NINDS NIH HHS R01 NS094615
6 · The paper itself

Abstract

Glioblastoma (GBM) is a primary brain cancer that contains populations of stem-like cancer cells (GSCs) that home to specialized perivascular niches. GSC interactions with their niche influence self-renewal, differentiation and drug resistance, although the pathways underlying these events remain largely unknown. Here, we report that the integrin αvβ8 and its latent transforming growth factor β1 (TGFβ1) protein ligand have central roles in promoting niche co-option and GBM initiation. αvβ8 integrin is highly expressed in GSCs and is essential for self-renewal and lineage commitment in vitro. Fractionation of β8

Indexed as

AC133 AntigenAnimalsBiomarkers, TumorBrain NeoplasmsCarcinogenesisCell DifferentiationCell Line, TumorCell Self RenewalDisease ProgressionGlioblastomaHumansIntegrin beta ChainsIntegrinsMiceMice, SCIDM Phase Cell Cycle CheckpointsAC133 AntigenBiomarkers, Tumorintegrin alphavbeta8integrin beta8Integrin beta ChainsIntegrinsSOXB1 Transcription FactorsTransforming Growth Factor beta1

Identifiers

PMID28783169
PMCPMC5882487
OpenAlexW2744758704

What OpenQuestion holds

Textmetadata
LicenceTDM
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.