Abstract

IntroductionReproductive history has been associated with breast cancer risk, but more knowledge of the underlying biological mechanisms is needed. Because of limited data on normal breast tissue from healthy women, we examined associations of reproductive history and established breast cancer risk factors with breast tissue composition and markers of hormone receptors and proliferation in a nested study within the Karolinska Mammography project for risk prediction for breast cancer (Karma).Materials and methodsTissues from 153 women were obtained by ultrasound-guided core needle biopsy as part of the Karma project. Immunohistochemical staining was used to assessed histological composition of epithelial, stromal and adipose tissue, epithelial and stromal oestrogen receptor (ER) and progesterone receptor (PR) status, and Ki-67 proliferation status. An individualised reproductive score including parity, number of pregnancies without birth, number of births, age at first birth, and duration of breastfeeding, was calculated based on self-reported reproductive history at the time of the Karma study entry. All analyses were adjusted for age and BMI.ResultsCumulated reproductive score was associated with increased total epithelial content and greater expression of epithelial ER. Parity was associated with greater epithelial area, increased epithelial–stromal ratio, greater epithelial ER expression and a lower extent of stromal proliferation. Increasing numbers of pregnancies and births were associated with a greater epithelial area in the entire study set, which remained significant among postmenopausal women. Increasing numbers of pregnancies and births were also associated with a greater expression of epithelial ER among postmenopausal women. Longer duration of breastfeeding was associated with greater epithelial area and greater expression of epithelial PR both in the entire study set and among postmenopausal women. Breastfeeding was also positively associated with greater epithelial ER expression among postmenopausal women. Prior use of oral contraceptives was associated with lower epithelial–stromal ratio amongst all participants and among pre- and postmenopausal women separately.ConclusionReproductive risk factors significantly influence the epithelial tissue compartment and expression of hormone receptors in later life. These changes remain after menopause. This study provides deeper insights of the biological mechanisms by which reproductive history influences epithelial area and expression of hormone receptors, and as a consequence the risk of breast cancer.

Highlights

  • Reproductive history has been associated with breast cancer risk, but more knowledge of the underlying biological mechanisms is needed

  • We examined associations of reproductive history and established breast cancer risk factors with breast tissue composition and markers of hormone receptors and proliferation in a nested study within the Karolinska Mammography project for risk prediction for breast cancer (Karma) [27]

  • Linear regression was used to examine the association between established breast cancer risk factors and reproductive history with epithelial, stromal and adipose tissue measures expressed as percentages of the total area of the section, and percentage expressions of epithelial ER, progesterone receptor (PR) and Ki-67 made from the histological sections

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Summary

Materials and methods

Reproductive history, like parity, age at first birth and number of births, has consistently been shown to be associated with breast cancer risk [1]. The frequency of epithelial cells expressing the proliferation marker Ki-67 has been positively associated with breast cancer risk among premenopausal women [15] It remains inconclusive if parity and reproductive history alter epithelial proliferation [16,17,18]. Linear regression was used to examine the association between established breast cancer risk factors and reproductive history with epithelial, stromal and adipose tissue measures expressed as percentages of the total area of the section, and percentage expressions of epithelial ER, PR and Ki-67 made from the histological sections. All linear regression analyses of epithelial and stromal tissue compartment distributions and epithelial protein expressions were adjusted for age and BMI unless otherwise indicated. Logistic regression was used to examine the association between established breast cancer risk factors and reproductive history with stromal protein expression.

Results
Discussion
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