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Exploring Breast Cancer Estrogen Disposition: The Basis for Endocrine Manipulation

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CLINICAL CANCER RESEARCH
卷 17, 期 15, 页码 4948-4958

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AMER ASSOC CANCER RESEARCH
DOI: 10.1158/1078-0432.CCR-11-0043

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  1. Norwegian Cancer Society
  2. Western Health Region of Norway
  3. Innovest Program of Excellence
  4. Breast Cancer Research Foundation
  5. Mary-Jean Mitchell Green Foundation
  6. Breakthrough Breast Cancer
  7. National Institute for Health Research

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Although normal breast tissue and breast cancer estrogens are known to be elevated compared with plasma estrogen levels, the mechanism behind this phenomenon has been an issue of debate for 2 decades. If local estrogen aromatization were to be confirmed as the main estrogen source in breast cancer tissue, tissue-specific inhibition of estrogen production, avoiding systemic side effects, would become a potentially attractive option for breast cancer treatment and prevention. Based on recent results from our groups exploring tissue estrogens, together with estrogen-synthesizing and estrogen-regulated gene expression levels, we propose a new model to explain elevated breast tissue estrogen levels. Although local estrogen production may be important, the local contribution is overruled by rapid plasma-to-tissue equilibration, including active uptake of circulating estrogens or enhanced tissue binding. As for breast cancer tissue levels, elevated levels of estradiol may be explained to a large extent by estrogen receptor binding and local conversion of estrone into estradiol. This model indicates that effective suppression of benign and malignant tissue estrogens as a treatment for ER+ breast cancer requires systemic suppression and will not be markedly affected by local enzyme targeting. Clin Cancer Res; 17(15); 4948-58. (C)2011 AACR.

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