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Published Online: 19 April 2016

Efficacy Screening of Gloriosa Superba Extracts in a Murine Pancreatic Cancer Model Using 18F-FDG PET/CT for Monitoring Treatment Response

Publication: Cancer Biotherapy and Radiopharmaceuticals
Volume 31, Issue Number 3

Abstract

Purpose: In vivo efficacy of two herbal extracts of Gloriosa superba L. (Colchicaceae) was investigated in a murine pancreatic tumor model by tumor volume measurements and Positron Emission Tomography (PET) imaging using 2-deoxy-2-[18F]fluoro-d-glucose (18F-FDG).
Materials and Methods: A crude extract of G. superba (GS) seeds rich in colchicine and a colchicine-poor extract (GS2B) containing mostly colchicoside as a putative prodrug were prepared. PANC02-bearing C57BL/6 mice were treated with either placebo, gemcitabine, or one of the extracts (three different doses) for 10 days. Tumor volume measurements were performed daily during treatment and additionally 18F-FDG Positron emission tomography/computed tomography was acquired at baseline and after 7 days of treatment. Ki-67 and cleaved caspase-3 immunostaining was performed on the resected tumors.
Results: After 7 days of treatment, a dose-dependent tumor growth inhibition of both extracts was observed with the highest in vivo response at the highest dose of GS and GS2B and gemcitabine. A positive significant correlation was found between Ki-67 scores and relative tumor volumes (RTV), and a negative significant correlation between caspase-3 staining scores and RTV. A decrease in 18F-FDG uptake was clearly observed in all treatment groups.
Conclusions: The therapeutic efficacy of the two different herbal extracts was demonstrated in an in vivo pancreatic tumor model. 18F-FDG PET was able to detect an early response as overall lower 18F-FDG uptake was measured in the treated groups.

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Published In

cover image Cancer Biotherapy and Radiopharmaceuticals
Cancer Biotherapy and Radiopharmaceuticals
Volume 31Issue Number 3April 2016
Pages: 99 - 109
PubMed: 27093343

History

Published online: 19 April 2016
Published in print: April 2016

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    Authors

    Affiliations

    Rica Capistrano*
    Department of Pharmaceutical Sciences, Natural Products & Food Research and Analysis (NatuRA), University of Antwerp, Antwerp, Belgium.
    Christel Vangestel*
    Department of Nuclear Medicine, Antwerp University Hospital, Edegem, Belgium.
    Molecular Imaging Center Antwerp (MICA), University of Antwerp, Antwerp, Belgium.
    An Wouters
    Center for Oncological Research (CORE), University of Antwerp, Antwerp, Belgium.
    Yanina Dockx
    Molecular Imaging Center Antwerp (MICA), University of Antwerp, Antwerp, Belgium.
    Patrick Pauwels
    Center for Oncological Research (CORE), University of Antwerp, Antwerp, Belgium.
    Sigrid Stroobants
    Department of Nuclear Medicine, Antwerp University Hospital, Edegem, Belgium.
    Molecular Imaging Center Antwerp (MICA), University of Antwerp, Antwerp, Belgium.
    Sandra Apers
    Department of Pharmaceutical Sciences, Natural Products & Food Research and Analysis (NatuRA), University of Antwerp, Antwerp, Belgium.
    Filip Lardon
    Center for Oncological Research (CORE), University of Antwerp, Antwerp, Belgium.
    Luc Pieters*
    Department of Pharmaceutical Sciences, Natural Products & Food Research and Analysis (NatuRA), University of Antwerp, Antwerp, Belgium.
    Steven Staelens*
    Molecular Imaging Center Antwerp (MICA), University of Antwerp, Antwerp, Belgium.

    Notes

    *
    These authors contributed equally to this work.
    Address correspondence to: Steven Staelens; Molecular Imaging Center Antwerp (MICA), University of Antwerp; Antwerp, Wilrijk 2610, Belgium
    E-mail: [email protected]

    Disclosure Statement

    No competing financial interests exist.

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