Evidence map›Paper›PMID 24098639›Full record

ArticlePloS one2013

New potential therapeutic approach for the treatment of B-Cell malignancies using chlorambucil/hydroxychloroquine-loaded anti-CD20 nanoparticles.

Nelly Mezzaroba, Sonia Zorzet, Erika Secco, Stefania Biffi, Claudio Tripodo, Marco Calvaruso, Ramiro Mendoza-Maldonado, Sara Capolla, Marilena Granzotto, Ruben Spretz and 11 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

24 citing papers in PubMed, 57 citations in OpenAlex.

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  20. Polymeric chloroquine as an inhibitor of cancer cell migration and experimental lung metastasis.Journal of controlled release : official journal of the Controlled Release Society · 2016
    Article
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

21 authors at 9 institutions in 3 countries.

Nelly MezzarobaDept. of Life Sciences, University of Trieste, Trieste, Italy.
Sonia Zorzet
Erika Secco
Stefania Biffi
Claudio Tripodo
Marco Calvaruso
Ramiro Mendoza-Maldonado
Sara Capolla
Marilena Granzotto
Ruben Spretz
Gustavo Larsen
Sandra Noriega
Marianna Lucafò
Eduardo Mansilla
Chiara Garrovo
Gustavo H Marín
Gabriele Baj
Valter Gattei
Gabriele Pozzato
Luis Núñez
Paolo Macor
University of Trieste · ITIRCCS Materno Infantile Burlo Garofolo · ITLNKChemsolutions · USMinisterio de Salud - Provincia de Buenos Aires · ARTarget (United States) · USUniversity of Palermo · ITCentro di Riferimento Oncologico · ITCluster in Biomedicine · ITInternational Centre for Genetic Engineering and Biotechnology · IT

Funding

Nanoparticles and Nanocapsules for Glioma TargetingR44CA135906 · NCI · LNKCHEMSOLUTIONS · PI NUNEZ, LUIS NUNEZ, SPRETZ, RUBEN · 2011 to 2013
$2.0M
NCI NIH HHS 2R44CA135906-02NCI NIH HHS R44 CA135906
6 · The paper itself

Abstract

Current B-cell disorder treatments take advantage of dose-intensive chemotherapy regimens and immunotherapy via use of monoclonal antibodies. Unfortunately, they may lead to insufficient tumor distribution of therapeutic agents, and often cause adverse effects on patients. In this contribution, we propose a novel therapeutic approach in which relatively high doses of Hydroxychloroquine and Chlorambucil were loaded into biodegradable nanoparticles coated with an anti-CD20 antibody. We demonstrate their ability to effectively target and internalize in tumor B-cells. Moreover, these nanoparticles were able to kill not only p53 mutated/deleted lymphoma cell lines expressing a low amount of CD20, but also circulating primary cells purified from chronic lymphocitic leukemia patients. Their safety was demonstrated in healthy mice, and their therapeutic effects in a new model of Burkitt's lymphoma. The latter serves as a prototype of an aggressive lympho-proliferative disease. In vitro and in vivo data showed the ability of anti-CD20 nanoparticles loaded with Hydroxychloroquine and Chlorambucil to increase tumor cell killing in comparison to free cytotoxic agents or Rituximab. These results shed light on the potential of anti-CD20 nanoparticles carrying Hydroxychloroquine and Chlorambucil for controlling a disseminated model of aggressive lymphoma, and lend credence to the idea of adopting this therapeutic approach for the treatment of B-cell disorders.

Indexed as

Disease Models, AnimalAnimalsAntibodies, Monoclonal, Murine-DerivedAntigens, CD20ApoptosisAutophagyCell SurvivalChlorambucilDrug CombinationsDrug Delivery SystemsFemaleFlow CytometryHydroxychloroquineImmunohistochemistryLymphoma, B-CellMiceAntibodies, Monoclonal, Murine-DerivedAntigens, CD20ChlorambucilDrug CombinationsHydroxychloroquineRituximab

Identifiers

PMID24098639
PMCPMC3787049
OpenAlexW2053124055

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.