TY - JOUR
T1 - Abnormal oxidative metabolism of estradiol in women with breast cancer
AU - Schneider, J.
AU - Kinne, D.
AU - Fracchia, A.
AU - Pierce, V.
AU - Anderson, K. E.
AU - Bradlow, H. L.
AU - Fishman, J.
PY - 1982
Y1 - 1982
N2 - The three dominant oxidative biotransformations of estradiol were examined in 10 normal women and 33 females with breast cancer by using a recently devised radiometric method. Estradiol tracers, labeled with 3H specifically in the 17α, C-2, or 16α position, were used to measure both the rate and extent of 17β-ol oxidation (the initial metabolic step) and the subsequent 2- and 16α-oxidative reactions. The mean ± SEM values for the extent of estradiol metabolism at these three specific sites were 76.9 ± 5.3%, 31.1 ± 4.0%, and 9.3 ± 0.8%, respectively, in normal subjects. Corresponding data in patients with breast cancer - i.e., 73.0 ± 4.2%, 32.7 ± 2.7%, and 14.9 ± 1.5% - revealed a significantly greater extent of 16α-hydroxylation in the latter population. Because the 16α-hydroxylated compounds (including estriol) are themseleves potent estrogens, these changes may have important hyperestrogenic consequences that could have a bearing on the etiology of the disease.
AB - The three dominant oxidative biotransformations of estradiol were examined in 10 normal women and 33 females with breast cancer by using a recently devised radiometric method. Estradiol tracers, labeled with 3H specifically in the 17α, C-2, or 16α position, were used to measure both the rate and extent of 17β-ol oxidation (the initial metabolic step) and the subsequent 2- and 16α-oxidative reactions. The mean ± SEM values for the extent of estradiol metabolism at these three specific sites were 76.9 ± 5.3%, 31.1 ± 4.0%, and 9.3 ± 0.8%, respectively, in normal subjects. Corresponding data in patients with breast cancer - i.e., 73.0 ± 4.2%, 32.7 ± 2.7%, and 14.9 ± 1.5% - revealed a significantly greater extent of 16α-hydroxylation in the latter population. Because the 16α-hydroxylated compounds (including estriol) are themseleves potent estrogens, these changes may have important hyperestrogenic consequences that could have a bearing on the etiology of the disease.
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U2 - 10.1073/pnas.79.9.3047
DO - 10.1073/pnas.79.9.3047
M3 - Article
C2 - 6953448
AN - SCOPUS:0000240689
SN - 0027-8424
VL - 79
SP - 3047
EP - 3051
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 9 I
ER -