Breast cancer and steroid metabolizing enzymes: The role of progestogens

被引:16
|
作者
Pasqualini, Jorge R. [1 ]
机构
[1] Hormones & Canc Res Unit, F-75014 Paris, France
关键词
Breast cancer; Progestogen; Enzymes; Dydrogesterone; Progesterone; ESTROGEN SULFOTRANSFERASE ACTIVITY; HORMONE-DEPENDENT MCF-7; CELL-LINES; PROGESTERONE METABOLITES; NOMEGESTROL ACETATE; PROMEGESTONE R-5020; SULFATASE ACTIVITY; PROLIFERATION; ESTRADIOL; 20-ALPHA-DIHYDROPROGESTERONE;
D O I
10.1016/j.maturitas.2009.11.006
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
It is well documented that breast tissue, both normal and cancerous, contains all the enzymatic systems necessary for the bioformation and metabolic transformation of estrogens, androgens and progesterone. These include sulfatases, aromatase, hydroxysteroid-dehydrogenases, sulfotransferases, hydroxylases and glucuronidases. The control of these enzymes plays an important role in the development and pathogenesis of hormone-dependent breast cancer. As discussed in this review, various progestogens including dydrogesterone and its 20 alpha-dihydro-derivative, medrogestone, promegestone, nomegestrol acetate and norelgestromin can reduce intratissular levels of estradiol in breast cancer by blocking sulfatase and 17 beta-hydroxysteroid-dehydrogenase type 1 activities. A possible correlation has been postulated between breast cell proliferation and estrogen sulfotransferase activity. Progesterone is largely transformed in the breast; normal breast produces mainly 4-ene derivatives, whereas 5 alpha-derivatives are most common in breast cancer tissue. It has been suggested that this specific conversion of progesterone may be involved in breast carcinogenesis. In conclusion, treatment with anti-aromatases combined with anti-sulfatase or 17 beta-hydroxysteroid-dehydrogenase type 1 could provide new therapeutic possibilities in the treatment of patients with hormone-dependent breast cancer. (C) 2009 Elsevier Ireland Ltd. All rights reserved
引用
收藏
页码:S17 / S21
页数:5
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