Evidence map›Paper›PMID 40646277›Full record

ArticleBJC reports2025

Interplay between AHR genotypes, lifestyle factors and adjuvant breast cancer treatments significantly impacts clinical outcome in a population-based cohort.

Annelie Augustinsson, Christopher Godina, Linn Nilsson, Kelin Gonçalves de Oliveira, Karolin Isaksson, Helena Jernström

Abstract read
In one paragraph

Article in BJC reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Annelie AugustinssonDepartment of Clinical Sciences in Lund, Oncology, Lund University and Lund University and Lund University Cancer Center LUCC/Kamprad, Lund, Sweden.ORCID http://orcid.org/0000-0003-3415-0536
Christopher GodinaDepartment of Clinical Sciences in Lund, Oncology, Lund University and Lund University and Lund University Cancer Center LUCC/Kamprad, Lund, Sweden.ORCID http://orcid.org/0000-0003-1501-0458
Linn NilssonDepartment of Clinical Sciences in Lund, Oncology, Lund University and Lund University and Lund University Cancer Center LUCC/Kamprad, Lund, Sweden.
Kelin Gonçalves de OliveiraDepartment of Clinical Sciences in Lund, Oncology, Lund University and Lund University and Lund University Cancer Center LUCC/Kamprad, Lund, Sweden.ORCID http://orcid.org/0000-0003-1646-5657
Karolin IsakssonDepartment of Clinical Sciences in Lund, Surgery, Lund University and Lund University Cancer Center LUCC, Lund, Sweden.ORCID http://orcid.org/0000-0003-3690-5680
Helena JernströmDepartment of Clinical Sciences in Lund, Oncology, Lund University and Lund University and Lund University Cancer Center LUCC/Kamprad, Lund, Sweden. helena.jernstrom@med.lu.se.ORCID http://orcid.org/0000-0002-2301-5147

Funding

Region Skåne Yngre ALFRegion Skåne, Sweden ALF 40620
6 · The paper itself

Abstract

backgroundThe purpose was to evaluate the prognostic impact of aryl hydrocarbon receptor (AHR) genotypes in relation to lifestyle and adjuvant treatments in breast cancer.

methodsAHR genotyping was performed on genomic DNA from 1701 patients included 2002-2016 in Lund, Sweden, and followed for up to 15 years. Eight AHR polymorphisms and eight haplotypes were analysed using survival and interaction analyses in relation to prognosis.

resultsHomozygosity for major allele frequencies was 42.1%-88.5%. AHR genotypes linked to lower AHR expression conferred differential prognosis combined with smoking, alcohol, antioxidant supplements, chemotherapy or endocrine therapy, with interactions between exposures and genotypes. Preoperative antioxidants combined with minor alleles of AHR_6 or AHR_9 conferred three-fold risks for breast cancer events, not seen in other patients (P

conclusionsThe prognostic impact of AHR genotypes depended on lifestyle and treatments, possibly due to the role of AhR as master regulator of metabolism, hypoxia, DNA repair and immune response. If confirmed, these findings may contribute to more personalised lifestyle recommendations and treatment.

Identifiers

PMID40646277
PMCPMC12254277

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.