How to Modulate Tumor Hypoxia for Preclinical In Vivo Imaging Research

Author:

De Bruycker Sven1ORCID,Vangestel Christel12,Staelens Steven1,Van den Wyngaert Tim12,Stroobants Sigrid12ORCID

Affiliation:

1. Molecular Imaging Center Antwerp (MICA), University of Antwerp, Universiteitsplein 1, 2610 Wilrijk, Antwerp, Belgium

2. Department of Nuclear Medicine, Antwerp University Hospital (UZA), Wilrijkstraat 10, 2650 Edegem, Antwerp, Belgium

Abstract

Tumor hypoxia is related with tumor aggressiveness, chemo- and radiotherapy resistance, and thus a poor clinical outcome. Therefore, over the past decades, every effort has been made to develop strategies to battle the negative prognostic influence of tumor hypoxia. For appropriate patient selection and follow-up, noninvasive imaging biomarkers such as positron emission tomography (PET) radiolabeled ligands are unprecedentedly needed. Importantly, before being able to implement these new therapies and potential biomarkers into the clinical setting, preclinical in vivo validation in adequate animal models is indispensable. In this review, we provide an overview of the different attempts that have been made to create differential hypoxic in vivo cancer models with a particular focus on their applicability in PET imaging studies.

Funder

Universiteit Antwerpen

Publisher

Hindawi Limited

Subject

Radiology Nuclear Medicine and imaging

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