Evidence map›Paper›PMID 30348798›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2018

Self-assembling supramolecular dendrimer nanosystem for PET imaging of tumors.

Philippe Garrigue, Jingjie Tang, Ling Ding, Ahlem Bouhlel, Aura Tintaru, Erik Laurini, Yuanyu Huang, Zhenbin Lyu, Mengjie Zhang, Samantha Fernandez and 11 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

28 citing papers in PubMed.

  1. Fluorinated Amphiphilic Dendrimer to Improve PET Imaging of Cancer.Small (Weinheim an der Bergstrasse, Germany) · 2026
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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

21 authors.

Philippe GarrigueAix-Marseille University, INSERM, INRA, Center de Recherche en Cardiovasculaire et Nutrition (C2VN), 13385 Marseille, France.
Jingjie TangAix-Marseille University, CNRS, Centre Interdisciplinaire de Nanoscience de Marseille (CINaM), Equipe Labellisée Ligue Contre le Cancer, 13288 Marseille, France.
Ling DingAix-Marseille University, CNRS, Centre Interdisciplinaire de Nanoscience de Marseille (CINaM), Equipe Labellisée Ligue Contre le Cancer, 13288 Marseille, France.ORCID 0000-0001-5331-7827
Ahlem BouhlelAix-Marseille University, INSERM, INRA, Center de Recherche en Cardiovasculaire et Nutrition (C2VN), 13385 Marseille, France.
Aura TintaruAix-Marseille University, CNRS, Institut de Chimie Radicalaire (ICR), 13013 Marseille, France.
Erik LauriniMolecular Biology and Nanotechnology Laboratory, Department of Engineering and Architecture, University of Trieste, 34127 Trieste, Italy.ORCID 0000-0001-6092-6532
Yuanyu HuangAdvanced Research Institute of Multidisciplinary Science, Beijing Institute of Technology, Beijing 100081, China.
Zhenbin LyuAix-Marseille University, CNRS, Centre Interdisciplinaire de Nanoscience de Marseille (CINaM), Equipe Labellisée Ligue Contre le Cancer, 13288 Marseille, France.
Mengjie ZhangAdvanced Research Institute of Multidisciplinary Science, Beijing Institute of Technology, Beijing 100081, China.
Samantha FernandezAix-Marseille University, Centre Européen de Recherche en Imagerie Médicale (CERIMED), 13005 Marseille, France.
Laure BalasseAix-Marseille University, INSERM, INRA, Center de Recherche en Cardiovasculaire et Nutrition (C2VN), 13385 Marseille, France.
Wenjun LanAix-Marseille University, CNRS, INSERM, Institut Paoli-Calmettes, Centre de Recherche en Cancériologie de Marseille (CRCM), 13273 Marseille, France.
Eric MasAix-Marseille University, CNRS, INSERM, Institut Paoli-Calmettes, Centre de Recherche en Cancériologie de Marseille (CRCM), 13273 Marseille, France.
Domenico MarsonMolecular Biology and Nanotechnology Laboratory, Department of Engineering and Architecture, University of Trieste, 34127 Trieste, Italy.
Yuhua WengAdvanced Research Institute of Multidisciplinary Science, Beijing Institute of Technology, Beijing 100081, China.
Xiaoxuan LiuAix-Marseille University, CNRS, Centre Interdisciplinaire de Nanoscience de Marseille (CINaM), Equipe Labellisée Ligue Contre le Cancer, 13288 Marseille, France.
Suzanne GiorgioAix-Marseille University, CNRS, Centre Interdisciplinaire de Nanoscience de Marseille (CINaM), Equipe Labellisée Ligue Contre le Cancer, 13288 Marseille, France.
Juan IovannaAix-Marseille University, CNRS, INSERM, Institut Paoli-Calmettes, Centre de Recherche en Cancériologie de Marseille (CRCM), 13273 Marseille, France.
Sabrina PriclMolecular Biology and Nanotechnology Laboratory, Department of Engineering and Architecture, University of Trieste, 34127 Trieste, Italy.ORCID 0000-0001-8380-4474
Benjamin GuilletAix-Marseille University, INSERM, INRA, Center de Recherche en Cardiovasculaire et Nutrition (C2VN), 13385 Marseille, France.
Ling PengAix-Marseille University, CNRS, Centre Interdisciplinaire de Nanoscience de Marseille (CINaM), Equipe Labellisée Ligue Contre le Cancer, 13288 Marseille, France; ling.peng@univ-amu.fr.ORCID 0000-0003-3990-5248

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bioimaging plays an important role in cancer diagnosis and treatment. However, imaging sensitivity and specificity still constitute key challenges. Nanotechnology-based imaging is particularly promising for overcoming these limitations because nanosized imaging agents can specifically home in on tumors via the "enhanced permeation and retention" (EPR) effect, thus resulting in enhanced imaging sensitivity and specificity. Here, we report an original nanosystem for positron emission tomography (PET) imaging based on an amphiphilic dendrimer, which bears multiple PET reporting units at the terminals. This dendrimer is able to self-assemble into small and uniform nanomicelles, which accumulate in tumors for effective PET imaging. Benefiting from the combined dendrimeric multivalence and EPR-mediated passive tumor targeting, this nanosystem demonstrates superior imaging sensitivity and specificity, with up to 14-fold increased PET signal ratios compared with the clinical gold reference 2-fluorodeoxyglucose ([

Indexed as

AnimalsCell Line, TumorColonic NeoplasmsContrast MediaCoordination ComplexesDendrimersFluorodeoxyglucose F18Gallium RadioisotopesGlioblastomaHeterocyclic CompoundsHeterocyclic Compounds, 1-RingHeterograftsHumansMaleMiceMice, Inbred BALB C1,4,7-triazacyclononane-N,N',N''-triacetic acidContrast MediaCoordination ComplexesDendrimersFluorodeoxyglucose F18Gallium RadioisotopesHeterocyclic CompoundsHeterocyclic Compounds, 1-RingbioimagingdendrimerEPR effectsupramolecular nanomicelletumor diagnosis

Identifiers

PMID30348798
PMCPMC6233080

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Registered trials

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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.