Background: Side effects of radiotherapy in normal tissue is determine
d by a variety of factors of which cellular and genetic contributions
are described here. Material and Methods: Review. Results: Normal tiss
ue damage after irradiation is largely due to loss of cellular prolife
rative capacity. This can be due to mitotic cell death, apoptosis, or
terminal differentiation. Dead or differentiated cells release cytokin
es which additionally modulate the tissue response. DNA damage, in par
ticular non-reparable or misrepaired double-strand breaks are consider
ed the basic lesion leading to G1-arrest and ultimately to cell. inact
ivation. Conclusion: Evidence for genetic bases of normal tissue respo
nse, cell killing and DNA-repair capacity is presented. However, a dir
ect link of all 3 endpoints has not yet been proved directly.