Evidence map›Paper›PMID 34410380›Full record

ArticleEndocrinology2021

Breast Cancer Endocrine Therapy Promotes Weight Gain With Distinct Adipose Tissue Effects in Lean and Obese Female Mice.

Rebecca L Scalzo, Rebecca M Foright, Sara E Hull, Leslie A Knaub, Stevi Johnson-Murguia, Fotobari Kinanee, Jeffrey Kaplan, Julie A Houck, Ginger Johnson, Rachel R Sharp and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in Endocrinology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.4field-weighted citation impact, top 15% 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

24 citing papers in PubMed, 26 citations in OpenAlex.

  1. Trial
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  6. Weight change and diabetes risk following breast cancer: a nationwide cohort study.Journal of cancer survivorship : research and practice · 2025
    Article
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  18. The 'omics of obesity in B-cell acute lymphoblastic leukemia.Journal of the National Cancer Institute. Monographs · 2023
    Article
  19. Article
  20. Article
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

18 authors at 5 institutions in 3 countries.

Rebecca L ScalzoDivision of Endocrinology, Metabolism & Diabetes, Department of Medicine; University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Rebecca M ForightDepartment of Anatomy and Cell Biology, University of Kansas Medical Center, Kansas City, KS 66160, USA.
Sara E HullDivision of Endocrinology, Metabolism & Diabetes, Department of Medicine; University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Leslie A KnaubDivision of Endocrinology, Metabolism & Diabetes, Department of Medicine; University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Stevi Johnson-MurguiaDepartment of Pathology, University of Oklahoma Health Sciences Center, Stephenson Cancer Center, Harold Hamm Diabetes Research Center, Oklahoma City, OK 73104, USA.
Fotobari KinaneeDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Jeffrey KaplanDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Julie A HouckDivision of Endocrinology, Metabolism & Diabetes, Department of Medicine; University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Ginger JohnsonDivision of Endocrinology, Metabolism & Diabetes, Department of Medicine; University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Rachel R SharpDepartment of Cell Biology, University of Oklahoma Health Sciences Center, Stephenson Cancer Center, Harold Hamm Diabetes Research Center, Oklahoma City, OK 73104, USA.
Austin E GillenDivision of Hematology, Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Kenneth L JonesDepartment of Cell Biology, University of Oklahoma Health Sciences Center, Stephenson Cancer Center, Harold Hamm Diabetes Research Center, Oklahoma City, OK 73104, USA.
Anni M Y ZhangDiabetes Research Group, Life Sciences Institute, Department of Cellular and Physiological Sciences, Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada.
James D JohnsonDiabetes Research Group, Life Sciences Institute, Department of Cellular and Physiological Sciences, Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada.ORCID 0000-0002-7523-9433
Paul S MacLeanDivision of Endocrinology, Metabolism & Diabetes, Department of Medicine; University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Jane E B ReuschDivision of Endocrinology, Metabolism & Diabetes, Department of Medicine; University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Sabrina Wright-HobartDepartment of Pathology, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Elizabeth A WellbergCenter for Women's Health Research; University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.ORCID 0000-0001-7342-390X
Diabetes Australia · AUUniversity of Colorado Anschutz Medical Campus · USUniversity of Oklahoma Health Sciences Center · USUniversity of British Columbia · CAUniversity of Kansas Medical Center · US

