Pre- and Postoperative Antioxidant Use, Aryl Hydrocarbon Receptor (AhR) Activation and Clinical Outcome in Different Treatment Groups of Breast Cancer Patients.

Breast cancer Chemotherapy Cohort Endocrine treatment Radiation therapy

Journal

Clinical breast cancer
ISSN: 1938-0666
Titre abrégé: Clin Breast Cancer
Pays: United States
ID NLM: 100898731

Informations de publication

Date de publication:
21 Dec 2023
Historique:
received: 18 09 2023
revised: 08 12 2023
accepted: 10 12 2023
medline: 3 2 2024
pubmed: 3 2 2024
entrez: 2 2 2024
Statut: aheadofprint

Résumé

Cancer patients often use antioxidants that may interact with adjuvant treatments. The purpose was to investigate pre- and postoperative antioxidant use in relation to clinicopathological characteristics and prognosis in different breast cancer treatment groups. Pre- and postoperative antioxidant (vitamin A, C, E, carotenoids, or Q10) or multivitamin use was self-reported by patients from Lund (n = 1855) and Helsingborg (n=478), Sweden. Patients were followed for up to 15 years. Clinical data were obtained from patient charts. The aryl hydrocarbon receptor (AhR) was evaluated in tumor tissue arrays from 915 patients from Lund and with Western blot in MCF-7 and MDA-MB-231 cells. About 10% of patients used antioxidants. Nuclear AhR (AhR The clinical impact of antioxidants depended on antioxidant type, timing of use, and tumor AhR activation. Antioxidants may influence clinical outcome by activation of the master regulator AhR in addition to interference with free radicals. Further studies are needed to identify breast patients that might improve or worsen their prognosis when using antioxidants postoperatively.

Sections du résumé

BACKGROUND BACKGROUND
Cancer patients often use antioxidants that may interact with adjuvant treatments. The purpose was to investigate pre- and postoperative antioxidant use in relation to clinicopathological characteristics and prognosis in different breast cancer treatment groups.
METHODS AND PATIENTS METHODS
Pre- and postoperative antioxidant (vitamin A, C, E, carotenoids, or Q10) or multivitamin use was self-reported by patients from Lund (n = 1855) and Helsingborg (n=478), Sweden. Patients were followed for up to 15 years. Clinical data were obtained from patient charts. The aryl hydrocarbon receptor (AhR) was evaluated in tumor tissue arrays from 915 patients from Lund and with Western blot in MCF-7 and MDA-MB-231 cells.
RESULTS RESULTS
About 10% of patients used antioxidants. Nuclear AhR (AhR
CONCLUSION CONCLUSIONS
The clinical impact of antioxidants depended on antioxidant type, timing of use, and tumor AhR activation. Antioxidants may influence clinical outcome by activation of the master regulator AhR in addition to interference with free radicals. Further studies are needed to identify breast patients that might improve or worsen their prognosis when using antioxidants postoperatively.

Identifiants

pubmed: 38307727
pii: S1526-8209(23)00306-3
doi: 10.1016/j.clbc.2023.12.002
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2023 The Author(s). Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Disclosure KI has received speaker honorarium from Pierre Fabre. The other authors declare no conflicts of interest.

Auteurs

Linn Nilsson (L)

Department of Clinical Sciences Lund, Division of Oncology, Lund University, Lund, Sweden; Department of Medical Physics and Engineering, Växjö Central Hospital and Department of Research and Development, Region Kronoberg, Växjö, Sweden.

Somayeh Khazaei (S)

Department of Clinical Sciences Lund, Division of Oncology, Lund University, Lund, Sweden.

Helga Tryggvadottir (H)

Department of Clinical Sciences Lund, Division of Oncology, Lund University, Lund, Sweden; Department of Hematology, Oncology, and Radiation Physics, Skåne University Hospital, Lund, Sweden.

Sofie Björner (S)

Department of Clinical Sciences Lund, Division of Oncology, Lund University, Lund, Sweden.

Alessandra Bressan (A)

Department of Clinical Sciences Lund, Division of Oncology, Lund University, Lund, Sweden.

Karin Jirström (K)

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

Gabriel Adrian (G)

Department of Clinical Sciences Lund, Division of Oncology, Lund University, Lund, Sweden; Department of Hematology, Oncology, and Radiation Physics, Skåne University Hospital, Lund, Sweden.

Anna-Karin Falck (AK)

Department of Surgery, Helsingborg Hospital, Helsingborg, Sweden.

Signe Borgquist (S)

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

Karolin Isaksson (K)

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

Helena Jernström (H)

Department of Clinical Sciences Lund, Division of Oncology, Lund University, Lund, Sweden. Electronic address: helena.jernstrom@med.lu.se.

Classifications MeSH