Abstract
Abstract Background The insulin-like growth factor (IGF) pathway is implicated in a naturally occurring process of tissue remodeling during which cells acquire stem cell-like characteristics. We examined associations of circulating IGF-1 and IGF binding protein-3 (IGFBP-3) with expression of CD44, CD24, and ALDH1A1 stem cell markers in benign breast biopsies. Methods This study included 151 cancer-free women with incident biopsy-confirmed benign breast disease and blood samples within the Nurses’ Health Study II. The data on reproductive and other BCa risk factors were obtained from biennial questionnaires. Immunohistochemistry (IHC) was done on tissue microarrays. For each core, the IHC expression was assessed using QuPath, and expressed as % of cells that stain positively for a specific marker out of the total cell count. Generalized linear regression was used to examine the associations of plasma IGF-I and IGFBP-3 (continuous log-transformed and quartiles) with log-transformed expression of each marker (in epithelium and stroma), adjusted for BCa risk factors. Results In multivariate analysis, continuous circulating IGF-1 and IGFBP-3 measures were not associated with the continuous expression of any of the markers in the epithelium or stroma. Women whose IGFBP-3 levels were in the top quartile appeared to have lower expression of stromal CD24 compared to those in the lowest quartile (β = − 0.38, 95% CI − 0.69, − 0.08, p-trend = 0.06). Conclusions Higher circulating IGFBP-3 levels were associated with lower stromal CD24 expression in benign breast tissue. Our findings provide indirect evidence of the inducing effect of IGF pathway on epithelial-to-mesenchymal transitions and stem cell activity in the breast.
Highlights
The insulin-like growth factor (IGF) pathway is implicated in a naturally occurring process of tissue remodeling during which cells acquire stem cell-like characteristics
In multivariate analysis, continuous circulating IGF-1 and IGF binding protein-3 (IGFBP-3) measures were not associated with the continuous expression of any of the markers in the epithelium or stroma
Higher circulating IGFBP-3 levels were associated with lower stromal CD24 expression in benign breast tissue
Summary
The insulin-like growth factor (IGF) pathway is implicated in a naturally occurring process of tissue remodeling during which cells acquire stem cell-like characteristics. Epidemiologic and animal studies suggest an increase in breast cancer risk with elevated circulating IGF-1 and insulin-like growth factor-binding protein 3 (IGFBP-3) which are associated with a number of breast cancer risk factors, including birthweight, mammographic density, benign breast disease (BBD) as well as BBD to tumor progression [5–11]. Accumulating reports show that breast cancer stem cells with co-stained C D44+/CD24− or CD44+/ CD24low and ALDH1+ or ALDH1high are responsible for tumor initiation, progression, metastasis, and drug resistance [16–24]. In line with this evidence, we hypothesized that higher levels of IGF-1 and IGFBP-3 would be positively associated with the expression of CD44 and ALDH1A1, and inversely associated with CD24 (consistent with associations of CD44high, ALDH1A1high, and CD24low with unfavorable tumor features)
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