Funding

University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
PILOT STUDY--SUBSTRATE METABOLISM IN EXTREMELY LOW BIRTH WEIGHT INFANTSP30DK048520 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI JANINE A HIGGINS · 1995 to 2026
$32.6M
Colorado Clinical and Translational Science Institute (UL1)UL1TR000154 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2012 to 2013
$20.4M
Suppression of ERalpha in Hematopoietic Stem Cell-Derived Adipocytes Increases Adiposity via Kynurenine and the Aryl Hydrocarbon ReceptorU54AG062319 · NIA · UNIVERSITY OF COLORADO DENVER · PI JUDITH G. REGENSTEINER · 2018 to 2026
$13.5M
Institutional Career Development CoreKL2TR002534 · NCATS · UNIVERSITY OF COLORADO DENVER · PI BURNHAM, ELLEN L · 2018 to 2022
$4.6M
Transdisciplinary Research in Energetics and Cancer (TREC) Training GrantR25CA203650 · NCI · YALE UNIVERSITY · PI IRWIN, MELINDA L · 2016 to 2025
$2.9M
Growth Factor Signaling in Obesity Associated Breast CancerR01CA241156 · NCI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI WELLBERG, ELIZABETH · 2019 to 2023
$1.6M
A Narrowed Window for Targeting Metabolic Flexibility in Breast Cancer PreventionR01CA164166 · NCI · UNIVERSITY OF COLORADO DENVER · PI MACLEAN, PAUL S., SCHEDIN, PEPPER J · 2013 to 2017
$1.6M
Cardiovascular Mechanisms of Exercise Intolerance in Diabetes and the Role of SexI01CX001532 · VA · VA EASTERN COLORADO HEALTH CARE SYSTEM · PI REUSCH, JANE E · 2017 to 2022
–
The Interaction of Diabetes and Estrogen on Skeletal Muscle BioenergeticsIK2BX004533 · VA · VA EASTERN COLORADO HEALTH CARE SYSTEM · PI SCALZO, REBECCA L · 2019 to 2024
–
Targeting Microvascular Contributors to Impaired Functional Exercise Capacity in DiabetesI01BX002046 · VA · VA EASTERN COLORADO HEALTH CARE SYSTEM · PI REUSCH, JANE E · 2014 to 2024
–
BLRD VA I01 BX002046BLRD VA IK2 BX004533CSRD VA I01 CX001532NCATS NIH HHS KL2 TR002534NCATS NIH HHS UL1 TR000154NCI NIH HHS P30 CA046934NCI NIH HHS R01 CA164166NCI NIH HHS R01 CA241156NCI NIH HHS R25 CA203650NIA NIH HHS U54 AG062319NIDDK NIH HHS P30 DK048520
6 · The paper itself

Abstract

Breast cancer survivors treated with tamoxifen and aromatase inhibitors report weight gain and have an elevated risk of type 2 diabetes, especially if they have obesity. These patient experiences are inconsistent with, preclinical studies using high doses of tamoxifen which reported acute weight loss. We investigated the impact of breast cancer endocrine therapies in a preclinical model of obesity and in a small group of breast adipose tissue samples from women taking tamoxifen to understand the clinical findings. Mature female mice were housed at thermoneutrality and fed either a low-fat/low-sucrose (LFLS) or a high-fat/high-sucrose (HFHS) diet. Consistent with the high expression of Esr1 observed in mesenchymal stem cells from adipose tissue, endocrine therapy was associated with adipose accumulation and more preadipocytes compared with estrogen-treated control mice but resulted in fewer adipocyte progenitors only in the context of HFHS. Analysis of subcutaneous adipose stromal cells revealed diet- and treatment-dependent effects of endocrine therapies on various cell types and genes, illustrating the complexity of adipose tissue estrogen receptor signaling. Breast cancer therapies supported adipocyte hypertrophy and associated with hepatic steatosis, hyperinsulinemia, and glucose intolerance, particularly in obese females. Current tamoxifen use associated with larger breast adipocyte diameter only in women with obesity. Our translational studies suggest that endocrine therapies may disrupt adipocyte progenitors and support adipocyte hypertrophy, potentially leading to ectopic lipid deposition that may be linked to a greater type 2 diabetes risk. Monitoring glucose tolerance and potential interventions that target insulin action should be considered for some women receiving life-saving endocrine therapies for breast cancer.

Indexed as

ObesityAdipose TissueAnimalsAntineoplastic Agents, HormonalAromatase InhibitorsFemaleHumansMammary Neoplasms, ExperimentalMiceMice, Inbred C57BLMice, ObeseTamoxifenThinnessWeight GainAntineoplastic Agents, HormonalAromatase InhibitorsTamoxifenadipocyte progenitorendocrine therapyObesitytamoxifenthermoneutralityweight gain

Identifiers

PMID34410380
PMCPMC8455348
OpenAlexW3194167116

What OpenQuestion holds

Textmetadata
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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.