Overexpression of Estrogen Receptor α in Mammary Glands of Aging Mice Is Associated with a Proliferative Risk Signature and Generation of Estrogen Receptor α-Positive Mammary Adenocarcinomas.


Journal

The American journal of pathology
ISSN: 1525-2191
Titre abrégé: Am J Pathol
Pays: United States
ID NLM: 0370502

Informations de publication

Date de publication:
01 2023
Historique:
received: 28 06 2022
revised: 29 08 2022
accepted: 28 09 2022
pmc-release: 01 01 2024
pubmed: 5 12 2022
medline: 20 12 2022
entrez: 4 12 2022
Statut: ppublish

Résumé

Age is a risk factor for human estrogen receptor-positive breast cancer, with highest prevalence following menopause. While transcriptome risk profiling is available for human breast cancers, it is not yet developed for prognostication for primary or secondary breast cancer development utilizing at-risk breast tissue. Both estrogen receptor α (ER) and aromatase overexpression have been linked to human breast cancer. Herein, conditional genetically engineered mouse models of estrogen receptor 1 (Esr1) and cytochrome P450 family 19 subfamily A member 1 (CYP19A1) were used to show that induction of Esr1 overexpression just before or with reproductive senescence and maintained through age 30 months resulted in significantly higher prevalence of estrogen receptor-positive adenocarcinomas than CYP19A1 overexpression. All adenocarcinomas tested showed high percentages of ER

Identifiants

pubmed: 36464513
pii: S0002-9440(22)00317-0
doi: 10.1016/j.ajpath.2022.09.008
pmc: PMC9768686
pii:
doi:

Substances chimiques

Estrogen Receptor alpha 0
Cyp19a1 protein, mouse EC 1.14.14.1
Esr1 protein, mouse 0
Aromatase EC 1.14.14.1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

103-120

Subventions

Organisme : NCI NIH HHS
ID : P30 CA051008
Pays : United States
Organisme : NCI NIH HHS
ID : UH2 CA213388
Pays : United States
Organisme : NCI NIH HHS
ID : UH3 CA213388
Pays : United States

Informations de copyright

Copyright © 2023 American Society for Investigative Pathology. Published by Elsevier Inc. All rights reserved.

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Auteurs

Priscilla A Furth (PA)

Department of Oncology, Georgetown University, Washington, District of Columbia; Department of Medicine, Georgetown University, Washington, District of Columbia. Electronic address: paf3@georgetown.edu.

Weisheng Wang (W)

Department of Oncology, Georgetown University, Washington, District of Columbia.

Keunsoo Kang (K)

Department of Microbiology, College of Science and Technology, Dankook University, Cheonan, Republic of Korea.

Brendan L Rooney (BL)

Department of Oncology, Georgetown University, Washington, District of Columbia.

Grace Keegan (G)

Department of Oncology, Georgetown University, Washington, District of Columbia.

Vinona Muralidaran (V)

Department of Oncology, Georgetown University, Washington, District of Columbia.

Justin Wong (J)

Department of Oncology, Georgetown University, Washington, District of Columbia.

Charles Shearer (C)

Department of Oncology, Georgetown University, Washington, District of Columbia.

Xiaojun Zou (X)

Department of Oncology, Georgetown University, Washington, District of Columbia.

Jodi A Flaws (JA)

Department of Comparative Biosciences, University of Illinois Urbana-Champaign, Urbana, Illinois.

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Classifications MeSH