Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 1994;30(1):7-17.
doi: 10.1007/BF00682737.

The role of aromatase in breast tumors

Affiliations
Review

The role of aromatase in breast tumors

M J Reed. Breast Cancer Res Treat. 1994.

Abstract

Aromatization of androstenedione to estrone in peripheral tissues is the major source of estrogen in postmenopausal women. The aromatase enzyme complex, which mediates the conversion of androstenedione to estrone, is present in several tissues, including adipose tissue and normal and malignant breast tissues. Aromatase activity is detectable in 50-60% of breast tumors, but the contribution that tumor aromatase makes to estrogen concentration in tumors and whether the estrogen formed is biologically important remains a controversial matter. Since concentrations of androstenedione are higher in tumors than in blood, and tumor aromatase activity in vivo may be enhanced by growth factors and by cytokines, the contribution of tumor aromatase to tumor estrogen levels may be higher than suggested by the original calculations. Measurements of tumor aromatase, tumor estrone concentrations, and DNA polymerase alpha activity (a marker of cellular proliferation), in samples obtained before and after treatment with the aromatase inhibitor 4-hydroxyandrostenedione, lend some support to a biological role for estrone formed locally.

PubMed Disclaimer

Similar articles

Cited by

References

    1. J Steroid Biochem Mol Biol. 1993 Mar;44(4-6):589-96 - PubMed
    1. Horm Metab Res. 1986 Sep;18(9):635-7 - PubMed
    1. J Steroid Biochem. 1977 Aug;8(8):893-6 - PubMed
    1. J Clin Oncol. 1992 Mar;10(3):438-46 - PubMed
    1. Eur J Cancer. 1981 Jan;17(1):115-20 - PubMed

MeSH terms

LinkOut - more resources