Evidence map›Paper›PMID 37351172›Full record

ArticleTheranostics2023

Non-viral nitric oxide-based gene therapy improves perfusion and liposomal doxorubicin sonopermeation in neuroblastoma models.

Aditi Bellary, Chance Nowak, Isabella Iwanicki, Fernando Flores-Guzman, Lydia Wu, Jessica J Kandel, Theodore W Laetsch, Leonidas Bleris, Sonia L Hernandez, Shashank R Sirsi

Open access · goldAbstract read
In one paragraph

Article in Theranostics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

14 citing papers in PubMed, 14 citations in OpenAlex.

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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

10 authors at 3 institutions in 1 country.

Aditi BellaryDepartment of Biomedical Engineering, University of Texas at Dallas, Richardson, TX, USA.
Chance NowakDepartment of Biological Sciences, University of Texas at Dallas, Richardson, TX, USA.
Isabella IwanickiDepartment of Surgery, University of Chicago Medical School, Chicago, IL, USA.
Fernando Flores-GuzmanDepartment of Surgery, University of Chicago Medical School, Chicago, IL, USA.
Lydia WuDepartment of Surgery, University of Chicago Medical School, Chicago, IL, USA.
Jessica J KandelDepartment of Surgery, University of Chicago Medical School, Chicago, IL, USA.
Theodore W LaetschDivision of Oncology and Center for Childhood Cancer Research, Children's Hospital of Philadelphia and the Department of Pediatrics and Abramson Cancer Center, University of Pennsylvania, Philadelphia, PA, USA.
Leonidas BlerisDepartment of Biomedical Engineering, University of Texas at Dallas, Richardson, TX, USA.
Sonia L HernandezDepartment of Surgery, University of Chicago Medical School, Chicago, IL, USA.
Shashank R SirsiDepartment of Biomedical Engineering, University of Texas at Dallas, Richardson, TX, USA.
Rosalind Franklin University of Medicine and Science · USThe University of Texas at Dallas · USChildren's Hospital of Philadelphia · US

Funding

VIRAL ONCOLOGY CORE FACILITYP30CA014599 · NCI · UNIVERSITY OF CHICAGO · PI MARK W. LINGEN · 1985 to 2026
$122.1M
Development of Novel Acoustic Clusters for Improving Combinatorial Neuroblastoma TherapyR01CA235756 · NCI · UNIVERSITY OF TEXAS DALLAS · PI HERNANDEZ, SONIA LORENA, SIRSI, SHASHANK RAMESH · 2019 to 2023
$2.0M
Quantitative Monitoring and Control of Tumor Vascular Permeability in vivo UsingR21EB015040 · NIBIB · UNIVERSITY OF COLORADO · PI BORDEN, MARK ANDREW, KANDEL, JESSICA J · 2012 to 2013
$418k
NCI NIH HHS P30 CA014599NCI NIH HHS R01 CA235756NIBIB NIH HHS R21 EB015040
6 · The paper itself

Abstract

Neuroblastoma (NB) is a pediatric malignancy that accounts for 15% of cancer-related childhood mortality. High-risk NB requires an aggressive chemoradiotherapy regimen that causes significant off-target toxicity. Despite this invasive treatment, many patients either relapse or do not respond adequately. Recent studies suggest that improving tumor perfusion can enhance drug accumulation and distribution within the tumor tissue, potentially augmenting treatment effects without inflicting systemic toxicity. Accordingly, methods that transiently increase tumor perfusion prior to treatment may help combat this disease. Here, we show the use of gene therapy to confer inducible nitric oxide synthase (iNOS) expression solely in the tumor space, using focused ultrasound targeting. NOS catalyzes the reaction that generates nitric oxide (NO), a potent endogenous vasodilator. This study reports the development of a targeted non-viral image-guided platform to deliver iNOS-expressing plasmid DNA (pDNA) to vascular endothelial cells encasing tumor blood vessels. Following transfection, longitudinal quantitative contrast-enhanced ultrasound (qCEUS) imaging revealed an increase in tumor perfusion over 72 h, attributed to elevated intratumoral iNOS expression.

Indexed as

NeuroblastomaNitric OxideChildDNADoxorubicinEndothelial CellsGenetic TherapyHumansNitric Oxide Synthase Type IIPerfusionPolyethylene GlycolsDNADoxorubicinliposomal doxorubicinNitric OxideNitric Oxide Synthase Type IIPolyethylene Glycolsand quantitative contrast-enhanced ultrasound (qCEUS)gene therapyinducible nitric oxide synthase (iNOS)neuroblastomasonopermeation

Identifiers

PMID37351172
PMCPMC10283050
OpenAlexW4380685915

What OpenQuestion holds

Textmetadata
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.