Evidence map›Paper›PMID 32121130›Full record

ArticleMolecules (Basel, Switzerland)2020

A New NT4 Peptide-Based Drug Delivery System for Cancer Treatment.

Jlenia Brunetti, Sara Piantini, Marco Fragai, Silvia Scali, Giulia Cipriani, Lorenzo Depau, Alessandro Pini, Chiara Falciani, Stefano Menichetti, Luisa Bracci

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.4field-weighted citation impact, top 16% 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

11 citing papers in PubMed, 21 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.

Jlenia BrunettiDepartment of Medical Biotechnology, University of Siena, via Aldo Moro 2, 53100 Siena, Italy.ORCID 0000-0001-8144-7186
Sara PiantiniDepartment of Chemistry "Ugo Schiff", University of Florence, Via Della Lastruccia 3-13, 50019 Sesto Fiorentino (FI), Italy.
Marco FragaiMagnetic Resonance Center (CERM), via Luigi Sacconi 6, 50019 Sesto Fiorentino (FI), Italy.
Silvia ScaliDepartment of Medical Biotechnology, University of Siena, via Aldo Moro 2, 53100 Siena, Italy.
Giulia CiprianiDepartment of Chemistry "Ugo Schiff", University of Florence, Via Della Lastruccia 3-13, 50019 Sesto Fiorentino (FI), Italy.
Lorenzo DepauDepartment of Medical Biotechnology, University of Siena, via Aldo Moro 2, 53100 Siena, Italy.
Alessandro PiniDepartment of Medical Biotechnology, University of Siena, via Aldo Moro 2, 53100 Siena, Italy.
Chiara FalcianiDepartment of Medical Biotechnology, University of Siena, via Aldo Moro 2, 53100 Siena, Italy.
Stefano MenichettiDepartment of Chemistry "Ugo Schiff", University of Florence, Via Della Lastruccia 3-13, 50019 Sesto Fiorentino (FI), Italy.ORCID 0000-0001-6745-7484
Luisa BracciDepartment of Medical Biotechnology, University of Siena, via Aldo Moro 2, 53100 Siena, Italy.
University of Siena · ITUniversity of Florence · ITInteruniversity Consortium for Magnetic Resonance · IT

Funding

Associazione Italiana per la Ricerca sul Cancro IG 2014 Id. 15564
6 · The paper itself

Abstract

The development of selective tumor targeting agents to deliver multiple units of chemotherapy drugs to cancer tissue would improve treatment efficacy and greatly advance progress in cancer therapy. Here we report a new drug delivery system based on a tetrabranched peptide known as NT4, which is a promising cancer theranostic by virtue of its high cancer selectivity. We developed NT4 directly conjugated with one, two, or three units of paclitaxel and an NT4-based nanosystem, using NIR-emitting quantum dots, loaded with the NT4 tumor-targeting agent and conjugated with paclitaxel, to obtain a NT4-QD-PTX nanodevice designed to simultaneously detect and kill tumor cells. The selective binding and in vitro cytotoxicity of NT4-QD-PTX were higher than for unlabeled QD-PTX when tested on the human colon adenocarcinoma cell line HT-29. NT4-QD-PTX tumor-targeted nanoparticles can be considered promising for early tumor detection and for the development of effective treatments combining simultaneous therapy and diagnosis.

Indexed as

Drug Delivery SystemsPaclitaxelPeptidesQuantum DotsAdenocarcinomaColonic NeoplasmsHT29 CellsHumansPaclitaxelPeptidesdrug deliverypaclitaxelselective tumor-targeting agenttheranostic nanodevices

Identifiers

PMID32121130
PMCPMC7179244
OpenAlexW3009929472

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.