Structure-Based Design of a Lead Compound Derived from Natural Schweinfurthins with Antitumor Properties That Target Oxysterol-Binding Protein

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Jézéquel, Gwenaëlle | Rampal, Céline | Guimard, Carole | Kovacs, David | Polidori, Joël | Bigay, Joëlle | Bignon, Jérôme | Askenatzis, Laurie | Litaudon, Marc | Pruvost, Alain | Pham, Van-Cuong | Doan Thi Mai, Huong | Nguyen, Anvi Laetitia | Virolle, Thierry | Mesmin, Bruno | Desrat, Sandy | Antonny, Bruno | Roussi, Fanny

Edité par CCSD ; American Chemical Society -

International audience. Schweinfurthins (SWs) are naturally occurring prenylated stilbenes with promising anticancer properties. They act through a novel mechanism of action similar to that of other families of natural compounds. Their known target, oxysterol-binding protein (OSBP), plays a crucial role in controlling the intracellular distribution of cholesterol. We synthesized 15 analogues of SWs and demonstrated for the first time that their cytotoxicity as well as that of natural derivatives correlates with their affinity for OSBP. Through this extensive SAR study, we selected one synthetic analogue obtained in one step from SW-G. Using its fluorescence properties, we showed that this compound recapitulates the effect of natural SW-G in cells and confirmed that it leads to cell death via the same mechanism. Finally, after pilot PK experiments, we provided the first evidence of its in vivo efficacy in combination with temozolomide in a patient-derived glioblastoma xenograft model.

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