Indicators of late normal tissue response after radiotherapy for head and neck cancer:: fibroblasts, lymphocytes, genetics, DNA repair, and chromosome aberrations

被引:90
作者
Borgmann, K
Röper, B
Abd El-Awady, R
Brackrock, S
Bigalke, M
Dörk, T
Alberti, W
Dikomey, E
Dahm-Daphi, J
机构
[1] Univ Hamburg, Hosp Eppendorf, Dept Radiat Oncol, D-20246 Hamburg, Germany
[2] Univ Hamburg, Hosp Eppendorf, Inst Biophys & Radiobiol, D-20246 Hamburg, Germany
[3] Tech Univ Munich, Clin Radiotherapy, D-81675 Munich, Germany
[4] Tech Univ Munich, Clin Radiat Oncol, D-81675 Munich, Germany
[5] Cairo Univ, Natl Canc Inst, Dept Tumor Biol, Cairo, Egypt
[6] Hannover Med Sch, Dept Radiat Oncol, D-30625 Hannover, Germany
[7] Hannover Med Sch, Dept Biochem & Tumour Biol, Clin Obstet & Gynecol, D-30659 Hannover, Germany
关键词
predictive test; radiosensitivity; late tissue response; double-strand break; chromosome aberration; ATM; Nijmegen Breakage Syndrome; ligase IV; RAD50; MRE11;
D O I
10.1016/S0167-8140(02)00167-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To investigate the relationship between late tissue response after radiotherapy, cellular sensitivity and DNA repair capacity measured in dermal fibroblasts and chromosomal aberrations measured in lymphocytes. The study was in particular designed to compare cellular parameters of patients with maximum differences in late tissue reactions. Materials and methods: The study was performed with 16 pair-wise matched head and neck cancer patients 2-7 years after curative therapy exhibiting maximum differences (grade I vs. grade 3) in late normal tissue reactions. Clinical endpoints were fibrosis, telangiectasia. mucositis and xerostomia using the radiation therapy oncology group score. Patients with grade 3 reactions were tested for mutations in ataxia telangiectasia (AT), Nijmegen Breakage Syndrome (NBS), MRE11, RAD50 and DNA ligase IV genes by means of polymerase chain reaction-single-strand conformation polymorphism and sequencing analysis. Skin fibroblasts obtained from biopsies were used to determine the cellular sensitivity by colony formation and the induction and repair of DNA double-strand breaks (dsb) using constant-field gel electrophoresis. Lymphocytes were taken to measure chromosomal damage either in metaphase using conventional chromosome analysis or in Go using premature chromosome condensation (PCC)-technique. Results: Patients with extreme late reactions (grade 3) showed no evidence for an AT, NBS, MRE11 or RAD50 mutation. Studies with fibroblasts revealed that extreme late reactions were associated neither with a pronounced cellular radiosensitivity nor with a difference in dsb repair capacity. In contrast. there was a significant difference in chromosomal damage measured in lymphocytes. After in vitro irradiation with 6 Gy, lymphocytes taken from overreacting patients showed on average a significantly higher number of lethal aberrations than lymphocytes isolated from patients with mild reactions (7.2+/-0.8 vs. 5.0+/-0.3). Similar differences were found for PCC fragments. Conclusion: This study suggests that lymphocytes are more promising than fibroblasts to predict patient's normal tissue response after radiotherapy. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:141 / 152
页数:12
相关论文
共 71 条
[31]   The ATM gene and the radiobiology of ataxia-telangiectasia [J].
Jorgensen, TJ ;
Shiloh, Y .
INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, 1996, 69 (05) :527-537
[32]   Quantification of late complications after radiation therapy [J].
Jung, H ;
Beck-Bornholdt, HP ;
Svoboda, V ;
Alberti, W ;
Herrmann, N .
RADIOTHERAPY AND ONCOLOGY, 2001, 61 (03) :233-246
[33]   Ku70/80 gene expression and DNA-dependent protein kinase (DNA-PK) activity do not correlate with double-strand break (dsb) repair capacity and cellular radiosensitivity in normal human fibroblasts [J].
Kasten, U ;
Plottner, N ;
Johansen, J ;
Overgaard, J ;
Dikomey, E .
BRITISH JOURNAL OF CANCER, 1999, 79 (7-8) :1037-1041
[34]   A correlation between residual radiation-induced DNA double-strand breaks in cultured fibroblasts and late radiotherapy reactions in breast cancer patients [J].
Kiltie, AE ;
Ryan, AJ ;
Swindell, R ;
Barber, JBP ;
West, CML ;
Magee, B ;
Hendry, JH .
RADIOTHERAPY AND ONCOLOGY, 1999, 51 (01) :55-65
[35]  
Kondrashova TV, 1997, ENVIRON HEALTH PERSP, V105, P1437
[36]   ABSENCE OF CORRELATIONS BETWEEN RADIOSENSITIVITIES OF HUMAN LYMPHOCYTES-T IN G0 AND SKIN FIBROBLASTS IN LOG PHASE [J].
KUSHIRO, J ;
NAKAMURA, N ;
KYOIZUMI, S ;
NISHIKI, M ;
DOHI, K ;
AKIYAMA, M .
RADIATION RESEARCH, 1990, 122 (03) :326-332
[37]   ABSENCE OF P350 SUBUNIT OF DNA-ACTIVATED PROTEIN-KINASE FROM A RADIOSENSITIVE HUMAN CELL-LINE [J].
LEESMILLER, SP ;
GODBOUT, R ;
CHAN, DW ;
WEINFELD, M ;
DAY, RS ;
BARRON, GM ;
ALLALUNISTURNER, J .
SCIENCE, 1995, 267 (5201) :1183-1185
[38]   INVITRO RADIOSENSITIVITY OF HUMAN-DIPLOID FIBROBLASTS DERIVED FROM WOMEN WITH UNUSUALLY SENSITIVE CLINICAL-RESPONSES TO DEFINITIVE RADIATION-THERAPY FOR BREAST-CANCER [J].
LOEFFLER, JS ;
HARRIS, JR ;
DAHLBERG, WK ;
LITTLE, JB .
RADIATION RESEARCH, 1990, 121 (02) :227-231
[39]   The modelled benefits of individualizing radiotherapy patients' dose using cellular radiosensitivity assays with inherent variability [J].
Mackay, RI ;
Hendry, JH .
RADIOTHERAPY AND ONCOLOGY, 1999, 50 (01) :67-75
[40]   Normal cellular radiosensitivity in an adult Fanconi anaemia patient with marked clinical radiosensitivity [J].
Marcou, Y ;
D'Andrea, A ;
Jeggo, PA ;
Plowman, PN .
RADIOTHERAPY AND ONCOLOGY, 2001, 60 (01) :75-79