Evidence map›Paper›PMID 29927251›Full record

ArticleNano letters2018

Bioreducible Polymeric Nanoparticles Containing Multiplexed Cancer Stem Cell Regulating miRNAs Inhibit Glioblastoma Growth and Prolong Survival.

Hernando Lopez-Bertoni, Kristen L Kozielski, Yuan Rui, Bachchu Lal, Hannah Vaughan, David R Wilson, Nicole Mihelson, Charles G Eberhart, John Laterra, Jordan J Green

Abstract read
In one paragraph

Article in Nano letters, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed, 1 pooled it
–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

80 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  18. Emerging Perspectives on Prime Editor Delivery to the Brain.Pharmaceuticals (Basel, Switzerland) · 2024
    Review
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20 more citing papers are in PubMed but not listed here.

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

10 authors.

Hernando Lopez-BertoniHugo W. Moser Research Institute at Kennedy Krieger , Baltimore , Maryland 21205 , United States.
Kristen L KozielskiDepartment of Biomedical Engineering , Institute for NanoBioTechnology, and the Translational Tissue Engineering Center, Johns Hopkins University School of Medicine , Baltimore , Maryland 21231 , United States.
Yuan RuiDepartment of Biomedical Engineering , Institute for NanoBioTechnology, and the Translational Tissue Engineering Center, Johns Hopkins University School of Medicine , Baltimore , Maryland 21231 , United States.
Bachchu LalHugo W. Moser Research Institute at Kennedy Krieger , Baltimore , Maryland 21205 , United States.
Hannah VaughanDepartment of Biomedical Engineering , Institute for NanoBioTechnology, and the Translational Tissue Engineering Center, Johns Hopkins University School of Medicine , Baltimore , Maryland 21231 , United States.
David R WilsonDepartment of Biomedical Engineering , Institute for NanoBioTechnology, and the Translational Tissue Engineering Center, Johns Hopkins University School of Medicine , Baltimore , Maryland 21231 , United States.
Nicole MihelsonHugo W. Moser Research Institute at Kennedy Krieger , Baltimore , Maryland 21205 , United States.
Charles G Eberhart
John LaterraHugo W. Moser Research Institute at Kennedy Krieger , Baltimore , Maryland 21205 , United States.
Jordan J GreenDepartment of Biomedical Engineering , Institute for NanoBioTechnology, and the Translational Tissue Engineering Center, Johns Hopkins University School of Medicine , Baltimore , Maryland 21231 , United States.ORCID 0000-0003-4176-3808

Funding

Sleep and Circadian Dysfunction, Brain and Neurobehavioral Development in AutismP50HD103538 · NICHD · HUGO W. MOSER RES INST KENNEDY KRIEGER · PI Stewart H Mostofsky · 2020 to 2026
$9.9M
Chromatin Modifications in GBM-Propagating CellsR01NS096754 · NINDS · HUGO W. MOSER RES INST KENNEDY KRIEGER · PI LATERRA, JOHN J · 2017 to 2021
$2.2M
Gene Delivery Nanoparticles to Treat GlioblastomaR01EB016721 · NIBIB · JOHNS HOPKINS UNIVERSITY · PI GREEN, JORDAN · 2013 to 2017
$1.9M
Nanoparticle Modified Human Fat Derived Mesenchymal Stem Cells for Brain Cancer (Change of Organization Application)R01CA195503 · NCI · MAYO CLINIC JACKSONVILLE · PI GREEN, JORDAN, QUINONES-HINOJOSA, ALFREDO · 2016 to 2020
$1.9M
Brain Cancer Stem Cell Reprogramming by c-MetR01NS073611 · NINDS · HUGO W. MOSER RES INST KENNEDY KRIEGER · PI LATERRA, JOHN J · 2012 to 2016
$1.8M
Zeiss LSM780 Confocal Microscope for a Core FacilityS10OD016374 · OD · JOHNS HOPKINS UNIVERSITY · PI KUO, SCOT CHARLES · 2013 to 2013
$584k
Nanoparticles for selective and combinatorial delivery of siRNA to brain cancerF31CA196163 · NCI · JOHNS HOPKINS UNIVERSITY · PI KOZIELSKI, KRISTEN LYNN · 2015 to 2016
$68k
NCI NIH HHS F31 CA196163NCI NIH HHS R01 CA195503NIBIB NIH HHS R01 EB016721NICHD NIH HHS P50 HD103538NIH HHS S10 OD016374NINDS NIH HHS R01 NS073611NINDS NIH HHS R01 NS096754
6 · The paper itself

Abstract

Despite our growing molecular-level understanding of glioblastoma (GBM), treatment modalities remain limited. Recent developments in the mechanisms of cell fate regulation and nanomedicine provide new avenues by which to treat and manage brain tumors via the delivery of molecular therapeutics. Here, we have developed bioreducible poly(β-amino ester) nanoparticles that demonstrate high intracellular delivery efficacy, low cytotoxicity, escape from endosomes, and promotion of cytosol-targeted environmentally triggered cargo release for miRNA delivery to tumor-propagating human cancer stem cells. In this report, we combined this nanobiotechnology with newly discovered cancer stem cell inhibiting miRNAs to develop self-assembled miRNA-containing polymeric nanoparticles (nano-miRs) to treat gliomas. We show that these nano-miRs effectively intracellularly deliver single and combination miRNA mimics that inhibit the stem cell phenotype of human GBM cells in vitro. Following direct intratumoral infusion, these nano-miRs were found to distribute through the tumors, inhibit the growth of established orthotopic human GBM xenografts, and cooperatively enhance the response to standard-of-care γ radiation. Co-delivery of two miRNAs, miR-148a and miR-296-5p, within the bioreducible nano-miR particles enabled long-term survival from GBM in mice.

Indexed as

AnimalsCell Line, TumorCell ProliferationCell SurvivalGlioblastomaHumansMiceMicroRNAsNanomedicineNanoparticlesNeoplastic Stem CellsPolymersMicroRNAsPolymersbioreduciblebrain cancercancer stem cellmiRNAnanomedicinepolymer

Identifiers

PMID29927251
PMCPMC6197883

What OpenQuestion holds

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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.