Concomitant treatment of F98 glioma cells with new liposomal platinum compounds and ionizing radiation

被引:40
作者
Charest, Gabriel [1 ]
Paquette, Benoit [1 ]
Fortin, David [1 ]
Mathieu, David [1 ]
Sanche, Leon [1 ]
机构
[1] Univ Sherbrooke, Sherbrooke, PQ J1K 2R1, Canada
基金
加拿大健康研究院;
关键词
Platinum compounds; Liposomes; Gamma radiation; Glioma; Synergy; PHASE-I; CISPLATIN LIPOPLATIN; CARBOPLATIN; OXALIPLATIN; CARCINOMA; THERAPY; CANCER; CHEMOTHERAPY; RADIOTHERAPY; INFUSION;
D O I
10.1007/s11060-009-0011-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 Co-60 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.
引用
收藏
页码:187 / 193
页数:7
相关论文
共 25 条
[2]  
Boulikas T, 2005, ANTICANCER RES, V25, P3031
[3]  
Boulikas T, 2004, ONCOL REP, V12, P3
[4]  
Boulikas T, 2003, ONCOL REP, V10, P1663
[5]  
Boulikas T., 2007, Cancer ther, V5, P349
[6]  
Chakravarti Arnab, 2008, P173
[7]   Theoretical basis, experimental design, and computerized simulation of synergism and antagonism in drug combination studies [J].
Chou, Ting-Chao .
PHARMACOLOGICAL REVIEWS, 2006, 58 (03) :621-681
[8]   Phase I trial of oxaliplatin with fluorouracil, folinic acid and concurrent radiotherapy for oesophageal cancer [J].
Conroy, T. ;
Viret, F. ;
Francois, E. ;
Seitz, J. F. ;
Boige, V. ;
Ducreux, M. ;
Ychou, M. ;
Metges, J. P. ;
Giovannini, M. ;
Yataghene, Y. ;
Peiffert, D. .
BRITISH JOURNAL OF CANCER, 2008, 99 (09) :1395-1401
[9]   Enhanced chemotherapy delivery by intraarterial infusion and blood-brain barrier disruption in malignant brain tumors: The sherbrooke experience [J].
Fortin, D ;
Desjardins, A ;
Benko, A ;
Niyonsega, T ;
Boudrias, M .
CANCER, 2005, 103 (12) :2606-2615
[10]   Uptake of antitumor platinum(II)-complexes by cancer cells, assayed by inductively coupled plasma mass spectrometry (ICP-MS) [J].
Ghezzi, A ;
Aceto, M ;
Cassino, C ;
Gabano, E ;
Osella, D .
JOURNAL OF INORGANIC BIOCHEMISTRY, 2004, 98 (01) :73-78