Effect of treatment schedule on the interaction of cisplatin and radiation in human lung cancer cells

被引:9
作者
Asaka-Amano, Yoshiko [1 ]
Takiguchi, Yuichi [1 ]
Yatomi, Mari [1 ]
Kurosu, Katsushi [1 ]
Kasahara, Yasunori [1 ]
Tanabe, Nobuhiro [1 ]
Tatsumi, Koichiro [1 ]
Kuriyama, Takayuki [1 ]
机构
[1] Chiba Univ, Dept Respirol B2, Grad Sch Med, Chuo Ku, Chiba 2608670, Japan
关键词
D O I
10.1667/RR0739.1
中图分类号
Q [生物科学];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
This study was designed to determine the effects of the treatment schedule on the interaction between cisplatin and radiation. Cells of a human squamous cell lung cancer cell line were treated with cisplatin and radiation using three treatment protocols: 1-h exposure to cisplatin immediately followed by irradiation (A), 4-day continuous exposure to cisplatin immediately followed by irradiation (B), and 1-h exposure to cisplatin followed by irradiation after a 4-day interval (C). The interactions were assessed by isobologram, cell cycle distribution and apoptosis. The combination resulted in a additive effect in every protocol. Cell cycle accumulation at G(2)/M phase before irradiation was observed in Protocols B and C, whereas no cell cycle shift in the limited time course was noted in Protocol A. Although a 4-day continuous exposure to cisplatin and a 1-h exposure to cisplatin followed by a 4-day interval before irradiation caused significantly increased apoptosis, an additional increase in apoptosis after irradiation was not observed in Protocols B and C, whereas Protocol A showed an additional increase. Despite a cell cycle shift favoring radiation sensitivity, the drug-radiation interactions in Protocols B and C were additive, possibly because of negative effects including induction of a durable G(2)/M-phase arrest and suppression of apoptosis by cisplatin. (C) 2007 by Radiation Research Society
引用
收藏
页码:637 / 644
页数:8
相关论文
共 43 条
[1]
ALVAREZ MV, 1978, BRIT J CANCER, V37, P68
[2]
G2 and spindle assembly checkpoint adaptation, and tetraploidy arrest: Implications for intrinsic and chemically induced genomic instability [J].
Andreassen, PR ;
Lohez, OD ;
Margolis, RL .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2003, 532 (1-2) :245-253
[3]
DOSE FRACTIONATION, DOSE-RATE AND ISO-EFFECT RELATIONSHIPS FOR NORMAL TISSUE RESPONSES [J].
BARENDSEN, GW .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1982, 8 (11) :1981-1997
[4]
THERAPEUTIC ENHANCEMENT IN MICE BY CLINICALLY RELEVANT DOSE AND FRACTIONATION SCHEDULES OF CIS-DIAMMINEDICHLOROPLATINUM(II) AND IRRADIATION [J].
BARTELINK, H ;
KALLMAN, RF ;
RAPACCHIETTA, D ;
HART, GAM .
RADIOTHERAPY AND ONCOLOGY, 1986, 6 (01) :61-74
[5]
THE EFFECT OF CISPLATIN ON THE REPAIR OF RADIATION-DAMAGE IN RIF1 MOUSE-TUMORS INVIVO [J].
BEGG, AC ;
BOHLKEN, S ;
BARTELINK, H .
RADIOTHERAPY AND ONCOLOGY, 1989, 15 (01) :79-91
[6]
RADIOSENSITIZATION BY CISPLATIN OF RIF1 TUMOR-CELLS INVITRO [J].
BEGG, AC ;
VANDERKOLK, PJ ;
DEWIT, L ;
BARTELINK, H .
INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, 1986, 50 (05) :871-884
[7]
THE EFFECT OF COMBINATION TREATMENT WITH CIS-PLATINUM AND LOW-DOSE RATE I-125 RADIATION IN A MURINE BRACHYTHERAPY MODEL [J].
DASILVA, V ;
GUTIN, PH ;
BARCELLOSHOFF, MH ;
BERNSTEIN, MA ;
DEEN, DF ;
WEAVER, KA .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1984, 10 (08) :1471-1472
[8]
COMBINED TREATMENT OF RADIATION AND CIS-DIAMMINEDICHLOROPLATINUM(II) - A REVIEW OF EXPERIMENTAL AND CLINICAL-DATA [J].
DEWIT, L .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1987, 13 (03) :403-426
[9]
DOUPLE EB, 1978, BRIT J CANCER, V37, P98
[10]
RADIOSENSITIZATION OF HYPOXIC TUMOR-CELLS BY CIS-DICHLORODIAMMINEPLATINUM(II) AND TRANS-DICHLORODIAMMINEPLATINUM(II) [J].
DOUPLE, EB ;
RICHMOND, RC .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1979, 5 (08) :1369-1372