Exendin-4 analogs in insulinoma theranostics.

GLP-1 receptor exendin-4 insulinoma peptide receptor radionuclide therapy (PRRT) positron emission tomography (PET) single-photon emission computed tomography (SPECT) targeted photodynamic therapy (tPDT) theranostics

Journal

Journal of labelled compounds & radiopharmaceuticals
ISSN: 1099-1344
Titre abrégé: J Labelled Comp Radiopharm
Pays: England
ID NLM: 7610510

Informations de publication

Date de publication:
08 2019
Historique:
received: 07 01 2019
revised: 24 04 2019
accepted: 03 05 2019
pubmed: 10 5 2019
medline: 12 5 2020
entrez: 10 5 2019
Statut: ppublish

Résumé

Insulinomas, neuroendocrine tumors arising from pancreatic beta cells, often show overexpression of the glucagon-like peptide-1 receptor. Therefore, imaging with glucagon-like peptide analog exendin-4 can be used for diagnosis and preoperative localization. This review presents an overview of the development and clinical implementation of exendin-based tracers for nuclear imaging, and the potential use of exendin-4 based tracers for optical imaging and therapeutic applications such as peptide receptor radionuclide therapy or targeted photodynamic therapy. Insulinomas are neuroendocrine tumors arising from the pancreatic beta cells. Currently, surgical resection is the therapy of choice, and therefore, preoperative localization of insulinomas is essential. Nearly all insulinomas show overexpression of the glucagon-like peptide-1 receptor (GLP-1R), and therefore, radiolabeled GLP-1 peptide analog exendin-4 can be used for diagnosis and preoperative localization with nuclear imaging. Here, we present an overview of the development and clinical implementation of exendin-4-based tracers for single-photon emission computed tomography (SPECT) and positron emission tomography (PET) imaging of insulinomas, and we address the potential use of this molecule for optical imaging. At last, we discuss the possibilities and pitfalls of the use of exendin-4-based tracers for therapeutic applications such as peptide receptor radionuclide therapy (PRRT) or targeted photodynamic therapy (tPDT), giving a future outlook on the use of exendin-4 in insulinoma theranostics.

Autres résumés

Type: Publisher (dut)
Insulinomas are neuroendocrine tumors arising from the pancreatic beta cells. Currently, surgical resection is the therapy of choice, and therefore, preoperative localization of insulinomas is essential. Nearly all insulinomas show overexpression of the glucagon-like peptide-1 receptor (GLP-1R), and therefore, radiolabeled GLP-1 peptide analog exendin-4 can be used for diagnosis and preoperative localization with nuclear imaging. Here, we present an overview of the development and clinical implementation of exendin-4-based tracers for single-photon emission computed tomography (SPECT) and positron emission tomography (PET) imaging of insulinomas, and we address the potential use of this molecule for optical imaging. At last, we discuss the possibilities and pitfalls of the use of exendin-4-based tracers for therapeutic applications such as peptide receptor radionuclide therapy (PRRT) or targeted photodynamic therapy (tPDT), giving a future outlook on the use of exendin-4 in insulinoma theranostics.

Identifiants

pubmed: 31070270
doi: 10.1002/jlcr.3750
pmc: PMC6771680
doi:

Substances chimiques

Exenatide 9P1872D4OL

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

656-672

Subventions

Organisme : BetaCure
ID : FP7/2014-2018, grant agreement 602812
Pays : International
Organisme : INNODIA
ID : IMI2-JU, grant agreement 115797
Pays : International

Informations de copyright

© 2019 The Authors Journal of Labelled Compounds and Radiopharmaceuticals Published by John Wiley & Sons Ltd.

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Auteurs

Tom J P Jansen (TJP)

Department of Radiology and Nuclear Medicine, Radboudumc, Nijmegen, The Netherlands.

Sanne A M van Lith (SAM)

Department of Radiology and Nuclear Medicine, Radboudumc, Nijmegen, The Netherlands.

Marti Boss (M)

Department of Radiology and Nuclear Medicine, Radboudumc, Nijmegen, The Netherlands.

Maarten Brom (M)

Department of Radiology and Nuclear Medicine, Radboudumc, Nijmegen, The Netherlands.

Lieke Joosten (L)

Department of Radiology and Nuclear Medicine, Radboudumc, Nijmegen, The Netherlands.

Martin Béhé (M)

Center for Radiopharmaceutical Sciences ETH-PSI-USZ, Paul Scherrer Institute, Villigen, Switzerland.

Mijke Buitinga (M)

Department of Radiology and Nuclear Medicine, Radboudumc, Nijmegen, The Netherlands.
Department of Clinical and Experimental Medicine, KU Leuven, Leuven, Belgium.

Martin Gotthardt (M)

Department of Radiology and Nuclear Medicine, Radboudumc, Nijmegen, The Netherlands.

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