Authors
Nathalie Laurent, Sophie de Boüard, Jean-Sébastien Guillamo, Christo Christov, Roland Zini, Hélène Jouault, Patrice Andre, Vincent Lotteau, Marc Peschanski
Publication date
2004/2/1
Journal
Molecular Cancer Therapeutics
Volume
3
Issue
2
Pages
129-136
Publisher
American Association for Cancer Research
Description
Glioblastoma is a therapeutic challenge as a highly infiltrative, proliferative, and resistant tumor. Among novel therapeutic approaches, proteasome inhibition is very promising in controlling cell cycle and inducing apoptosis. This study investigated the effect of ritonavir, a protease inhibitor of the HIV and a proteasome modulator, on glioma cells. The hypothesis was that proteasome modulation, mainly by only inhibiting proteasome chymotrypsin-like activity, could be sufficient to control tumor progression. The experiments were done on a human glioblastoma-derived GL15 cell line and a rat nitrosourea-induced gliosarcoma 9L cell line. Culturing conditions included monolayer cultures, transplantations into brain slices, and transplantations into rat striata. The study demonstrates that ritonavir, by inhibiting the chymotrypsin-like activity of the proteasome, has cytostatic and cytotoxic effects on glioma cells, and can …
Total citations
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Scholar articles
N Laurent, S de Boüard, JS Guillamo, C Christov… - Molecular Cancer Therapeutics, 2004