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Associations of stem cell markers CD44, CD24 and ALDH1A1 with mammographic breast density in women with benign breast biopsies.

Authors :
Yaghjyan, Lusine
Heng, Yujing J.
Baker, Gabrielle M.
Murthy, Divya
Mahoney, Matt B.
Rosner, Bernard
Tamimi, Rulla M.
Source :
British Journal of Cancer. Jul2024, Vol. 131 Issue 2, p325-333. 9p.
Publication Year :
2024

Abstract

Background: We examined associations of CD44, CD24 and ALDH1A1 breast stem cell markers with mammographic breast density (MBD), a well-established breast cancer (BCa) risk factor. Methods: We included 218 cancer-free women with biopsy-confirmed benign breast disease within the Nurses' Health Study (NHS) and NHSII. The data on BCa risk factors were obtained from biennial questionnaires. Immunohistochemistry (IHC) was done on tissue microarrays. For each core, the IHC expression was assessed using a semi-automated platform and expressed as percent of positively stained cells for each marker out of the total cell count. MBD was assessed with computer-assisted techniques. Generalised linear regression was used to examine the associations of each marker with square root-transformed percent density (PD), absolute dense and non-dense areas (NDA), adjusted for BCa risk factors. Results: Stromal CD44 and ALDH1A1 expression was positively associated with PD (≥ 10% vs. <10% β = 0.56, 95% confidence interval [CI] [0.06; 1.07] and β = 0.81 [0.27; 1.34], respectively) and inversely associated with NDA (β per 10% increase = −0.17 [−0.34; −0.01] and β for ≥10% vs. <10% = −1.17 [−2.07; −0.28], respectively). Epithelial CD24 expression was inversely associated with PD (β per 10% increase = −0.14 [−0.28; −0.01]. Stromal and epithelial CD24 expression was positively associated with NDA (β per 10% increase = 0.35 [0.2 × 10−2; 0.70] and β per 10% increase = 0.34 [0.11; 0.57], respectively). Conclusion: Expression of stem cell markers is associated with MBD. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00070920
Volume :
131
Issue :
2
Database :
Academic Search Index
Journal :
British Journal of Cancer
Publication Type :
Academic Journal
Accession number :
178589020
Full Text :
https://doi.org/10.1038/s41416-024-02743-2