Evidence map›Paper›PMID 30604643›Full record

ArticlemAbs2019

A recycling anti-transferrin receptor-1 monoclonal antibody as an efficient therapy for erythroleukemia through target up-regulation and antibody-dependent cytotoxic effector functions.

Madeline Neiveyans, Rana Melhem, Christophe Arnoult, Thomas Bourquard, Marta Jarlier, Muriel Busson, Adrien Laroche, Martine Cerutti, Martine Pugnière, David Ternant and 6 more

Open access · goldAbstract read
In one paragraph

Article in mAbs, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

18 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

16 authors at 5 institutions in 1 country.

Madeline Neiveyansa IRCM, Institut de Recherche en Cancérologie de Montpellier ; INSERM, U1194, Université de Montpellier, Montpellier , France.
Rana Melhema IRCM, Institut de Recherche en Cancérologie de Montpellier ; INSERM, U1194, Université de Montpellier, Montpellier , France.
Christophe Arnoultc CNRS , GICC UMR 7292 , Tours , France.
Thomas Bourquarde UMR INRA CNRS Physiologie de la reproduction et des comportements, Université François Rabelais de Tours , Nouzilly , France.ORCID 0000-0002-9670-711X
Marta Jarlierb ICM , Institut régional du Cancer de Montpellier , Montpellier , France.
Muriel Bussona IRCM, Institut de Recherche en Cancérologie de Montpellier ; INSERM, U1194, Université de Montpellier, Montpellier , France.ORCID 0000-0001-5936-4026
Adrien Larochea IRCM, Institut de Recherche en Cancérologie de Montpellier ; INSERM, U1194, Université de Montpellier, Montpellier , France.
Martine Ceruttif CNRS, UPS3044 Saint-Christol-Lèz-Alès , France.
Martine Pugnièreg PP2I, Plateforme Protéomique et Interactions Moléculaires , IRCM.
David Ternantc CNRS , GICC UMR 7292 , Tours , France.
Nadège Gaborita IRCM, Institut de Recherche en Cancérologie de Montpellier ; INSERM, U1194, Université de Montpellier, Montpellier , France.ORCID 0000-0001-6447-6735
Thierry Chardèsa IRCM, Institut de Recherche en Cancérologie de Montpellier ; INSERM, U1194, Université de Montpellier, Montpellier , France.
Anne Poupone UMR INRA CNRS Physiologie de la reproduction et des comportements, Université François Rabelais de Tours , Nouzilly , France.
Valérie Gouilleux-Gruartc CNRS , GICC UMR 7292 , Tours , France.
Andre Pèlegrina IRCM, Institut de Recherche en Cancérologie de Montpellier ; INSERM, U1194, Université de Montpellier, Montpellier , France.
Marie-Alix Poula IRCM, Institut de Recherche en Cancérologie de Montpellier ; INSERM, U1194, Université de Montpellier, Montpellier , France.ORCID 0000-0001-7157-064X
Inserm · FRUniversité de Tours · FRCentre National de la Recherche Scientifique · FRInstitut de Recherche en Cancérologie de Montpellier · FRPhysique des interactions ioniques et moléculaires · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Targeting transferrin receptor 1 (TfR1) with monoclonal antibodies is a promising therapeutic strategy in cancer as tumor cells often overexpress TfR1 and show increased iron needs. We have re-engineered six anti-human TfR1 single-chain variable fragment (scFv) antibodies into fully human scFv

Indexed as

Antibody-Dependent Cell CytotoxicityAntineoplastic Agents, ImmunologicalLeukemia, Erythroblastic, AcuteSingle-Chain AntibodiesAnimalsAntigens, CDCHO CellsCricetulusHEK293 CellsHumansLymphoma, B-CellMiceMice, KnockoutReceptors, TransferrinAntigens, CDAntineoplastic Agents, ImmunologicalCD71 antigenReceptors, TransferrinSingle-Chain AntibodiesTfrc protein, mouseiron metabolismleukemiatherapeutic antibodyTransferrin receptor 1

Identifiers

PMID30604643
PMCPMC6512944
OpenAlexW2906824906

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.