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2026-06-27 PubMed

Strength Training During Chemotherapy Elevates IL-6, IL-17 in Breast Cancer, No Autophagy Changes

The Effect of Strength Training During Chemotherapy in Women With Breast Cancer on Serum Cytokine Concentrations and Skeletal Muscle Autophagy-Related Proteins.

Background

Chemotherapy for breast cancer often leads to debilitating side effects like fatigue, muscle weakness, and inflammation, contributing to treatment non-completion and reduced quality of life. These toxicities are partly mediated by systemic inflammation and altered muscle metabolism, including processes like autophagy, which are crucial for cellular maintenance and adaptation to stress. Understanding how interventions like exercise impact these pathways could offer strategies to mitigate adverse effects. This study investigates if strength training can modulate inflammatory cytokines and muscle autophagy during chemotherapy, addressing a critical gap in supportive care.

Study Design

Researchers randomized women with breast cancer to either a strength training group (n = 23) or a usual care group (n = 17) during chemotherapy. The training group completed supervised strength training twice weekly throughout their chemotherapy regimen, while the usual care group maintained habitual physical activity. Assessments were conducted pre-chemotherapy (T0) and post-chemotherapy/intervention (T1). Primary endpoints included quantifying serum cytokines (IFN-γ, IL-1RA, IL-6, IL-8, IL-10, IL-17, MCP-1, TNF-α) and analyzing muscle biopsies for autophagy- and heat-shock-related proteins using unspecified biochemical assays. Exploratory analyses also assessed associations between changes in physiological outcomes (strength, fitness, capillary density) and biomarker responses.

Results

In the strength training group, mean serum IL-6 significantly increased from 1.21 ± 0.47 to 1.69 ± 0.71 pg/mL, and IL-17 rose from 1.24 ± 0.25 to 2.18 ± 0.87 pg/mL. While IFN-γ also increased in the training group (from 14.4 ± 8.6 to 28.8 ± 17.3 pg/mL), the group×time interaction for IFN-γ was not statistically significant. Conversely, IL-6 and IL-17 decreased in the usual care group over the same period. No significant changes were observed in other measured cytokines, nor in any of the targeted skeletal muscle autophagy- or heat-shock-related proteins across either group. Exploratory analyses revealed no associations between changes in muscle strength and autophagy proteins, cardiorespiratory fitness and cytokines, or capillary density and cytokines. This suggests a dissociation between the systemic inflammatory response and local muscle protein regulation in this context.

Despite significant group differences in IL-6 and IL-17 over time, strength training during chemotherapy did not alter selected skeletal muscle autophagy- or heat-shock-related proteins.

Key Findings

  • Strength training during chemotherapy increased serum IL-6 from 1.21 ± 0.47 to 1.69 ± 0.71 pg/mL in breast cancer patients.
  • Serum IL-17 also increased significantly in the strength training group, from 1.24 ± 0.25 to 2.18 ± 0.87 pg/mL.
  • IL-6 and IL-17 decreased in the usual care group during chemotherapy.
  • No changes were observed in skeletal muscle autophagy- or heat-shock-related proteins in either group.
  • No associations were found between changes in strength, fitness, or capillary density and cytokine or autophagy protein responses.

Why It Matters

This study provides initial evidence that strength training during chemotherapy can modulate systemic inflammation in breast cancer patients, specifically by increasing IL-6 and IL-17. While the clinical significance of these cytokine shifts remains uncertain, it highlights a potential immunological impact of exercise during treatment. For patients and clinicians, this suggests that supervised strength training, even if it doesn't directly alter muscle autophagy proteins in the short term, is not detrimental and may influence systemic inflammatory markers. Further research is needed to understand if these cytokine changes are beneficial, harmful, or merely transient, and how they might relate to long-term outcomes or specific chemotherapy regimens. The lack of change in muscle autophagy proteins indicates that the observed systemic inflammatory response might not directly translate to immediate, measurable changes in these specific muscle maintenance pathways, suggesting other mechanisms may be at play for muscle preservation.


breast cancer chemotherapy strength training cytokines inflammation muscle health
Source: pubmed:42350900 · Ingested 2026-06-27 · Digest: gemini-2.5-flash