The Prognostic Impact of Intratumoral Aryl Hydrocarbon Receptor in Primary Breast Cancer Depends on the Type of Endocrine Therapy: A Population-Based Cohort Study.

aryl hydrocarbon receptor breast cancer endocrine therapy intratumoral aromatase polymorphisms prognosis

Journal

Frontiers in oncology
ISSN: 2234-943X
Titre abrégé: Front Oncol
Pays: Switzerland
ID NLM: 101568867

Informations de publication

Date de publication:
2021
Historique:
received: 13 01 2021
accepted: 22 04 2021
entrez: 7 6 2021
pubmed: 8 6 2021
medline: 8 6 2021
Statut: epublish

Résumé

The aryl hydrocarbon receptor (AhR) is a master regulator of multiple pathways involved in breast cancer, and influences the estrogen receptor alpha (ER) and aromatase/CYP19A1. The purpose of this study was to elucidate the interplay between intratumoral levels of AhR and aromatase, patient characteristics (including

Identifiants

pubmed: 34094928
doi: 10.3389/fonc.2021.642768
pmc: PMC8174786
doi:

Types de publication

Journal Article

Langues

eng

Pagination

642768

Informations de copyright

Copyright © 2021 Tryggvadottir, Sandén, Björner, Bressan, Ygland Rödström, Khazaei, Edwards, Nodin, Jirström, Isaksson, Borgquist and Jernström.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Helga Tryggvadottir (H)

Division of Oncology, Department of Clinical Sciences, Lund, Lund University and Skåne University Hospital, Lund, Sweden.

Emma Sandén (E)

Division of Oncology, Department of Clinical Sciences, Lund, Lund University and Skåne University Hospital, Lund, Sweden.

Sofie Björner (S)

Division of Oncology, Department of Clinical Sciences, Lund, Lund University and Skåne University Hospital, Lund, Sweden.

Alessandra Bressan (A)

Division of Oncology, Department of Clinical Sciences, Lund, Lund University and Skåne University Hospital, Lund, Sweden.

Maria Ygland Rödström (M)

Division of Oncology, Department of Clinical Sciences, Lund, Lund University and Skåne University Hospital, Lund, Sweden.

Somayeh Khazaei (S)

Division of Oncology, Department of Clinical Sciences, Lund, Lund University and Skåne University Hospital, Lund, Sweden.

Dean P Edwards (DP)

Department of Molecular & Cellular Biology and Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX, United States.

Björn Nodin (B)

Division of Oncology and Therapeutic Pathology, Department of Clinical Sciences, Lund, Lund University and Skåne University Hospital, Lund, Sweden.

Karin Jirström (K)

Division of Oncology and Therapeutic Pathology, Department of Clinical Sciences, Lund, Lund University and Skåne University Hospital, Lund, Sweden.

Karolin Isaksson (K)

Division of Surgery, Department of Clinical Sciences, Lund, Lund University, Lund, Sweden.
Department of Surgery, Kristianstad Hospital, Kristianstad, Sweden.

Signe Borgquist (S)

Division of Oncology, Department of Clinical Sciences, Lund, Lund University and Skåne University Hospital, Lund, Sweden.
Department of Oncology, Aarhus University and Aarhus University Hospital, Aarhus, Denmark.

Helena Jernström (H)

Division of Oncology, Department of Clinical Sciences, Lund, Lund University and Skåne University Hospital, Lund, Sweden.

Classifications MeSH