Survival of human glioma cells treated with various combination of temozolomide and X-rays

被引:154
作者
van Rijn, J
Heimans, JJ
van den Berg, J
van der Valk, P
Slotman, BJ
机构
[1] Vrije Univ Amsterdam, Acad Ziekenhuis, Dept Radiat Oncol, NL-1007 MB Amsterdam, Netherlands
[2] Vrije Univ Amsterdam, Acad Ziekenhuis, Dept Neurol, NL-1007 MB Amsterdam, Netherlands
[3] Vrije Univ Amsterdam, Acad Ziekenhuis, Dept Pathol, NL-1007 MB Amsterdam, Netherlands
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2000年 / 47卷 / 03期
关键词
human glioma cells; temozolomide; X-rays; cell survival;
D O I
10.1016/S0360-3016(99)00539-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To investigate the effect of temozolomide, a 3-methyl derivative of mitozolomide in combination with X-rays in human glioma-derived cell lines. Methods and Materials: Glioma cell lines D384 and U251 were treated with temozolomide for various periods of time in combinations with X-rays. Temozolomide administration was repeated every 24 h for exposures up to 96 h. Cytotoxicity was determined with a clonogenic assay. Results: Incubation of D384 cells with temozolomide during 24 h prior to or following irradiation results in a moderate enhancement of the cytotoxicity. Prolonged treatment with temozolomide, i.e., 48-96 h before X-rays, causes a stronger potentiation. In contrast, no enhancement is observed in irradiated U251 cells in combination with 24-96 h temozolomide treatment. In addition to single-dose irradiation, rye investigated the effect of temozolomide in D384 cells with concomitant fractionated irradiation. A 96-h exposure to temozolomide with simultaneous doses of 2 Gy X-rays at 24-h intervals, causes a significant further reduction in cell survival as compared to fractionated irradiation only. Conclusion: Depending on the cell line, treatment of glioma cells with temozolomide and X-rays can have either an additional effect or potentiate cell killing. (C) 2000 Elsevier Science Inc.
引用
收藏
页码:779 / 784
页数:6
相关论文
共 25 条
[1]   Principles of treatment of malignant gliomas in adults: An overview [J].
Azizi, SA ;
Miyamoto, C .
JOURNAL OF NEUROVIROLOGY, 1998, 4 (02) :204-216
[2]  
BALMFORTH AJ, 1986, J NEUROCHEM, V47, P515
[3]   Multicentre CRC phase II trial of temozolomide in recurrent or progressive high-grade glioma [J].
Bower, M ;
Newlands, ES ;
Bleehen, NM ;
Brada, M ;
Begent, RJH ;
Calvert, H ;
Colquhoun, I ;
Lewis, P ;
Brampton, MH .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 1997, 40 (06) :484-488
[4]   Current perspectives in gliomas [J].
Brock, CS ;
Bower, M .
MEDICAL ONCOLOGY, 1997, 14 (02) :103-120
[5]   ROLE OF GLUTATHIONE IN THE RADIATION RESPONSE OF MAMMALIAN-CELLS INVITRO AND INVIVO [J].
BUMP, EA ;
BROWN, JM .
PHARMACOLOGY & THERAPEUTICS, 1990, 47 (01) :117-136
[6]  
CATAPANO CV, 1987, CANCER RES, V47, P4884
[7]   INDUCTION AND PURIFICATION OF O-6-METHYLGUANINE-DNA-METHYLTRANSFERASE FROM RAT-LIVER [J].
CHAN, CL ;
WU, ZN ;
EASTMAN, A ;
BRESNICK, E .
CARCINOGENESIS, 1990, 11 (07) :1217-1221
[8]   Phase I study of temozolomide in paediatric patients with advanced cancer [J].
Estlin, EJ ;
Lashford, L ;
Ablett, S ;
Price, L ;
Gowing, R ;
Gholkar, A ;
Kohler, J ;
Lewis, IJ ;
Morland, B ;
Pinkerton, CR ;
Stevens, R ;
Mott, M ;
Stevens, R ;
Newell, DR ;
Walker, D ;
Dicks-Mireaux, C ;
McDowell, H ;
Reidenberg, P ;
Statkevich, P ;
Marco, A ;
Batra, V ;
Dugan, N ;
Pearson, ADJ .
BRITISH JOURNAL OF CANCER, 1998, 78 (05) :652-661
[9]  
FRUEHAUF JP, 1998, P AM SOC CLIN ONCOL, V17, pA198
[10]  
FRUEHAUF JP, 1998, P AM SOC CLIN ONCOL, V17, P763