Evidence of sex differences in cancer-related cardiac complications in mouse models of pancreatic and liver cancer.


Journal

Physiological reports
ISSN: 2051-817X
Titre abrégé: Physiol Rep
Pays: United States
ID NLM: 101607800

Informations de publication

Date de publication:
04 2023
Historique:
revised: 16 03 2023
received: 23 09 2022
accepted: 29 03 2023
medline: 28 4 2023
pubmed: 27 4 2023
entrez: 27 4 2023
Statut: ppublish

Résumé

Abnormal heart rate variability (HRV) is commonly observed in cancer patients who have undergone targeted therapy and/or surgery, yet the effects of cancer itself on cardiac function remain underexplored. Specifically, there is limited knowledge about sex-specific manifestations of HRV in cancer patients. Transgenic mouse models are widely used to study different types of cancer. Here, we aimed to investigate the sex-specific effects of cancer on cardiac function using transgenic mouse models of pancreatic and liver cancers. This study used male and female transgenic mice with cancer and wild-type controls. Cardiac function was assessed by recording electrocardiograms in conscious mice. RR intervals were detected to determine HRV using time and frequency domain analyses. Histological analysis with Masson's trichrome staining was performed to determine structural changes. In females, increased HRV was observed in both pancreatic and liver cancer-bearing mice. In contrast, in males, increased HRV was observed only in the liver cancer group. Male pancreatic cancer mice demonstrated autonomic balance shift showing an increase in parasympathetic to sympathetic tone. The heart rate (HR) was higher in control and liver cancer male mice groups than in females. Histological analysis did not show significant sex differences but suggested a higher degree of remodeling in liver cancer mice than in control, specifically in the right atrium and left ventricle. This study revealed sex differences in cancer's HR modulation. Specifically, female cancer mice had lower median HR and higher HRV. These findings indicate that sex must be considered when using HRV as a cancer biomarker.

Identifiants

pubmed: 37102225
doi: 10.14814/phy2.15672
pmc: PMC10133859
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e15672

Informations de copyright

© 2023 The Authors. Physiological Reports published by Wiley Periodicals LLC on behalf of The Physiological Society and the American Physiological Society.

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Auteurs

Anna Gams (A)

Department of Biomedical Engineering, The George Washington University, Washington, District of Columbia, USA.

Alejandro Nevarez (A)

Department of Biomedical Engineering, The George Washington University, Washington, District of Columbia, USA.

Stephanie Perkail (S)

The George Washington Cancer Center, The George Washington University School of Medicine and Health Sciences, Washington, District of Columbia, USA.

Aileen Venegas (A)

Department of Biomedical Engineering, The George Washington University, Washington, District of Columbia, USA.

Sharon A George (SA)

Department of Biomedical Engineering, The George Washington University, Washington, District of Columbia, USA.
Department of Biomedical Engineering, Northwestern University, Chicago, Illinois, USA.

Tatiana Efimova (T)

The George Washington Cancer Center, The George Washington University School of Medicine and Health Sciences, Washington, District of Columbia, USA.
Department of Anatomy and Cell Biology, The George Washington University School of Medicine and Health Sciences, Washington, District of Columbia, USA.

Igor R Efimov (IR)

Department of Biomedical Engineering, The George Washington University, Washington, District of Columbia, USA.
Department of Biomedical Engineering, Northwestern University, Chicago, Illinois, USA.
Department of Medicine, Northwestern University, Chicago, Illinois, USA.

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Classifications MeSH