Associations of stem cell markers in benign breast tissue with subsequent breast cancer risk.

Benign breast disease breast cancer risk stem cell markers

Journal

American journal of cancer research
ISSN: 2156-6976
Titre abrégé: Am J Cancer Res
Pays: United States
ID NLM: 101549944

Informations de publication

Date de publication:
2023
Historique:
received: 06 09 2023
accepted: 06 11 2023
medline: 8 1 2024
pubmed: 8 1 2024
entrez: 8 1 2024
Statut: epublish

Résumé

We examined associations of stem cell markers CD44, CD24, and ALDH1A1 in benign breast biopsy samples with subsequent breast cancer (BCa) risk and explored if these associations were mediated by mammographic breast density (MBD). We included 101 BCa cases/375 controls, all with previous biopsy-confirmed benign breast disease (BBD) within the Nurses' Health Study (NHS) and NHSII. The data on BCa risk factors were obtained from biennial questionnaires. MBD was assessed with computer-assisted techniques. Immunohistochemistry (IHC) was done on BBD tissue microarrays. For each core, the IHC expression was assessed using a semi-automated method, and expressed as % of cells that stained positive for a specific marker out of the total cell count. Logistic regression was used to examine the associations of each marker's expression of each (in epithelium and stroma) with BCa risk, adjusted for risk factors. Stromal CD44 expression was inversely associated with BCa risk (OR for ≥10% vs. <10%=0.58, 95% CI 0.34, 1.00). Combined stromal + epithelial CD24 expression was inversely associated with BCa risk (>50% vs. 0-10% OR=0.17, 95% CI 0.04-0.81, p-trend =0.03). Stromal CD24 and ALDH1A1 as well as epithelial expression of any of the three markers were not associated with BCa risk. In a smaller subset of women with available MBD, these observed associations did not appear to be mediated by MBD. Our findings suggest inverse associations of CD44 in stroma and combined stromal + epithelial CD24 with BCa risk. Future studies are warranted to confirm our findings and to examine these associations by BBD subtype.

Identifiants

pubmed: 38187066
pmc: PMC10767353

Types de publication

Journal Article

Langues

eng

Pagination

6280-6289

Informations de copyright

AJCR Copyright © 2023.

Déclaration de conflit d'intérêts

None.

Auteurs

Lusine Yaghjyan (L)

Department of Epidemiology, College of Public Health and Health Professions and College of Medicine, University of Florida Gainesville, FL, USA.

Yujing J Heng (YJ)

Department of Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School Boston, MA, USA.

Gabrielle M Baker (GM)

Department of Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School Boston, MA, USA.

Divya Murthy (D)

Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School Boston, MA, USA.

Matt B Mahoney (MB)

Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School Boston, MA, USA.

Bernard Rosner (B)

Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School Boston, MA, USA.

Rulla M Tamimi (RM)

Department of Population Health Sciences, Weill Cornell Medicine New York, NY, USA.

Classifications MeSH