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Copyright ©The Author(s) 2026. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Clin Oncol. Jan 24, 2026; 17(1): 112039
Published online Jan 24, 2026. doi: 10.5306/wjco.v17.i1.112039
Acute exercise-induced catecholaminergic responses after 16 weeks of community-based exercise training in early-stage breast cancer survivors
Jeb F Struder, Aiden J Chauntry, Lauren C Bates-Fraser, Elizabeth P Harrell, Jordan T Lee, Chad W Wagoner, Stephanie A Sullivan, David B Bartlett, Hyman B Muss, Brian C Jensen, Claudio L Battaglini, Erik D Hanson
Jeb F Struder, Aiden J Chauntry, Lauren C Bates-Fraser, Elizabeth P Harrell, Jordan T Lee, Chad W Wagoner, Stephanie A Sullivan, Claudio L Battaglini, Erik D Hanson, Department of Exercise and Sport Science, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, United States
Lauren C Bates-Fraser, Jordan T Lee, Chad W Wagoner, Claudio L Battaglini, Erik D Hanson, Human Movement Science Curriculum, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, United States
Lauren C Bates-Fraser, Jordan T Lee, Hyman B Muss, Claudio L Battaglini, Erik D Hanson, Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, United States
Chad W Wagoner, Department of Kinesiology, Recreation, and Sport Studies, University of Tennessee, Knoxville, TN 37996, United States
David B Bartlett, School of Biosciences, University of Surrey, Guildford GU2 7XH, Surrey, United Kingdom
David B Bartlett, Division of Medical Oncology, Duke Cancer Institute, Duke University, Durham, NC 27710, United States
Hyman B Muss, Department of Hematology Oncology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, United States
Brian C Jensen, Department of Medicine, Division of Cardiology, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, United States
Author contributions: Battaglini CL, Hanson ED, and Muss HB acquired necessary funding support for the study; Bartlett DB, Battaglini CL, and Hanson ED supervised project administration, developed study methodology, and contributed to conceptualization in correspondence with Wagoner CW and Lee JT; Bates-Fraser LC, Hanson ED, Harrell EP, Jensen BC, Lee JT, Struder JF, Sullivan SA, and Wagoner CW conducted the investigation; Chauntry AJ and Struder JF performed the statistical analysis with visualizations provided by Struder JF; Hanson ED and Struder JF drafted and revised the manuscript, with final manuscript approval received from all co-authors.
Supported by the Breast Cancer Research Foundation of New York, NY, No. BCRF-17-112; the National Cancer Institute’s National Research Service Award sponsored by the Lineberger Comprehensive Cancer Center at the University of North Carolina, No. T32 CA116339; and the National Heart, Lung, and Blood Institute of the National Institutes of Health, No. R01HL162805 and No. R01HL157187.
Institutional review board statement: The study was approved by the Protocol Review Committee at the Lineberger Comprehensive Cancer Center (LCCC1630: Get REAL and HEEL Research Program) and by the Institutional Review Board of UNC-Chapel Hill (IRB #16-3284).
Clinical trial registration statement: This study is registered at ClinicalTrials.gov with the Get REAL and HEEL Research Program. The registration identification number is NCT03760536.
Informed consent statement: All study participants provided informed written consent prior to study enrollment.
Conflict-of-interest statement: All authors report having no relevant conflicts of interest for this article.
CONSORT 2010 statement: The design of this project was a non-randomized control trial. As such, we do not believe that the CONSORT 2010 statement applies in this situation.
Data sharing statement: Data set available from the corresponding author (Erik Hanson; edhanson@email.unc.edu) upon reasonable request.
Open Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/
Corresponding author: Erik D Hanson, PhD, Associate Professor, Department of Exercise and Sport Science, University of North Carolina at Chapel Hill, Exercise Oncology Research Laboratory, Campus Box #8700, Chapel Hill, NC 27599, United States. edhanson@email.unc.edu
Received: July 16, 2025
Revised: August 19, 2025
Accepted: December 8, 2025
Published online: January 24, 2026
Processing time: 188 Days and 17.3 Hours
Abstract
BACKGROUND

Breast cancer survivors (BCS) demonstrate attenuated immune cell mobilization following acute exercise, with partial restoration following exercise training. Epinephrine (EPI) and norepinephrine (NE) are responsive to exercise-stress and directly regulate immune cell function, indicating a potential role in this restorative process. Similar attenuations in catecholaminergic signaling have been reported in BCS post-exercise; however, it is unknown whether this is maintained within a trained state. We hypothesized that compared to non-cancer controls (CON), acute exercise would induce an attenuated catecholaminergic response in untrained BCS, which would be recovered to levels similar to CON after training.

AIM

To compare acute exercise-induced catecholaminergic responses between BCS and CON before (PRE) and after (POST) completing a community-based exercise intervention.

METHODS

Thirteen BCS (age: 56 ± 2 years, body fat: 39.7% ± 1.3%) and 13 CON (age: 56 ± 2 years, body fat: 41.2% ± 1.7%) performed 45 minutes of intermittent cycling at 60% peak power output PRE and POST 16 weeks of community-based exercise training. Blood samples were collected at baseline (BASE), immediately (0 hour), and 1-hour (1 hour) post-exercise for assessment of the acute EPI and NE response. Separate linear mixed models were used for PRE and POST EPI and NE assessment.

RESULTS

At PRE, both BCS and CON demonstrated increases in EPI (+87.4 pg∙mL-1, P < 0.001) and NE (+1295 pg∙mL-1, P < 0.001) at 0 hour, with no group differences. At POST, group differences in NE initiation (0 hour-BASE) were not statistically significant (-544.9 pg∙mL-1, P = 0.115, g = 0.92), despite divergent responses between BCS (+28%, P = 0.175, g = 0.36) and CON (-13%, P = 0.377, g = 0.23). No group differences were observed for NE recovery (1 hour-0 hour) nor for EPI initiation or recovery.

CONCLUSION

BCS and CON present with similar exercise-induced catecholaminergic responses regardless of training, suggesting an alternative mechanism may have made a greater contribution to the training-induced immune cell revival previously observed.

Keywords: Autonomic function; Breast neoplasms; Cancer survivorship; Cardiovascular stress response; Catecholamines; Exercise therapy; Sympathetic nervous system

Core Tip: Exercise training partially restored immune cell responses previously diminished within untrained breast cancer survivors (BCS) immediately post-exercise. Epinephrine and norepinephrine are exercise-responsive and regulate immune cell function, suggesting a role in this training-induced restoration. Acute exercise induces similar BCS catecholaminergic attenuation; however, it is unclear whether this is sustained post-training. In this study, we aimed to compare acute exercise-induced catecholaminergic responses between BCS and non-cancer controls (CON) before and after a training intervention. BCS and CON presented with similar exercise-induced catecholaminergic responses regardless of training, suggesting the immune cell revival previously observed may be regulated by alternative mechanisms.