Return to search

An Analysis of Estrogen Metabolism and Breast Cancer Risk

Breast cancer is the most common noncutaneous form of cancer among women in the US. In recent years, the overall mortality rate has declined, yet there still exists a significant racial disparity in the incidence and mortality between African American and Caucasian women. While numerous hypotheses have been proposed to explain this difference, few offer a biological explanation.
There is a well established association between estrogens and breast cancer risk, and the ratio of two estrogen metabolites, 2-hydroxyestrone (2OHE1) and 16รก-hydroxyestrone (16OHE1), has been implicated as a marker of breast cancer risk.
Many studies have also assessed the relationship between endogenous estrogens and mammographic density. Mammographic density is one of the strongest predictors of breast cancer risk, but the mechanism by which it influences this risk remains unknown. Nonetheless, few have examined mammographic density in relation to the 2OHE1:16OHE1 estrogen metabolite ratio (EMR).
Research suggests that the Cytochrome P450 1B1 (CYP1B1) gene may also mediate breast cancer risk, as this gene is very active in estrogen metabolism. In fact, the Leu432Val polymorphism has reportedly been associated with urinary levels of the 2OHE1:16OHE1 EMR.
The objective of this study was to investigate some of the relationships found among the 2OHE1: 16OHE1 EMR, CYP1B1 Leu432Val polymorphism, mammographic density, race, and breast cancer risk. The 2OHE1:16OHE1 EMR was associated with both breast cancer risk and the CYP1B1 Leu432Val polymorphism, yet, no association with breast cancer risk and this polymorphism was observed. This suggests that if the CYP1B1 Leu432Val polymorphism alters breast cancer risk, it does so through variations in the 2OHE1:16OHE1 EMR. When taking race into account, no association between mammographic density and the 2OHE1:16OHE1 EMR was observed. In culture, evidence was found to suggest that the 2OHE1:16OHE1 EMR is influenced by subcellular effects or other intrinsic factors (i.e. genetic variation), as passage number was the only significant contributor to the 2OHE1:16OHE1 EMR.
The results of this study have great public health significance, as it provides a better understanding of the risk factors, including racial differences, and etiology of breast cancer, which will ultimately lead to better prevention and treatment for all women.

Identiferoai:union.ndltd.org:PITT/oai:PITTETD:etd-04122010-170655
Date28 June 2010
CreatorsLloyd, Stacy Monique
ContributorsEleanor feingold, Robert Ferrell, Emanuela Taioli, Susanne Gollin, Seymour Garte
PublisherUniversity of Pittsburgh
Source SetsUniversity of Pittsburgh
LanguageEnglish
Detected LanguageEnglish
Typetext
Formatapplication/pdf
Sourcehttp://etd.library.pitt.edu/ETD/available/etd-04122010-170655/
Rightsrestricted, I hereby certify that, if appropriate, I have obtained and attached hereto a written permission statement from the owner(s) of each third party copyrighted matter to be included in my thesis, dissertation, or project report, allowing distribution as specified below. I certify that the version I submitted is the same as that approved by my advisory committee. I hereby grant to University of Pittsburgh or its agents the non-exclusive license to archive and make accessible, under the conditions specified below, my thesis, dissertation, or project report in whole or in part in all forms of media, now or hereafter known. I retain all other ownership rights to the copyright of the thesis, dissertation or project report. I also retain the right to use in future works (such as articles or books) all or part of this thesis, dissertation, or project report.

Page generated in 0.0021 seconds