Evidence map›Paper›PMID 39248512›Full record

ArticleJournal of visualized experiments : JoVE2024

Monitoring of Nanodrug Accumulation in Murine Breast Cancer Metastases.

Alan Halim, Sujan Kumar Mondal, Nasreen Al-Qadi, Elizabeth Kenyon, Keith MacRenaris, Thomas V O'Halloran, Zdravka Medarova, Anna Moore

Abstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–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

2 citing papers in PubMed.

  1. Article
  2. 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

8 authors.

Alan HalimPrecision Health Program, Michigan State University.
Sujan Kumar MondalPrecision Health Program, Michigan State University; Department of Radiology, College of Human Medicine, Michigan State University.
Nasreen Al-QadiPrecision Health Program, Michigan State University.
Elizabeth KenyonPrecision Health Program, Michigan State University; Department of Radiology, College of Human Medicine, Michigan State University.
Keith MacRenarisDepartment of Microbiology, Genetics, & Immunology, College of Natural Science, Michigan State University; Elemental Health Institute, Michigan State University.
Thomas V O'HalloranDepartment of Chemistry, College of Natural Science, Michigan State University; Elemental Health Institute, Michigan State University.
Zdravka MedarovaTranscode Therapeutics Inc.
Anna MoorePrecision Health Program, Michigan State University; Department of Radiology, College of Human Medicine, Michigan State University; moorea57@msu.edu.

Funding

TR&D Project 3: Photoacoustic Detection of Metal Fluxes at the Tissue LevelP41GM135018 · NIGMS · NORTHWESTERN UNIVERSITY · PI MACRENARIS, KEITH W · 2020 to 2024
$5.8M
Therapy for Metastatic breast cancer based on micro RNA silencingR01CA221771 · NCI · MICHIGAN STATE UNIVERSITY · PI MOORE, ANNA · 2018 to 2022
$2.9M
Regulatory Roles of Zinc Fluxes in Metalloprotein Occupancy and Cell Cycle ProgressionR01GM115848 · NIGMS · NORTHWESTERN UNIVERSITY · PI O'HALLORAN, THOMAS V · 2015 to 2025
$2.8M
NCI NIH HHS R01 CA221771NIGMS NIH HHS P41 GM135018NIGMS NIH HHS R01 GM115848
6 · The paper itself

Abstract

Metastatic breast cancer is a devastating disease with very limited therapeutic options, calling for new therapeutic strategies. Oncogenic miRNAs have been shown to be associated with the metastatic potential of breast cancer and are implicated in tumor cell migration, invasion, and viability. However, it can be difficult to deliver an inhibitory RNA molecule to the tissue of interest. To overcome this challenge and deliver active antisense oligonucleotides to tumors, we utilized magnetic iron oxide nanoparticles as a delivery platform. These nanoparticles target tissues with increased vascular permeability, such as sites of inflammation or cancer. Delivery of these nanoparticles can be monitored in vivo by magnetic resonance imaging (MRI) due to their magnetic properties. Translation of this therapeutic approach into the clinic will be more accessible because of its compatibility with this relevant imaging modality. They can also be labeled with other imaging reporters such as a Cy5.5 near-infrared optical dye for correlative optical imaging and fluorescence microscopy. Here, we demonstrate that nanoparticles labeled with Cy5.5 and conjugated to therapeutic oligomers targeting oncogenic miRNA-10b (termed MN-anti-miR10b, or "nanodrug") administered intravenously accumulate in metastatic sites, opening a possibility for therapeutic intervention of metastatic breast cancer.

Indexed as

CarbocyaninesMicroRNAsAnimalsBreast NeoplasmsFemaleMagnetic Iron Oxide NanoparticlesMagnetic Resonance ImagingMammary Neoplasms, ExperimentalMiceOligonucleotides, AntisenseCarbocyaninesCY5.5 cyanine dyeMicroRNAsOligonucleotides, Antisense

Identifiers

PMID39248512
PMCPMC12920022

What OpenQuestion holds

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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.