Evidence map›Paper›PMID 30916923›Full record

ArticleACS nano2019

Radiation-Induced Targeted Nanoparticle-Based Gene Delivery for Brain Tumor Therapy.

Gulsah Erel-Akbaba, Litia A Carvalho, Tian Tian, Max Zinter, Hasan Akbaba, Pierre J Obeid, E Antonio Chiocca, Ralph Weissleder, Ayse Gulten Kantarci, Bakhos A Tannous

Open access · greenAbstract read
In one paragraph

Article in ACS nano, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 90 papers.

0numbers the graph read from it
0cells of the map it votes in
90citing papers in PubMed
9.7field-weighted citation impact, top 1% 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

90 citing papers in PubMed, 199 citations in OpenAlex.

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  10. State-of-the-art application of nanoparticles in radiotherapy: a platform for synergistic effects in cancer treatment.Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] · 2025
    Review
  11. SERPINH1 and CTSZ are Key Markers of Glioma Angiogenesis.Journal of molecular neuroscience : MN · 2025
    Article
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30 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 at 4 institutions in 4 countries.

Gulsah Erel-AkbabaExperimental Therapeutics and Molecular Imaging Lab, Department of Neurology, Neuro-Oncology Division , Massachusetts General Hospital , Charlestown , Massachusetts 02129 , United States.ORCID 0000-0003-3287-5277
Litia A CarvalhoExperimental Therapeutics and Molecular Imaging Lab, Department of Neurology, Neuro-Oncology Division , Massachusetts General Hospital , Charlestown , Massachusetts 02129 , United States.
Tian TianExperimental Therapeutics and Molecular Imaging Lab, Department of Neurology, Neuro-Oncology Division , Massachusetts General Hospital , Charlestown , Massachusetts 02129 , United States.
Max ZinterExperimental Therapeutics and Molecular Imaging Lab, Department of Neurology, Neuro-Oncology Division , Massachusetts General Hospital , Charlestown , Massachusetts 02129 , United States.
Hasan AkbabaExperimental Therapeutics and Molecular Imaging Lab, Department of Neurology, Neuro-Oncology Division , Massachusetts General Hospital , Charlestown , Massachusetts 02129 , United States.
Pierre J ObeidDepartment of Chemistry , University of Balamand , Al Kurah, Deir El-Balamand, P.O. Box 100, Tripoli , Lebanon.
E Antonio ChioccaDepartment of Neurosurgery , Brigham and Women's Hospital , Boston , Massachusetts 02115 , United States.
Ralph WeisslederCenter for Systems Biology, Massachusetts General Hospital , Harvard Medical School , Boston , Massachusetts 02114 , United States.ORCID 0000-0003-0828-4143
Ayse Gulten KantarciDepartment of Pharmaceutical Biotechnology, Faculty of Pharmacy , Ege University , Izmir 35100 , Turkey.
Bakhos A TannousExperimental Therapeutics and Molecular Imaging Lab, Department of Neurology, Neuro-Oncology Division , Massachusetts General Hospital , Charlestown , Massachusetts 02129 , United States.
Harvard University · USBrigham and Women's Hospital · USEge University · TRUniversity of Balamand · LB

Funding

The role of microvesicles in giloma virotherapyP01CA069246 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI CHIOCCA, E. ANTONIO · 1996 to 2021
$30.9M
Interdepartmental Neuroscience CenterP30NS045776 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI BREAKEFIELD, XANDRA OWENS, TANNOUS, BAKHOS A · 2003 to 2018
$11.1M
IVIS Spectrum Imaging SystemS10RR025504 · NCRR · MASSACHUSETTS GENERAL HOSPITAL · PI MOORE, ANNA · 2009 to 2009
$341k
NCI NIH HHS P01 CA069246NCRR NIH HHS S10 RR025504NINDS NIH HHS P30 NS045776
6 · The paper itself

Abstract

Targeted therapy against the programmed cell death ligand-1 (PD-L1) blockade holds considerable promise for the treatment of different tumor types; however, little effect has been observed against gliomas thus far. Effective glioma therapy requires a delivery vehicle that can reach tumor cells in the central nervous system, with limited systemic side effect. In this study, we developed a cyclic peptide iRGD (CCRGDKGPDC)-conjugated solid lipid nanoparticle (SLN) to deliver small interfering RNAs (siRNAs) against both epidermal growth factor receptor (EGFR) and PD-L1 for combined targeted and immunotherapy against glioblastoma, the most aggressive type of brain tumors. Building on recent studies showing that radiation therapy alters tumors for enhanced nanotherapeutic delivery in tumor-associated macrophage-dependent fashion, we showed that low-dose radiation primes targeted SLN uptake into the brain tumor region, leading to enhanced downregulation of PD-L1 and EGFR. Bioluminescence imaging revealed that radiation therapy followed by systemic administration of targeted SLN leads to a significant decrease in glioblastoma growth and prolonged mouse survival. This study combines radiation therapy to prime the tumor for nanoparticle uptake along with the targeting effect of iRGD-conjugated nanoparticles to yield a straightforward but effective approach for combined EGFR inhibition and immunotherapy against glioblastomas, which can be extended to other aggressive tumor types.

Indexed as

Gene Transfer TechniquesRNAi TherapeuticsAnimalsB7-H1 AntigenBrain NeoplasmsErbB ReceptorsFemaleGlioblastomaMice, Inbred C57BLNanomedicineNanoparticlesPeptides, CyclicB7-H1 AntigenCd274 protein, mouseEGFR protein, mouseErbB ReceptorsPeptides, CyclicglioblastomaimmunotherapyPD-L1radiationsolid lipid nanoparticletargeted therapy

Identifiers

PMID30916923
PMCPMC7104714
OpenAlexW2924840189

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.