Lm. Berstein et al., ESTROGEN CONTENT AND DNA UNWINDING IN TUMOR AND NORMAL ENDOMETRIAL TISSUE OF AGING ENDOMETRIAL CANCER-PATIENTS, Mutation research, 356(2), 1996, pp. 203-208
Over the past years, data on the role of DNA damage in hormonal carcin
ogenesis have been accumulated. In 21 endometrial cancer (EC) patients
(mean age 61.8+/-1.6 years), no difference between malignant and norm
al endometrium in estradiol content (radioimmunological assay) and in
alkali-induced DNA unwinding as a measure of DNA strand breakage (fluo
rometrical assay) was discovered. At the same time (contrary to normal
endometrium), there were no correlations between the estradiol conten
t in malignant endometrium with DNA unwinding or blood estrogen level.
The estradiol concentration in malignant endometrium increases with a
ge in menopausal EC patients, though no correlation between estrogen c
ontent in endometrial tissue and body weight was discovered. DNA unwin
ding rate in malignant endometrium correlates only with the concentrat
ion of steroid receptors in normal endometrial tissue. It may be possi
ble that before the appearing of any neoplastic changes in the endomet
rium, a higher level of estradiol in the target tissue leads to DNA da
mage which may be considered as a factor predisposing to tumor develop
ment. Practically speaking this would mean that the estradiol content
and DNA unwinding level in endometrial tumors may be used in future as
indicators for therapeutic intervention (first of all, during the hor
mone therapy of EC) and also as markers for the evaluation of the effe
ctiveness of the latter.