TY - JOUR
T1 - Genetic variation in normal tissue toxicity induced by ionizing radiation
AU - Popanda, Odilia
AU - Marquardt, Jens Uwe
AU - Chang-Claude, Jenny
AU - Schmezer, Peter
N1 - Funding Information:
We wish to thank P. Waas and W. Popanda (Division of Toxicology and Cancer Risk Factor, German Cancer Research Center) for their excellent technical assistance, R. Haselmann (Department of Clinical Radiology, University Hospital Heidelberg,) and K. Smit and S. Behrens (Cancer Epidemiology, German Cancer Research Center) for their important contribution to blood sampling and data collection. We are grateful to all patients who participated in the study. This work was partially supported by the German ‘Bundesamt für Strahlenschutz’, Salzgitter, Project StSch. 4212 and StSch. 4405.
PY - 2009/7/10
Y1 - 2009/7/10
N2 - Radiotherapy is an important weapon in the treatment of cancer, but adverse reactions developing in the co-irradiated normal tissue can be a threat for patients. Early reactions might disturb the usual application schedule and limit the radiation dose. Late appearing and degenerative reactions might reduce or destroy normal tissue function. Genetic markers conferring the ability to identify hyper-sensitive patients in advance would considerably improve therapy. Association studies on genetic variation and occurrence of side effects should help to identify such markers. This survey includes published studies and novel data from our own laboratory. It illustrates the presence of candidate polymorphisms in genes involved in the cellular response to irradiation which could be used as predictive markers for radiosensitivity in breast or prostate cancer patients. For other tumor types such as head and neck cancers or brain tumors, the available data are much more limited. In any case, further validation of these markers is needed in large patient cohorts with systematically recorded data on side effects and patient characteristics. Genetic variation contributing to radiosensitivity should be screened on a broader basis using newly developed, more comprehensive approaches such as genome-wide association studies.
AB - Radiotherapy is an important weapon in the treatment of cancer, but adverse reactions developing in the co-irradiated normal tissue can be a threat for patients. Early reactions might disturb the usual application schedule and limit the radiation dose. Late appearing and degenerative reactions might reduce or destroy normal tissue function. Genetic markers conferring the ability to identify hyper-sensitive patients in advance would considerably improve therapy. Association studies on genetic variation and occurrence of side effects should help to identify such markers. This survey includes published studies and novel data from our own laboratory. It illustrates the presence of candidate polymorphisms in genes involved in the cellular response to irradiation which could be used as predictive markers for radiosensitivity in breast or prostate cancer patients. For other tumor types such as head and neck cancers or brain tumors, the available data are much more limited. In any case, further validation of these markers is needed in large patient cohorts with systematically recorded data on side effects and patient characteristics. Genetic variation contributing to radiosensitivity should be screened on a broader basis using newly developed, more comprehensive approaches such as genome-wide association studies.
UR - http://www.scopus.com/inward/record.url?scp=67649198795&partnerID=8YFLogxK
U2 - 10.1016/j.mrfmmm.2008.10.014
DO - 10.1016/j.mrfmmm.2008.10.014
M3 - Journal articles
C2 - 19022265
AN - SCOPUS:67649198795
SN - 0027-5107
VL - 667
SP - 58
EP - 69
JO - Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis
JF - Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis
IS - 1-2
ER -