Women's College Research Institute, Women's College Hospital, Toronto, Ontario, Canada.
Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.
Cancer Epidemiol Biomarkers Prev. 2020 Jun;29(6):1264-1270. doi: 10.1158/1055-9965.EPI-19-1154. Epub 2020 Apr 10.
Emerging evidence supports a role of the receptor activator of NF-κB (RANK) pathway in normal mammary gland development and breast carcinogenesis. Osteoprotegerin (OPG) is the endogenous decoy receptor for RANK-ligand (RANKL), which inhibits RANK-signaling. Whether OPG may be a biomarker of breast cancer risk remains unclear.
We evaluated the association between plasma OPG and breast cancer risk in a case ( = 297)-control ( = 297) study nested within the Nurses' Health Study II. Cases were women who were cancer-free and premenopausal at blood collection who developed invasive breast cancer. OPG was quantified using an ELISA. Conditional logistic regression was used to estimate multivariable odds ratios (OR) and 95% confidence intervals (CI) for the association between OPG levels and breast cancer risk, adjusting for potential confounders. Unconditional logistic regression, additionally adjusting for matching factors, was used for stratified analyses.
Overall, there was no substantial evidence for an association between plasma OPG levels and breast cancer risk, although the point estimate for the highest (vs. lowest) quartile was below 1 (OR = 0.78; 95% CI, 0.46-1.33; = 0.30). There was no evidence of heterogeneity by various reproductive, hormonal, or tumor characteristics, including hormone receptor status and grade (all ≥ 0.17).
Findings from this prospective study do not provide substantial evidence for an association between circulating OPG and breast cancer risk among premenopausal women; however, we were underpowered in stratified analyses.
Results do not provide strong evidence for OPG as a potential biomarker of breast cancer risk among premenopausal women.
新出现的证据支持核因子-κB(NF-κB)受体激活剂(RANK)通路在正常乳腺发育和乳腺癌发生中的作用。护骨素(OPG)是 RANK 配体(RANKL)的内源性诱饵受体,可抑制 RANK 信号。OPG 是否可能成为乳腺癌风险的生物标志物仍不清楚。
我们在护士健康研究 II 中进行了一项病例对照研究(病例=297,对照=297),评估了血浆 OPG 与乳腺癌风险之间的关系。病例为采血时无癌症且绝经前的女性,且患有浸润性乳腺癌。使用 ELISA 定量检测 OPG。采用条件逻辑回归估计 OPG 水平与乳腺癌风险之间的多变量比值比(OR)和 95%置信区间(CI),并调整潜在混杂因素。采用非条件逻辑回归,另外调整匹配因素,进行分层分析。
总体而言,血浆 OPG 水平与乳腺癌风险之间没有明显的关联,尽管最高(vs.最低)四分位数的点估计值低于 1(OR=0.78;95%CI,0.46-1.33;=0.30)。根据各种生殖、激素或肿瘤特征,包括激素受体状态和分级,没有发现异质性(均≥0.17)。
这项前瞻性研究的结果并未提供实质性证据表明循环 OPG 与绝经前妇女乳腺癌风险之间存在关联;然而,我们在分层分析中能力不足。
结果并未为 OPG 作为绝经前妇女乳腺癌风险潜在生物标志物提供有力证据。