Moran Olivia, Zaman Tasnim, Eisen Andrea, Demsky Rochelle, Blackmore Kristina, Knight Julia A, Elser Christine, Ginsburg Ophira, Zbuk Kevin, Yaffe Martin, Narod Steven A, Salmena Leonardo, Kotsopoulos Joanne
Women's College Research Institute, Women's College Hospital, 76 Grenville St., 6th Floor, Toronto, ON, M5S 1B2, Canada.
Department of Nutritional Sciences, University of Toronto, Toronto, ON, Canada.
Cancer Causes Control. 2018 Jun;29(6):507-517. doi: 10.1007/s10552-018-1035-y. Epub 2018 Apr 20.
Mammographic density is a risk factor for breast cancer but the mechanism behind this association is unclear. The receptor activator of nuclear factor κB (RANK)/RANK ligand (RANKL) pathway has been implicated in the development of breast cancer. Given the role of RANK signaling in mammary epithelial cell proliferation, we hypothesized this pathway may also be associated with mammographic density. Osteoprotegerin (OPG), a decoy receptor for RANKL, is known to inhibit RANK signaling. Thus, it is of interest to evaluate whether OPG levels modify breast cancer risk through mammographic density.
We quantified serum OPG levels in 57 premenopausal and 43 postmenopausal women using an enzyme-linked immunosorbent assay (ELISA). Cumulus was used to measure percent density, dense area, and non-dense area for each mammographic image. Subjects were classified into high versus low OPG levels based on the median serum OPG level in the entire cohort (115.1 pg/mL). Multivariate models were used to assess the relationship between serum OPG levels and the measures of mammographic density.
Serum OPG levels were not associated with mammographic density among premenopausal women (P ≥ 0.42). Among postmenopausal women, those with low serum OPG levels had higher mean percent mammographic density (20.9% vs. 13.7%; P = 0.04) and mean dense area (23.4 cm vs. 15.2 cm; P = 0.02) compared to those with high serum OPG levels after covariate adjustment.
These findings suggest that low OPG levels may be associated with high mammographic density, particularly in postmenopausal women. Targeting RANK signaling may represent a plausible, non-surgical prevention option for high-risk women with high mammographic density, especially those with low circulating OPG levels.
乳腺钼靶密度是乳腺癌的一个风险因素,但这种关联背后的机制尚不清楚。核因子κB受体激活剂(RANK)/RANK配体(RANKL)通路与乳腺癌的发生有关。鉴于RANK信号在乳腺上皮细胞增殖中的作用,我们推测该通路可能也与乳腺钼靶密度有关。骨保护素(OPG)是RANKL的诱饵受体,已知其可抑制RANK信号。因此,评估OPG水平是否通过乳腺钼靶密度来改变乳腺癌风险具有重要意义。
我们采用酶联免疫吸附测定(ELISA)法对57名绝经前和43名绝经后女性的血清OPG水平进行了定量。使用累积法测量每张乳腺钼靶图像的密度百分比、致密区和非致密区。根据整个队列的血清OPG水平中位数(115.1 pg/mL)将受试者分为OPG水平高和低两组。采用多变量模型评估血清OPG水平与乳腺钼靶密度测量指标之间的关系。
绝经前女性的血清OPG水平与乳腺钼靶密度无关(P≥0.42)。在绝经后女性中,经协变量调整后,血清OPG水平低的女性与血清OPG水平高的女性相比,平均乳腺钼靶密度百分比更高(20.9%对13.7%;P = 0.04),平均致密区更大(23.4 cm对15.2 cm;P = 0.02)。
这些发现表明,低OPG水平可能与高乳腺钼靶密度有关,尤其是在绝经后女性中。针对RANK信号通路可能是乳腺钼靶密度高的高危女性,特别是循环OPG水平低的女性一种可行的非手术预防选择。