Evidence map›Paper›PMID 32060400›Full record

ArticleScientific reports2020

Development of an embedded multimodality imaging platform for onco-pharmacology using a smart anticancer prodrug as an example.

Florian Raes, Serigne Moussa Badiane, Brigitte Renoux, Sébastien Papot, Stéphanie Lerondel, Alain Le Pape

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 40% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Article
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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

6 authors at 3 institutions in 3 countries.

Florian RaesInstitute for Cancer Research, ICR, Sutton, London, United Kingdom. florian.raes@icr.ac.uk.ORCID http://orcid.org/0000-0003-2898-995X
Serigne Moussa BadianeUFR des Sciences de la Santé, Université Gaston Berger, Saint-Louis, Senegal.
Brigitte RenouxIC2MP, Chemistry Institute of Poitiers: Materials and Natural Ressources; Programmed Molecular Systems Team, UMR-CNRS 7285, Poitiers, France.
Sébastien PapotIC2MP, Chemistry Institute of Poitiers: Materials and Natural Ressources; Programmed Molecular Systems Team, UMR-CNRS 7285, Poitiers, France.
Stéphanie LerondelCentre for Small Animal Imaging, CIPA, Phenomin-TAAM CNRS UPS44, Orléans, France.
Alain Le PapeCentre for Small Animal Imaging, CIPA, Phenomin-TAAM CNRS UPS44, Orléans, France.
Centre National de la Recherche Scientifique · FRUniversité d'Orléans · FRUniversité Gaston Berger · SN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Increasingly, in vivo imaging holds a strategic position in bio-pharmaceutical innovation. We will present the implementation of an integrated multimodal imaging setup enabling the assessment of multiple, complementary parameters. The system allows the fusion of information provided by: Near infrared fluorescent biomarkers, bioluminescence (for tumor proliferation status), Photoacoustic and Ultrasound imaging. We will study representative applications to the development of a smart prodrug, delivering a highly cytotoxic chemotherapeutic agent to cancer tumors. The results realized the ability of this embedded, multimodality imaging platform to firstly detect bioluminescent and fluorescent signals, and secondly, record ultrasound and photoacoustic data from the same animal. This study demonstrated that the prodrug was effective in three different models of hypoxia in human cancers compared to the parental cytotoxic agent and the vehicle groups. Monitoring by photoacoustic imaging during the treatments revealed that the prodrug exhibits an intrinsic capability to prevent the progression of tumor hypoxia. It is essential for onco-pharmacology studies to precisely document the hypoxic status of tumors both before and during the time course of treatments. This approach opens new perspectives for exploitation of preclinical mouse models of cancer, especially when considering associations between hypoxia, neoangiogenesis and antitumor activity.

Indexed as

Multimodal ImagingAnimalsAntineoplastic AgentsCell Line, TumorFemaleHumansMice, Inbred BALB CMice, NudeNeoplasmsProdrugsTumor HypoxiaXenograft Model Antitumor AssaysAntineoplastic AgentsProdrugs

Identifiers

PMID32060400
PMCPMC7021674
OpenAlexW3006460991

What OpenQuestion holds

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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.