Evidence map›Paper›PMID 26203676›Full record

ArticleACS nano2015

Spatiotemporal Targeting of a Dual-Ligand Nanoparticle to Cancer Metastasis.

Elizabeth Doolittle, Pubudu M Peiris, Gilad Doron, Amy Goldberg, Samantha Tucci, Swetha Rao, Shruti Shah, Meilyn Sylvestre, Priya Govender, Oguz Turan and 3 more

Abstract read
In one paragraph

Article in ACS nano, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing 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

42 citing papers in PubMed.

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  17. Biomedical nanoparticle design: What we can learn from viruses.Journal of controlled release : official journal of the Controlled Release Society · 2021
    Review
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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

13 authors.

Elizabeth DoolittleDepartment of Biomedical Engineering, ‡Department of Radiology, §Case Center for Imaging Research, and ∥Case Comprehensive Cancer Center, Case Western Reserve University , Cleveland 44106, Ohio, United States.
Pubudu M PeirisDepartment of Biomedical Engineering, ‡Department of Radiology, §Case Center for Imaging Research, and ∥Case Comprehensive Cancer Center, Case Western Reserve University , Cleveland 44106, Ohio, United States.
Gilad DoronDepartment of Biomedical Engineering, ‡Department of Radiology, §Case Center for Imaging Research, and ∥Case Comprehensive Cancer Center, Case Western Reserve University , Cleveland 44106, Ohio, United States.
Amy GoldbergDepartment of Biomedical Engineering, ‡Department of Radiology, §Case Center for Imaging Research, and ∥Case Comprehensive Cancer Center, Case Western Reserve University , Cleveland 44106, Ohio, United States.
Samantha TucciDepartment of Biomedical Engineering, ‡Department of Radiology, §Case Center for Imaging Research, and ∥Case Comprehensive Cancer Center, Case Western Reserve University , Cleveland 44106, Ohio, United States.
Swetha RaoDepartment of Biomedical Engineering, ‡Department of Radiology, §Case Center for Imaging Research, and ∥Case Comprehensive Cancer Center, Case Western Reserve University , Cleveland 44106, Ohio, United States.
Shruti ShahDepartment of Biomedical Engineering, ‡Department of Radiology, §Case Center for Imaging Research, and ∥Case Comprehensive Cancer Center, Case Western Reserve University , Cleveland 44106, Ohio, United States.
Meilyn SylvestreDepartment of Biomedical Engineering, ‡Department of Radiology, §Case Center for Imaging Research, and ∥Case Comprehensive Cancer Center, Case Western Reserve University , Cleveland 44106, Ohio, United States.
Priya GovenderDepartment of Biomedical Engineering, ‡Department of Radiology, §Case Center for Imaging Research, and ∥Case Comprehensive Cancer Center, Case Western Reserve University , Cleveland 44106, Ohio, United States.
Oguz TuranDepartment of Biomedical Engineering, ‡Department of Radiology, §Case Center for Imaging Research, and ∥Case Comprehensive Cancer Center, Case Western Reserve University , Cleveland 44106, Ohio, United States.
Zhenghong LeeDepartment of Biomedical Engineering, ‡Department of Radiology, §Case Center for Imaging Research, and ∥Case Comprehensive Cancer Center, Case Western Reserve University , Cleveland 44106, Ohio, United States.
William P SchiemannDepartment of Biomedical Engineering, ‡Department of Radiology, §Case Center for Imaging Research, and ∥Case Comprehensive Cancer Center, Case Western Reserve University , Cleveland 44106, Ohio, United States.
Efstathios KarathanasisDepartment of Biomedical Engineering, ‡Department of Radiology, §Case Center for Imaging Research, and ∥Case Comprehensive Cancer Center, Case Western Reserve University , Cleveland 44106, Ohio, United States.

Funding

Clinical and Translational Science Collaborative of ClevelandUL1TR000439 · NCATS · CASE WESTERN RESERVE UNIVERSITY · PI KONSTAN, MICHAEL W. · 2012 to 2016
$50.0M
Interdisciplinary Biomedical Imaging Training ProgramT32EB007509 · NIBIB · CASE WESTERN RESERVE UNIVERSITY · PI DAVID Lynn WILSON, Xin Yu · 2007 to 2026
$5.6M
Predoctoral Training in Pharmacological SciencesT32GM099608 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI HELL, JOHANNES W · 2012 to 2021
$2.2M
Detection of micrometastasis using a dual-ligand nanoparticleR01CA177716 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI KARATHANASIS, EFSTATHIOS · 2013 to 2017
$1.6M
NCATS NIH HHS UL1 TR000439NCI NIH HHS R01 CA177716NCI NIH HHS R01CA177716NIBIB NIH HHS T32 EB007509NIBIB NIH HHS T32EB007509NIGMS NIH HHS T32 GM099608
6 · The paper itself

Abstract

Various targeting strategies and ligands have been employed to direct nanoparticles to tumors that upregulate specific cell-surface molecules. However, tumors display a dynamic, heterogeneous microenvironment, which undergoes spatiotemporal changes including the expression of targetable cell-surface biomarkers. Here, we investigated a dual-ligand nanoparticle to effectively target two receptors overexpressed in aggressive tumors. By using two different chemical specificities, the dual-ligand strategy considered the spatiotemporal alterations in the expression patterns of the receptors in cancer sites. As a case study, we used two mouse models of metastasis of triple-negative breast cancer using the MDA-MB-231 and 4T1 cells. The dual-ligand system utilized two peptides targeting P-selectin and αvβ3 integrin, which are functionally linked to different stages of the development of metastatic disease at a distal site. Using in vivo multimodal imaging and post mortem histological analyses, this study shows that the dual-ligand nanoparticle effectively targeted metastatic disease that was otherwise missed by single-ligand strategies. The dual-ligand nanoparticle was capable of capturing different metastatic sites within the same animal that overexpressed either receptor or both of them. Furthermore, the highly efficient targeting resulted in 22% of the injected dual-ligand nanoparticles being deposited in early-stage metastases within 2 h after injection.

Indexed as

1,2-DipalmitoylphosphatidylcholineAnimalsCell Line, TumorCholesterolDiagnostic ImagingDrug CompoundingDrug Delivery SystemsFemaleGene ExpressionHumansIntegrin alphaVbeta3Lung NeoplasmsMiceMice, Inbred BALB CNanoparticlesNeoplasm Transplantation1,2-DipalmitoylphosphatidylcholineCholesterolIntegrin alphaVbeta3P-SelectinRecombinant Proteinscancer metastasisdual-ligand nanoparticletriple-negative breast cancervascular targeting

Identifiers

PMID26203676
PMCPMC4579532

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.