Evidence map›Paper›PMID 23714122›Full record

ArticleJournal of controlled release : official journal of the Controlled Release Society2013

Novel phage display-derived neuroblastoma-targeting peptides potentiate the effect of drug nanocarriers in preclinical settings.

Monica Loi, Daniela Di Paolo, Marco Soster, Chiara Brignole, Alice Bartolini, Laura Emionite, Jessica Sun, Pamela Becherini, Flavio Curnis, Andrea Petretto and 14 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of controlled release : official journal of the Controlled Release Society, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

19 citing papers in PubMed, 44 citations in OpenAlex.

  1. Review
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  11. Ligand-targeted theranostic nanomedicines against cancer.Journal of controlled release : official journal of the Controlled Release Society · 2016
    Review
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  14. Article
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  16. Convergence of nanotechnology and cancer prevention: are we there yet?Cancer prevention research (Philadelphia, Pa.) · 2014
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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

24 authors at 9 institutions in 3 countries.

Monica LoiExperimental Therapy Unit, Laboratory of Oncology, Istituto Giannina Gaslini, Genoa, Italy.
Daniela Di Paolo
Marco Soster
Chiara Brignole
Alice Bartolini
Laura Emionite
Jessica Sun
Pamela Becherini
Flavio Curnis
Andrea Petretto
Monica Sani
Alessandro Gori
Marco Milanese
Claudio Gambini
Renato Longhi
Michele Cilli
Theresa M Allen
Federico Bussolino
Wadih Arap
Renata Pasqualini
Angelo Corti
Mirco Ponzoni
Serena Marchiò
Fabio Pastorino
Istituto Giannina Gaslini · ITCandiolo Cancer Institute · ITInstitute of Chemistry of Molecular Recognition · ITThe University of Texas MD Anderson Cancer Center · USIstituti di Ricovero e Cura a Carattere Scientifico · ITOspedale Policlinico San Martino · ITSan Raffaele University of Rome · ITUniversity of Alberta · CAUniversity of Genoa · IT

Funding

Texas Center for Cancer NanomedicineU54CA151668 · NCI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI FERRARI, MAURO · 2010 to 2014
$12.4M
NCI NIH HHS U54 CA151668
6 · The paper itself

Abstract

Molecular targeting of drug delivery nanocarriers is expected to improve their therapeutic index while decreasing their toxicity. Here we report the identification and characterization of novel peptide ligands specific for cells present in high-risk neuroblastoma (NB), a childhood tumor mostly refractory to current therapies. To isolate such targeting moieties, we performed combined in vitro/ex-vivo phage display screenings on NB cell lines and on tumors derived from orthotopic mouse models of human NB. By designing proper subtractive protocols, we identified phage clones specific either for the primary tumor, its metastases, or for their respective stromal components. Globally, we isolated 121 phage-displayed NB-binding peptides: 26 bound the primary tumor, 15 the metastatic mass, 57 and 23 their respective microenvironments. Of these, five phage clones were further validated for their specific binding ex-vivo to biopsies from stage IV NB patients and to NB tumors derived from mice. All five clones also targeted tumor cells and vasculature in vivo when injected into NB-bearing mice. Coupling of the corresponding targeting peptides with doxorubicin-loaded liposomes led to a significant inhibition in tumor volume and enhanced survival in preclinical NB models, thereby paving the way to their clinical development.

Indexed as

AnimalsCell Line, TumorCells, CulturedCell Surface Display TechniquesCell SurvivalDoxorubicinFemaleHumansHuman Umbilical Vein Endothelial CellsLiposomesMiceMice, NudeNanoparticlesNeuroblastomaPeptidesTumor BurdenDoxorubicinLiposomesPeptidesLiposomesNanocarriersNeuroblastomaPeptidesPhage display screeningTargeted therapy

Identifiers

PMID23714122
PMCPMC4317336
OpenAlexW2160591216

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.