Evidence map›Paper›PMID 34430714›Full record

ArticleBiochemistry and biophysics reports2021

In vivo monitoring of the therapeutic efficacy of a CXCR1/2 inhibitor with 18F-FDG PET/CT imaging in experimental head and neck carcinoma: A feasibility study.

Christopher Montemagno, Benjamin Serrano, Jérôme Durivault, Valérie Nataf, François Mocquot, Régis Amblard, Valérie Vial, Cyril Ronco, Rachid Benhida, Maeva Dufies and 2 more

Abstract read
In one paragraph

Article in Biochemistry and biophysics reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Thiazole, Isatin and Phthalimide Derivatives TestedCurrent medicinal chemistry · 2024
    Review
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

12 authors.

Christopher MontemagnoDépartement de Biologie Médicale, Centre Scientifique de Monaco, Monaco.
Benjamin SerranoMedical Physics Department, Centre Hospitalier Princesse Grace, Monaco, Monaco.
Jérôme DurivaultDépartement de Biologie Médicale, Centre Scientifique de Monaco, Monaco.
Valérie NatafNuclear Medicine Department, Centre Hospitalier Princesse Grace, Monaco, Monaco.
François MocquotNuclear Medicine Department, Centre Hospitalier Princesse Grace, Monaco, Monaco.
Régis AmblardMedical Physics Department, Centre Hospitalier Princesse Grace, Monaco, Monaco.
Valérie VialDépartement de Biologie Médicale, Centre Scientifique de Monaco, Monaco.
Cyril RoncoUniversité Côte D'Azur, CNRS, Institut de Chimie de Nice UMR 7272, 06108, Nice, France.
Rachid BenhidaUniversité Côte D'Azur, CNRS, Institut de Chimie de Nice UMR 7272, 06108, Nice, France.
Maeva DufiesDépartement de Biologie Médicale, Centre Scientifique de Monaco, Monaco.
Marc FaraggiNuclear Medicine Department, Centre Hospitalier Princesse Grace, Monaco, Monaco.
Gilles PagèsDépartement de Biologie Médicale, Centre Scientifique de Monaco, Monaco.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The chemokine receptors CXCR1/2 play a key role in the aggressiveness of several types of cancers including head and neck squamous cell carcinomas (HNSCCs). In HNSCCs, CXCR1/2 signaling promotes cell proliferation and angiogenesis leading to tumor growth and metastasis. The competitive inhibitor of CXCR1/2, C29, inhibits the growth of experimental HNSCCs in mice. However, a non-invasive tool to monitor treatment response is essential to implement the use of C29 in clinical practices.

Indexed as

18F-FDGChemical inhibitorCXCR1/2HNSCCsPET/CT imaging

Identifiers

PMID34430714
PMCPMC8374394

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.