Evidence map›Paper›PMID 30609832›Full record

ReviewPharmaceuticals (Basel, Switzerland)2019

Radioligands for Tropomyosin Receptor Kinase (Trk) Positron Emission Tomography Imaging.

Ralf Schirrmacher, Justin J Bailey, Andrew V Mossine, Peter J H Scott, Lena Kaiser, Peter Bartenstein, Simon Lindner, David R Kaplan, Alexey Kostikov, Gert Fricker and 8 more

Abstract readReview
In one paragraph

Review in Pharmaceuticals (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
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

18 authors.

Ralf SchirrmacherDepartment of Oncology, Division of Oncological Imaging, University of Alberta, Edmonton, Alberta T6G 2R3, Canada. schirrma@ualberta.ca.ORCID 0000-0002-7098-3036
Justin J BaileyDepartment of Oncology, Division of Oncological Imaging, University of Alberta, Edmonton, Alberta T6G 2R3, Canada. jjbailey@ualberta.ca.
Andrew V MossineDivision of Nuclear Medicine, Department of Radiology, The University of Michigan Medical School, Ann Arbor, MI, 48109, USA. amossine@med.umich.edu.
Peter J H ScottDivision of Nuclear Medicine, Department of Radiology, The University of Michigan Medical School, Ann Arbor, MI, 48109, USA. pjhscott@med.umich.edu.ORCID 0000-0002-6505-0450
Lena KaiserDepartment of Nuclear Medicine, Ludwig-Maximilians-University of Munich, Marchioninistrasse 15, Munich 81377, Germany. Lena.Kaiser@med.uni-muenchen.de.ORCID 0000-0002-2084-5858
Peter BartensteinDepartment of Nuclear Medicine, Ludwig-Maximilians-University of Munich, Marchioninistrasse 15, Munich 81377, Germany. Peter.Bartenstein@med.uni-muenchen.de.
Simon LindnerDepartment of Nuclear Medicine, Ludwig-Maximilians-University of Munich, Marchioninistrasse 15, Munich 81377, Germany. Simon.Lindner@med.uni-muenchen.de.
David R KaplanProgram in Neurosciences and Mental Health, Hospital for Sick Children and Department of Molecular Genetics, University of Toronto, Toronto, ON, Canada M5G 0A4. dkaplan@sickkids.ca.
Alexey KostikovMcConnell Brain Imaging Centre, Montreal Neurological Institute, McGill University, 3801 University Street, Montreal, QC H3A 2B4, Canada. alexey.kostikov@mcgill.ca.
Gert FrickerInstitute of Pharmacy and Molecular Biotechnology, University of Heidelberg, Heidelberg 69120, Germany. gert.fricker@uni-hd.de.
Anne MahringerInstitute of Pharmacy and Molecular Biotechnology, University of Heidelberg, Heidelberg 69120, Germany. mahringer@uni-hd.de.
Pedro Rosa-NetoTranslational Neuroimaging Laboratory, McGill Centre for Studies in Aging, Douglas Mental Health University Institute, Montreal, QC H4H 1R3, Canada. pedro.rosa.neto@gmail.com.
Esther SchirrmacherDepartment of Oncology, Division of Oncological Imaging, University of Alberta, Edmonton, Alberta T6G 2R3, Canada. eschirrm@ualberta.ca.
Carmen WänglerBiomedical Chemistry, Department of Clinical Radiology and Nuclear Medicine, Medical Faculty Mannheim of Heidelberg University, 68167 Mannheim, Germany. Carmen.Waengler@medma.uni-heidelberg.de.
Björn WänglerMolecular Imaging and Radiochemistry, Department of Clinical Radiology and Nuclear Medicine, Medical Faculty Mannheim of Heidelberg University, Theodor-Kutzer-Ufer 1-3, Mannheim 68167, Germany. Bjoern.Waengler@medma.uni-heidelberg.de.
Alexander ThielMcConnell Brain Imaging Centre, Montreal Neurological Institute, McGill University, 3801 University Street, Montreal, QC H3A 2B4, Canada. alexander.thiel@mcgill.ca.
Jean-Paul SoucyMcConnell Brain Imaging Centre, Montreal Neurological Institute, McGill University, 3801 University Street, Montreal, QC H3A 2B4, Canada. jean-paul.soucy@mcgill.ca.
Vadim Bernard-GauthierAzrieli Centre for Neuro-Radiochemistry, Research Imaging Centre, Centre for Addiction and Mental Health, Toronto, ON M5T 1L8, Canada. Vadim.bernard-gauthier@camhpet.ca.

Funding

Cancer Research Society and C17 Council 21007Natural Sciences and Engineering Research Council of Canada 327872U.S. Department of Energy DE-SC0012484Weston Brain Institute RR161057
6 · The paper itself

Abstract

The tropomyosin receptor kinases family (TrkA, TrkB, and TrkC) supports neuronal growth, survival, and differentiation during development, adult life, and aging. TrkA/B/C downregulation is a prominent hallmark of various neurological disorders including Alzheimer's disease (AD). Abnormally expressed or overexpressed full-length or oncogenic fusion TrkA/B/C proteins were shown to drive tumorigenesis in a variety of neurogenic and non-neurogenic human cancers and are currently the focus of intensive clinical research. Neurologic and oncologic studies of the spatiotemporal alterations in TrkA/B/C expression and density and the determination of target engagement of emerging antineoplastic clinical inhibitors in normal and diseased tissue are crucially needed but have remained largely unexplored due to the lack of suitable non-invasive probes. Here, we review the recent development of carbon-11- and fluorine-18-labeled positron emission tomography (PET) radioligands based on specifically designed small molecule kinase catalytic domain-binding inhibitors of TrkA/B/C. Basic developments in medicinal chemistry, radiolabeling and translational PET imaging in multiple species including humans are highlighted.

Indexed as

neurodegenerationoncogenic fusionspositron emission tomographytropomyosin receptor kinase

Identifiers

PMID30609832
PMCPMC6469173

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.