The extreme radiosensitivity of the squamous cell carcinoma SKX is due to a defect in double-strand break repair

被引:42
作者
Kasten-Pisula, Ulla
Menegakis, Apostolos [2 ,4 ]
Brammer, Ingo
Borgmann, Kerstin
Mansour, Wael Y.
Degenhardt, Sarah
Krause, Mechthild [2 ,4 ]
Schreiber, Andreas [2 ,5 ]
Dahm-Daphi, Jochen
Petersen, Cordula [2 ]
Dikomey, Ekkehard [1 ]
Baumann, Michael [2 ,3 ,4 ]
机构
[1] Univ Med Ctr Hamburg Eppendorf, Dept Radiotherapy & Radiooncol, Lab Radiobiol & Expt Radiooncol, D-20246 Hamburg, Germany
[2] Tech Univ Dresden, Med Fac Carl Gustav Carus, Ctr Radiat Res Oncol, Dept Radiat Oncol, Dresden, Germany
[3] Tech Univ Dresden, Med Fac Carl Gustav Carus, Ctr Radiat Res Oncol, Expt Ctr, Dresden, Germany
[4] Tech Univ Dresden, Med Fac Carl Gustav Carus, OncoRay Ctr Radiat Res Oncol, Dresden, Germany
[5] Stadt Krankenhaus Dresden Friedrichstadt, Dept & Practice Radiotherapy, Dresden, Germany
关键词
Squamous cell carcinoma; Tumour radiosensitivity; Double-strand breaks; Repair; Prediction; SPONTANEOUS APOPTOSIS; RADIATION; P53; EXPRESSION; MECHANISMS; SURVIVAL; RADIOCHEMOTHERAPY; RADIOTHERAPY; DEFICIENT; MUTATIONS;
D O I
10.1016/j.radonc.2008.10.019
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Squamous cell carcinomas (SCCs) are characterized by moderate radiosensitivity. We have established the human head & neck SCC cell line SKX which shows an exceptionally high radiosensitivity. It was the aim of this study to understand the underlying mechanisms. Materials & methods: Experiments were performed with SKX and FaDu, the latter taken as a control of moderate radiosensitivity. Cell lines were grown as xenografts as well as cell Cultures. For xenografts, radiosensitivity was determined via local tumour control assay, and for cell Cultures using colony assay. For cell Cultures, apoptosis was determined by Annexin V staining and G1-arrest by BrdU labelling. Double-strand breaks (DSBs) were detected by both constant-field gel electrophoresis (CFGE) and gamma H2AX-foci technique; DSB rejoining was also assessed by in vitro rejoining assay; chromosomal damage was determined by G01-assay. Results: Compared to FaDu, SKX cells are extremely radiosensitive as found for both xenografts (TCD50 for 10 fractions 46.0 Gy [95% C.I.: 39; 54 Gy] vs. 18.9 Gy [95% C.I.: 13; 25 Gy]) and cell cultures (D-0.01: 7.1 vs. 3.5 Gy). Both cell lines showed neither radiation-induced apoptosis nor radiation-induced permanent G1 arrest. For DSBs, there was no difference in the induction but for repair with SKX cells showing a higher level of both, slowly repaired DSBs and residual DSBs. The in vitro DSB repair assay revealed that SKX cells are defective in nonhomologous endjoining (NHEJ), and that More than 40% of DSBs are rejoined by single-strand annealing (SSA). SKX cells also depicted a two-fold higher number of lethal chromosomal aberrations when compared to FaDu cells. Conclusions: The extreme radiosensitivity of the SCC SKX seen both in vivo and in vitro can be ascribed to a reduced DNA double-strand break repair, resulting from a defect in NHEJ. This defect might be due to preferred usage of other pathways, such as SSA, which prevents efficient endjoining. (C) 2008 Elsevier Ireland Ltd. All rights reserved. Radiotherapy and Oncology 90 (2009) 257-264
引用
收藏
页码:257 / 264
页数:8
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