Evidence map›Paper›PMID 30537355›Full record

ArticleAdvanced healthcare materials2019

Engineering Controlled Peritumoral Inflammation to Constrain Brain Tumor Growth.

Tarun Saxena, Johnathan G Lyon, S Balakrishna Pai, Daniel Pare, Jessica Amero, Lohitash Karumbaiah, Sheridan L Carroll, Eric Gaupp, Ravi V Bellamkonda

Open access · greenAbstract read
In one paragraph

Article in Advanced healthcare materials, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 38% 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

3 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

9 authors at 5 institutions in 1 country.

Tarun SaxenaDepartment of Biomedical Engineering, Pratt School of Engineering, Duke University, 101 Science Drive, Durham, NC, 27705, USA.
Johnathan G LyonDepartment of Biomedical Engineering, Pratt School of Engineering, Duke University, 101 Science Drive, Durham, NC, 27705, USA.
S Balakrishna PaiWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology & Emory School of Medicine, UA Whitaker Building, 313 Ferst Drive, Atlanta, GA, 30332, USA.
Daniel PareWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology & Emory School of Medicine, UA Whitaker Building, 313 Ferst Drive, Atlanta, GA, 30332, USA.
Jessica AmeroWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology & Emory School of Medicine, UA Whitaker Building, 313 Ferst Drive, Atlanta, GA, 30332, USA.
Lohitash KarumbaiahRegenerative Bioscience Center, The University of Georgia, 425 River Road, ADS Complex, Athens, GA, 30602, USA.
Sheridan L CarrollDepartment of Biomedical Engineering, Pratt School of Engineering, Duke University, 101 Science Drive, Durham, NC, 27705, USA.
Eric GauppWallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology & Emory School of Medicine, UA Whitaker Building, 313 Ferst Drive, Atlanta, GA, 30332, USA.
Ravi V BellamkondaDepartment of Biomedical Engineering, Pratt School of Engineering, Duke University, 101 Science Drive, Durham, NC, 27705, USA.
The Wallace H. Coulter Department of Biomedical Engineering · USDuke University · USPratt Institute · USGeorgia Institute of Technology · USUniversity of Georgia · US

Funding

Instrumentation for Quantitative Phosphoproteomics and AcetylomicsS10OD012266 · OD · DUKE UNIVERSITY · PI MOSELEY, MARTIN ARTHUR · 2014 to 2014
$320k
Ian's Friends FoundationNIH HHS S10 OD012266NIH HHS S10OD012266-01A1
6 · The paper itself

Abstract

Brain tumors remain a great clinical challenge, in part due to their capacity to invade into eloquent, inoperable regions of the brain. In contrast, inflammation in the central nervous system (CNS) due to injuries activates microglia and astrocytes culminating in an astroglial scar that typically "walls-off" the injury site. Here, the hypothesis is tested that targeting peritumoral cells surrounding tumors to activate them via an inflammatory stimulus that recapitulates the sequelae of a traumatic CNS injury, could generate an environment that would wall-off and contain invasive tumors in the brain. Gold nanoparticles coated with inflammatory polypeptides to target stromal cells in close vicinity to glioblastoma (GBM) tumors, in order to activate these cells and stimulate stromal CNS inflammation, are engineered. It is reported that this approach significantly contains tumors in rodent models of GBM relative to control treatments (reduction in tumor volume by over 300% in comparison to controls), by the activation of the innate and adaptive immune response, and by triggering pathways related to cell clustering. Overall, this report outlines an approach to contain invasive tumors that can complement adjuvant interventions for invasive GBM such as radiation and chemotherapy.

Indexed as

Adaptive ImmunityImmunity, InnateAnimalsAstrocytesBrain NeoplasmsCell Line, TumorGlioblastomaHumansInflammationMiceMicrogliaRatsRats, Nudeglial scarsglioblastomainflammationreactive gliosisstromal reprogramming

Identifiers

PMID30537355
PMCPMC6657526
OpenAlexW2903980561

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.