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Carcinogenesis, Vol. 24, No. 4, 697-702, April 2003
© 2003 Oxford University Press


MOLECULAR EPIDEMIOLOGY AND CANCER PREVENTION

Relative imbalances in estrogen metabolism and conjugation in breast tissue of women with carcinoma: potential biomarkers of susceptibility to cancer

Eleanor G. Rogan1,6, Alaa F. Badawi2, Prabu D. Devanesan1, Jane L. Meza3, James A. Edney4, William W. West5, Sheila M. Higginbotham1 and Ercole L. Cavalieri1

1 Eppley Institute for Research in Cancer and Allied Diseases, University of Nebraska Medical Center, 986805 Nebraska Medical Center, Omaha, Ne 68198-6805
2 Division of Population Sciences, Fox Chase Cancer Center, 7701 Burholme Avenue, Philadelphia, Pa 19111
3 Department of Preventive and Societal Medicine, University of Nebraska Medical Center, 984350 Nebraska Medical Center, Omaha, Ne 68198-4350
4 Department of Surgery, University of Nebraska Medical Center, 983280 Nebraska Medical Center, Omaha, NE 68198-3280
5 Department of Pathology and Microbiology, University of Nebraska Medical Center, 987549 Nebraska Medical Center, Omaha, NE 68198-7549, USA

6 To whom correspondence should be addressed Email: egrogan{at}unmc.edu

Exposure to estrogens has been associated with an increased risk of developing breast cancer. Breast biopsy tissues from 49 women without breast cancer (controls) and 28 with breast carcinoma (cases) were analyzed by HPLC with electrochemical detection for 31 estrogen metabolites and catechol estrogen quinone–glutathione conjugates. The levels of estrone and estradiol were higher in cases. More 2-catechol estrogen (CE) than 4-CE was observed in controls, but the 4-CE were three times higher than 2-CE in cases. In addition, the 4-CE were nearly four times higher in cases than in controls. Less O-methylation was observed for the CE in cases. The level of catechol estrogen quinone conjugates in cases was three times that in controls, suggesting in the cases a higher probability for the quinones to react with DNA and generate mutations that may initiate cancer. The levels of 4-CE and quinone conjugates were highly significant predictors of breast cancer. These results suggest that some catechol estrogen metabolites and conjugates could serve as biomarkers to predict risk of breast cancer.


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