Evidence map›Paper›PMID 38532439›Full record

ArticleJournal of experimental & clinical cancer research : CR2024

Bispecific aptamer-decorated and light-triggered nanoparticles targeting tumor and stromal cells in breast cancer derived organoids: implications for precision phototherapies.

Simona Camorani, Alessandra Caliendo, Elena Morrone, Lisa Agnello, Matteo Martini, Monica Cantile, Margherita Cerrone, Antonella Zannetti, Massimo La Deda, Monica Fedele and 2 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.1field-weighted citation impact, top 5% 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, 22 citations in OpenAlex.

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  11. Harnessing Organoid Platforms for Nanoparticle Drug Development.Drug design, development and therapy · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 7 institutions in 2 countries.

Simona CamoraniInstitute of Experimental Endocrinology and Oncology "Gaetano Salvatore", National Research Council, 80131, Naples, Italy.
Alessandra CaliendoInstitute of Experimental Endocrinology and Oncology "Gaetano Salvatore", National Research Council, 80131, Naples, Italy.
Elena MorroneCNR-NANOTEC Institute of Nanotechnology, National Research Council, Rende, CS, Italy.
Lisa AgnelloInstitute of Experimental Endocrinology and Oncology "Gaetano Salvatore", National Research Council, 80131, Naples, Italy.
Matteo MartiniInstitute of Light and Matter, UMR 5306, Claude Bernard University Lyon 1, Villeurbanne, France.
Monica CantileInstitutional Biobank-Scientific Directorate, National Cancer Institute INT-IRCCS Fondazione G. Pascale, 80131, Naples, Italy.
Margherita CerronePathology Unit, National Cancer Institute INT-IRCCS Fondazione G. Pascale, 80131, Naples, Italy.
Antonella ZannettiInstitute of Biostructures and Bioimaging, National Research Council, 80145, Naples, Italy.
Massimo La DedaCNR-NANOTEC Institute of Nanotechnology, National Research Council, Rende, CS, Italy.
Monica FedeleInstitute of Experimental Endocrinology and Oncology "Gaetano Salvatore", National Research Council, 80131, Naples, Italy.
Loredana RicciardiCNR-NANOTEC Institute of Nanotechnology, National Research Council, Rende, CS, Italy. loredana.ricciardi@cnr.it.
Laura CerchiaInstitute of Experimental Endocrinology and Oncology "Gaetano Salvatore", National Research Council, 80131, Naples, Italy. l.cerchia@ieos.cnr.it.ORCID http://orcid.org/0000-0002-7633-7932
Institute for Experimental Endocrinology and Oncology · ITIstituto Nazionale Tumori IRCCS "Fondazione G. Pascale" · ITUniversity of Salento · ITInstitute of Biostructure and Bioimaging · ITIstituto di Nanotecnologia · ITUniversité Claude Bernard Lyon 1 · FRUniversity of Perugia · IT

Funding

Associazione Italiana per la Ricerca sul Cancro ID. 23052
6 · The paper itself

Abstract

backgroundBased on the established role of cancer-stroma cross-talk in tumor growth, progression and chemoresistance, targeting interactions between tumor cells and their stroma provides new therapeutic approaches. Dual-targeted nanotherapeutics selectively acting on both tumor and stromal cells may overcome the limits of tumor cell-targeting single-ligand nanomedicine due to the complexity of the tumor microenvironment.

methodsGold-core/silica-shell nanoparticles embedding a water-soluble iridium(III) complex as photosensitizer and luminescent probe (Ir

resultsWe show efficient capability of Ir

conclusionsOur study proposes smart, novel and safe multifunctional nanoplatforms simultaneously addressing cancer-stroma within the tumor microenvironment, which are: (i) actively delivered to the targeted cells through highly specific aptamers; (ii) localized by means of their luminescence, and (iii) activated via minimally invasive light, launching efficient tumor death, thus providing innovative precision therapeutics. Given the unique features, the proposed dual targeted nanoformulations may open a new door to precision cancer treatment.

Indexed as

Aptamers, NucleotideNanoparticlesTriple Negative Breast NeoplasmsCell Line, TumorErbB ReceptorsHumansOrganoidsPhototherapyStromal CellsTumor MicroenvironmentAptamers, NucleotideErbB ReceptorsAptamerDual targetingEGFRNanomedicinePatient-derived cancer organoidsPDGFRβPhototherapyTumor microenvironment

Identifiers

PMID38532439
PMCPMC10964525
OpenAlexW4393195769

What Socratic 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 Socratic graph.