Nuclear Imaging Study of the Pharmacodynamic Effects of Debio 1143, an Antagonist of Multiple Inhibitor of Apoptosis Proteins (IAPs), in a Triple-Negative Breast Cancer Model
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Titre | Nuclear Imaging Study of the Pharmacodynamic Effects of Debio 1143, an Antagonist of Multiple Inhibitor of Apoptosis Proteins (IAPs), in a Triple-Negative Breast Cancer Model |
Type de publication | Journal Article |
Year of Publication | 2018 |
Auteurs | Bellaye P-S, Oudot A, Vrigneaud J-M, Raguin O, Bichat F, Vaslin A, Hajjami HMaby-El, Zanna C, Vuagniaux G, Fumoleau P, Denat F, Brunotte F, Collin B |
Journal | CONTRAST MEDIA & MOLECULAR IMAGING |
Pagination | UNSP 8494031 |
Type of Article | Article |
ISSN | 1555-4309 |
Résumé | Background. Debio 1143, a potent orally available SMAC mimetic, targets inhibitors of apoptosis proteins (IAPs) members and is currently in clinical trials. In this study, nuclear imaging evaluated the effects of Debio 1143 on tumor cell death and metabolism in a triple-negative breast cancer (TNBC) cell line (MDA-MB-231)-based animal model. Methods. Apoptosis induced by Debio 1143 was assessed by FACS (caspase-3, annexin 5 (A5)), binding of Tc-99m-HYNIC-Annexin V, and a cell proliferation assay. Tc-99m-HYNIC-Annexin V SPECT and [F-18]-FDG PET were also performed in mice xenografted with MDA-MB-231 cells. Results. Debio 1143 induced early apoptosis both in vitro and in vivo 6h after treatment. Debio 1143 inhibited tumor growth, which was associated with a decreased tumor [F-18]-FDG uptake when measured during treatment. Conclusions. This imaging study combining SPECT and PET showed the early proapoptotic effects of Debio 1143 resulting in a robust antitumor activity in a preclinical TNBC model. These imaging biomarkers represent valuable noninvasive tools for translational and clinical research in TNBC. |
DOI | 10.1155/2018/8494031 |