Residual γH2AX foci after ex vivo irradiation of patient samples with known tumour-type specific differences in radio-responsiveness

被引:31
作者
Menegakis, Apostolos [1 ,2 ,3 ,4 ]
De Colle, Chiara [5 ]
Yaromina, Ala [6 ]
Hennenlotter, Joerg [7 ]
Stenzl, Arnulf [7 ]
Scharpf, Marcus [8 ]
Fend, Falko [8 ]
Noell, Susan [9 ]
Tatagiba, Marcos [9 ]
Brucker, Sara [2 ,10 ]
Wallwiener, Diethelm [2 ,10 ]
Boeke, Simon [1 ,2 ,3 ,4 ]
Ricardi, Umberto [5 ]
Baumann, Michael [3 ,4 ,11 ,12 ,13 ,14 ,15 ]
Zips, Daniel [1 ,2 ,3 ,4 ]
机构
[1] Univ Tubingen, Fac Med, Dept Radiat Oncol, Tubingen, Germany
[2] Univ Tubingen, Univ Hosp, Tubingen, Germany
[3] German Canc Res Ctr, Heidelberg, Germany
[4] German Consortium Translat Canc Res DKTK Partner, Tubingen, Germany
[5] Univ Turin, Radiat Oncol, Dept Oncol, I-10124 Turin, Italy
[6] Maastricht Univ, Med Ctr, GROW Sch Oncol & Dev Biol, Dept Radiat Oncol Maastro, NL-6200 MD Maastricht, Netherlands
[7] Univ Tubingen, Dept Urol, Tubingen, Germany
[8] Univ Tubingen, Dept Pathol, Tubingen, Germany
[9] Univ Tubingen, Dept Neurosurg, Tubingen, Germany
[10] Univ Tubingen, Dept & Res Inst Womens Hlth, Fac Med, Tubingen, Germany
[11] Tech Univ, Fac Med, Dept Radiat Oncol, Tubingen, Germany
[12] Tech Univ, Univ Hosp Carl Gustav Carus, Tubingen, Germany
[13] Tech Univ Dresden, Fac Med, OncoRay Natl Ctr Radiat Res Oncol, Dresden, Germany
[14] Tech Univ Dresden, Univ Hosp Carl Gustav Carus, Dresden, Germany
[15] Helmholtz Zentrum Dresden Rossendorf, Dresden, Germany
关键词
gamma H2AX foci; Radiotherapy; DNA repair; Tumour specimens; Intrinsic radiation sensitivity; Personalized radiation oncology; DOUBLE-STRAND BREAKS; DNA-DAMAGE; CELLULAR RADIOSENSITIVITY; HISTONE H2AX; INTRINSIC RADIOSENSITIVITY; RADIATION-THERAPY; REPAIR; RADIOTHERAPY; SURVIVAL; ASSAY;
D O I
10.1016/j.radonc.2015.08.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To apply our previously published residual ex vivo gamma H2AX foci method to patient-derived tumour specimens covering a spectrum of tumour-types with known differences in radiation response. In addition, the data were used to simulate different experimental scenarios to simplify the method. Materials and methods: Evaluation of residual gamma H2AX foci in well-oxygenated tumour areas of ex vivo irradiated patient-derived tumour specimens with graded single doses was performed. Immediately after surgical resection, the samples were cultivated for 24 h in culture medium prior to irradiation and fixed 24 h post-irradiation for gamma H2AX foci evaluation. Specimens from a total of 25 patients (including 7 previously published) with 10 different tumour types were included. Results: Linear dose response of residual gamma H2AX foci was observed in all specimens with highly variable slopes among different tumour types ranging from 0.69 (95% CI: 1.14-0.24) to 3.26 (95% Cl: 4.13-2.62) for chondrosarcomas (radioresistant) and classical seminomas (radiosensitive) respectively. Simulations suggest that omitting dose levels might simplify the assay without compromising robustness. Conclusion: Here we confirm clinical feasibility of the assay. The slopes of the residual foci number are well in line with the expected differences in radio-responsiveness of different tumour types implying that intrinsic radiation sensitivity contributes to tumour radiation response. Thus, this assay has a promising potential for individualized radiation therapy and prospective validation is warranted. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:480 / 485
页数:6
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