Evidence map›Paper›PMID 38611051›Full record

ArticleCancers2024

Long-Term Oral Tamoxifen Administration Decreases Brain-Derived Neurotrophic Factor in the Hippocampus of Female Long-Evans Rats.

Laura E Been, Amanda R Halliday, Sarah M Blossom, Elena M Bien, Anya G Bernhard, Grayson E Roth, Karina I Domenech Rosario, Karlie B Pollock, Petra E Abramenko, Leily M Behbehani and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.7field-weighted citation impact, top 16% of its field
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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. A sexually dimorphic neuronal cluster in the mouse medial amygdala responds to male sexual status.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. 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

12 authors at 1 institution in 1 country.

Laura E BeenDepartment of Psychology and Neuroscience Program, Haverford College, Haverford, PA 19041, USA.ORCID 0000-0002-6493-5265
Amanda R HallidayDepartment of Psychology and Neuroscience Program, Haverford College, Haverford, PA 19041, USA.
Sarah M BlossomDepartment of Psychology and Neuroscience Program, Haverford College, Haverford, PA 19041, USA.
Elena M BienDepartment of Psychology and Neuroscience Program, Haverford College, Haverford, PA 19041, USA.
Anya G BernhardDepartment of Psychology and Neuroscience Program, Haverford College, Haverford, PA 19041, USA.
Grayson E RothDepartment of Psychology and Neuroscience Program, Haverford College, Haverford, PA 19041, USA.
Karina I Domenech RosarioDepartment of Psychology and Neuroscience Program, Haverford College, Haverford, PA 19041, USA.
Karlie B PollockDepartment of Psychology and Neuroscience Program, Haverford College, Haverford, PA 19041, USA.
Petra E AbramenkoDepartment of Psychology and Neuroscience Program, Haverford College, Haverford, PA 19041, USA.ORCID 0009-0007-0646-9706
Leily M BehbehaniDepartment of Psychology and Neuroscience Program, Haverford College, Haverford, PA 19041, USA.
Gabriel J PascalDepartment of Psychology and Neuroscience Program, Haverford College, Haverford, PA 19041, USA.ORCID 0009-0003-3713-4870
Mary Ellen KellyDepartment of Psychology and Neuroscience Program, Haverford College, Haverford, PA 19041, USA.ORCID 0000-0002-6564-9455
Haverford College · US

Funding

Haverford College Department of Psychology
6 · The paper itself

Abstract

Tamoxifen, a selective estrogen receptor modulator (SERM), is commonly used as an adjuvant drug therapy for estrogen-receptor-positive breast cancers. Though effective at reducing the rate of cancer recurrence, patients often report unwanted cognitive and affective side effects. Despite this, the impacts of chronic tamoxifen exposure on the brain are poorly understood, and rodent models of tamoxifen exposure do not replicate the chronic oral administration seen in patients. We, therefore, used long-term ad lib consumption of medicated food pellets to model chronic tamoxifen exposure in a clinically relevant way. Adult female Long-Evans Hooded rats consumed tamoxifen-medicated food pellets for approximately 12 weeks, while control animals received standard chow. At the conclusion of the experiment, blood and brain samples were collected for analyses. Blood tamoxifen levels were measured using a novel ultra-performance liquid chromatography-tandem mass spectrometry assay, which found that this administration paradigm produced serum levels of tamoxifen similar to those in human patients. In the brain, brain-derived neurotrophic factor (BDNF) was visualized in the hippocampus using immunohistochemistry. Chronic oral tamoxifen treatment resulted in a decrease in BDNF expression across several regions of the hippocampus. These findings provide a novel method of modeling and measuring chronic oral tamoxifen exposure and suggest a putative mechanism by which tamoxifen may cause cognitive and behavioral changes reported by patients.

Indexed as

animal modelbrainbreast cancercognitionestrogen receptorgrowth factorhormone therapymemory

Identifiers

PMID38611051
PMCPMC11010888
OpenAlexW4393353288

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.