%0 Journal Article %1 Charest2010 %A Charest, Gabriel %A Paquette, Benoit %A Fortin, David %A Mathieu, David %A Sanche, Léon %D 2010 %J J Neurooncol %K administration/&/dosage;Carboplatin administration/&/dosage;Radiotherapy;Rats Tumor;Cisplatin Animals;AntineoplasticAgents Ionizing;Radiation-SensitizingAgents drugtherapy/radiotherapy;InhibitoryConcentration50;Liposomes;Radiation administration/&/dosage;CellLine pharmacology;CombinedModalityTherapy;Glioma %N 2 %P 187--193 %R 10.1007/s11060-009-0011-5 %T Concomitant treatment of F98 glioma cells with new liposomal platinum compounds and ionizing radiation. %U http://dx.doi.org/10.1007/s11060-009-0011-5 %V 97 %X Despite significant advances, the radiotherapy and chemotherapy protocols marginally improve the overall survival of patients with glioblastoma. Lipoplatin(TM), and Lipoxal(TM), the liposomal formulations of cisplatin and oxaliplatin respectively, were tested on the F98 glioma cells for their ability to improve the cell uptake and increase the synergic effect when combined with ionizing radiation. The cytotoxicity and synergic effect of platinum compounds were assessed by colony formation assay, while the cellular uptake was measured by Inductively Coupled Plasma Mass Spectrometer (ICP-MS). After 4 h exposure with platinum compounds, cells were irradiated (1.5-6.6 Gy) with a (60)Co source. The liposomal formulations were compared to their liposome-free analogs and to carboplatin. The concomitant treatment of F98 cells with carboplatin and radiation produced the highest radiosensitizing effect (30-fold increase). Among the platinum compounds tested, Lipoplatin(TM) produced the most promising results. This liposomal formulation of cisplatin improved the cell uptake by 3-fold, and its radiosensitizing potential was enhanced by 14-fold. Although Lipoxal(TM) can potentially reduce the adverse effect of oxaliplatin, a synergic effect with radiation was measured only when incubated at a concentration higher than its IC50. Conversely, concomitant treatment with cisplatin did not result in a synergic effect, as in fact a radioprotective effect was measured on the F98 cells. In conclusion, among the five platinum compounds tested, carboplatin and Lipoplatin(TM) showed the best radiosensitizing effect. Lipoplatin(TM) seems the most promising since it led to the best cellular incorporation and has already been reported to be less neurotoxic than other platinum compounds.

@article{Charest2010, abstract = {Despite significant advances, the radiotherapy and chemotherapy protocols marginally improve the overall survival of patients with glioblastoma. Lipoplatin(TM), and Lipoxal(TM), the liposomal formulations of cisplatin and oxaliplatin respectively, were tested on the F98 glioma cells for their ability to improve the cell uptake and increase the synergic effect when combined with ionizing radiation. The cytotoxicity and synergic effect of platinum compounds were assessed by colony formation assay, while the cellular uptake was measured by Inductively Coupled Plasma Mass Spectrometer (ICP-MS). After 4 h exposure with platinum compounds, cells were irradiated (1.5-6.6 Gy) with a (60)Co source. The liposomal formulations were compared to their liposome-free analogs and to carboplatin. The concomitant treatment of F98 cells with carboplatin and radiation produced the highest radiosensitizing effect (30-fold increase). Among the platinum compounds tested, Lipoplatin(TM) produced the most promising results. This liposomal formulation of cisplatin improved the cell uptake by 3-fold, and its radiosensitizing potential was enhanced by 14-fold. Although Lipoxal(TM) can potentially reduce the adverse effect of oxaliplatin, a synergic effect with radiation was measured only when incubated at a concentration higher than its IC50. Conversely, concomitant treatment with cisplatin did not result in a synergic effect, as in fact a radioprotective effect was measured on the F98 cells. In conclusion, among the five platinum compounds tested, carboplatin and Lipoplatin(TM) showed the best radiosensitizing effect. Lipoplatin(TM) seems the most promising since it led to the best cellular incorporation and has already been reported to be less neurotoxic than other platinum compounds.}, added-at = {2011-07-21T21:36:17.000+0200}, author = {Charest, Gabriel and Paquette, Benoit and Fortin, David and Mathieu, David and Sanche, Léon}, biburl = {https://www.bibsonomy.org/bibtex/2c41fe090e97cc25df39b18a74810cd7b/crc_chus}, doi = {10.1007/s11060-009-0011-5}, institution = {Université de Sherbrooke, Sherbrooke, Canada.}, interhash = {eafe412b8b19ab28ac6b766e48501608}, intrahash = {c41fe090e97cc25df39b18a74810cd7b}, journal = {J Neurooncol}, keywords = {administration/&/dosage;Carboplatin administration/&/dosage;Radiotherapy;Rats Tumor;Cisplatin Animals;AntineoplasticAgents Ionizing;Radiation-SensitizingAgents drugtherapy/radiotherapy;InhibitoryConcentration50;Liposomes;Radiation administration/&/dosage;CellLine pharmacology;CombinedModalityTherapy;Glioma}, language = {eng}, medline-pst = {ppublish}, month = Apr, number = 2, pages = {187--193}, pmid = {19760366}, timestamp = {2011-07-21T21:36:17.000+0200}, title = {Concomitant treatment of F98 glioma cells with new liposomal platinum compounds and ionizing radiation.}, url = {http://dx.doi.org/10.1007/s11060-009-0011-5}, volume = 97, year = 2010 }