Evidence map›Paper›PMID 33716502›Full record

ArticleInternational journal of nanomedicine2021

Specific Cytotoxic Effect of an Auristatin Nanoconjugate Towards CXCR4

Aïda Falgàs, Victor Pallarès, Ugutz Unzueta, Yáiza Núñez, Jorge Sierra, Alberto Gallardo, Lorena Alba-Castellón, Maria Antonia Mangues, Patricia Álamo, Antonio Villaverde and 3 more

Open access · goldAbstract read
In one paragraph

Article in International journal of nanomedicine, 2021. 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
2.7field-weighted citation impact, top 10% 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, 25 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

13 authors at 2 institutions in 1 country.

Aïda FalgàsBiomedical Research Institute Sant Pau (IIB-Sant Pau), Hospital de la Santa Creu i Sant Pau, Barcelona, 08025, Spain.
Victor PallarèsBiomedical Research Institute Sant Pau (IIB-Sant Pau), Hospital de la Santa Creu i Sant Pau, Barcelona, 08025, Spain.
Ugutz UnzuetaBiomedical Research Institute Sant Pau (IIB-Sant Pau), Hospital de la Santa Creu i Sant Pau, Barcelona, 08025, Spain.
Yáiza NúñezBiomedical Research Institute Sant Pau (IIB-Sant Pau), Hospital de la Santa Creu i Sant Pau, Barcelona, 08025, Spain.
Jorge SierraJosep Carreras Leukaemia Research Institute (IJC), Barcelona, 08916, Spain.
Alberto GallardoBiomedical Research Institute Sant Pau (IIB-Sant Pau), Hospital de la Santa Creu i Sant Pau, Barcelona, 08025, Spain.
Lorena Alba-CastellónBiomedical Research Institute Sant Pau (IIB-Sant Pau), Hospital de la Santa Creu i Sant Pau, Barcelona, 08025, Spain.
Maria Antonia ManguesCIBER de Bioingeniería Biomateriales y Nanomedicina (CIBER-BBN), Madrid, 28029, Spain.ORCID 0000-0002-1438-8515
Patricia ÁlamoBiomedical Research Institute Sant Pau (IIB-Sant Pau), Hospital de la Santa Creu i Sant Pau, Barcelona, 08025, Spain.
Antonio VillaverdeCIBER de Bioingeniería Biomateriales y Nanomedicina (CIBER-BBN), Madrid, 28029, Spain.
Esther VázquezCIBER de Bioingeniería Biomateriales y Nanomedicina (CIBER-BBN), Madrid, 28029, Spain.
Ramon ManguesBiomedical Research Institute Sant Pau (IIB-Sant Pau), Hospital de la Santa Creu i Sant Pau, Barcelona, 08025, Spain.ORCID 0000-0003-2661-9525
Isolda CasanovaBiomedical Research Institute Sant Pau (IIB-Sant Pau), Hospital de la Santa Creu i Sant Pau, Barcelona, 08025, Spain.
Hospital de Sant Pau · ESUniversitat Autònoma de Barcelona · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeAround 40-50% of diffuse large-B cell lymphoma (DLBCL) patients suffer from refractory disease or relapse after R-CHOP first-line treatment. Many ongoing clinical trials for DLBCL patients involve microtubule targeting agents (MTAs), however, their anticancer activity is limited by severe side effects. Therefore, we chose to improve the therapeutic window of the MTA monomethyl auristatin E developing a nanoconjugate, T22-AUR, that selectively targets the CXCR4 receptor, which is overexpressed in many DLBCL cells (CXCR4

methodsThe T22-AUR specificity towards CXCR4 receptor was performed by flow cytometry in different DLBCL cell lines and running biodistribution assays in a subcutaneous mouse model bearing CXCR4

resultsWe demonstrate that the T22-AUR nanoconjugate displays CXCR4-dependent targeting and internalization in CXCR4

conclusionT22-AUR exerts in vitro and in vivo anticancer effect on CXCR4

Indexed as

AnimalsAntineoplastic AgentsCell DeathCell Line, TumorDisease Models, AnimalEndocytosisFemaleHumansLeukocytes, MononuclearLymphoma, Large B-Cell, DiffuseLysosomesMiceMice, Inbred NODMice, SCIDNanoconjugatesOligopeptidesAntineoplastic Agentsmonomethyl auristatin ENanoconjugatesOligopeptidesReceptors, CXCR4DLBCLMMAEnanomedicinetargeted drug delivery

Identifiers

PMID33716502
PMCPMC7944372
OpenAlexW3133812458

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.