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Review
. 2005 Jul;96(2):95-108.
doi: 10.1016/j.jsbmb.2005.02.014.

Progestins and progesterone in hormone replacement therapy and the risk of breast cancer

Affiliations
Review

Progestins and progesterone in hormone replacement therapy and the risk of breast cancer

Carlo Campagnoli et al. J Steroid Biochem Mol Biol. 2005 Jul.

Abstract

Controlled studies and most observational studies published over the last 5 years suggest that the addition of synthetic progestins to estrogen in hormone replacement therapy (HRT), particularly in continuous-combined regimen, increases the breast cancer (BC) risk compared to estrogen alone. By contrast, a recent study suggests that the addition of natural progesterone in cyclic regimens does not affect BC risk. This finding is consistent with in vivo data suggesting that progesterone does not have a detrimental effect on breast tissue. The increased BC risk found with the addition of synthetic progestins to estrogen could be due to the regimen and/or the kind of progestin used. Continuous-combined regimen inhibits the sloughing of mammary epithelium that occurs after progesterone withdrawal in a cyclic regimen. More importantly, the progestins used (medroxyprogesterone acetate and 19-Nortestosterone-derivatives) are endowed with some non-progesterone-like effects, which can potentiate the proliferative action of estrogens. Particularly relevant seem to be the metabolic and hepatocellular effects (decreased insulin sensitivity, increased levels and activity of insulin-like growth factor-I, and decreased levels of SHBG), which contrast the opposite effects induced by oral estrogen.

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Figures

Fig. 1
Fig. 1
Relative risks associated with use of different hormones by women with incident HRT exposure, compared with non-users: E3N-EPIC study [26]. TD-E2 = transdermal estradiol.
Fig. 2
Fig. 2
Relative risk of premenopausal breast cancer in women with regular menses according to mid-luteal progesterone levels (40 cases and 108 matched control subjects from the ORDET cohort of 5963 premenopausal women) [6].
Fig. 3
Fig. 3
Relative risk (RR) or odd ratios (OR) of breast cancer in long term HRT users. (•) significant difference from nonusers; ( formula image) mainly medroxyprogesterone acetate (MPA); ( formula image) 19-Nortestosterone-derived progestins and (20%) MPA; (*) only 19-Nortestosterone-derived progestins; (▴) mainly 19-Nortestosterone-derived progestins.
Fig. 4
Fig. 4
Progestins used in HRT in different countries.

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References

    1. Clemmesen J. Statistical studies in the aetiology of malignant neoplasms, 3. Acta Pathol Microbiol Scand. 1969;209(S1):S1–S58. - PubMed
    1. Trichopoulos D, MacMahon B, Cole P. Menopause and breast cancer risk. J Natl Cancer Inst. 1972;48(3):605–613. - PubMed
    1. Early Breast Cancer Trialists’ Collaborative Group. Tamoxifen for early breast cancer: an overview of the randomised trials. Lancet. 1998;351(9114):1451–1467. - PubMed
    1. Endogenous sex hormones and breast cancer in postmenopausal women: reanalysis of nine prospective studies. J Natl Cancer Inst. 2002;94(8):606–616. - PubMed
    1. Travis RC, Key TJ. Oestrogen exposure and breast cancer risk. Breast Cancer Res. 2003;5(5):239–247. - PMC - PubMed

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