Title of article :
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
Author/Authors :
Bellaye, Pierre-Simon Centre Georges-François Leclerc - Dijon, France , Oudot, Alexandra Centre Georges-François Leclerc - Dijon, France , Vrigneaud, Jean-Marc Centre Georges-François Leclerc - Dijon, France , Raguin, Olivier Oncodesign - Dijon, France , Bichat, Francis Oncodesign - Dijon, France , Vaslin, Anne Debiopharm International SA - Lausanne, Switzerland , Hajjami, Helene Maby-El Debiopharm International SA - Lausanne, Switzerland , Zanna, Claudio Debiopharm International SA - Lausanne, Switzerland , Vuagniaux, Gregoire Debiopharm International SA - Lausanne, Switzerland , Fumoleau, Pierre Centre Georges-François Leclerc - Dijon, France , Denat, Franck ICMUB - Dijon, France , Brunotte, François Centre Georges-François Leclerc - Dijon, France , Collin, Bertrand Centre Georges-François Leclerc - Dijon, France
Abstract :
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 efiects 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 99mTc-HYNIC-Annexin V, and a cell proliferation assay. 99mTcHYNIC-Annexin V SPECT and [18F]-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 6 h after treatment. Debio 1143 inhibited tumor growth, which was
associated with a decreased tumor [18F]-FDG uptake when measured during treatment. Conclusions. is imaging study
combining SPECT and PET showed the early proapoptotic efiects of Debio 1143 resulting in a robust antitumor activity in
a preclinical TNBC model. ese imaging biomarkers represent valuable noninvasive tools for translational and clinical research
in TNBC.
Keywords :
IAPs , Pharmacodynamic , SMAC , WHO , TNBC