Skeletal muscle atrophy and dysfunction in breast cancer patients: role for chemotherapy-derived oxidant stress

Abstract

How breast cancer and its treatments affect skeletal muscle is not well defined. To address this question, we assessed skeletal muscle structure and protein expression in 13 women who were diagnosed with breast cancer and receiving adjuvant chemotherapy following tumor resection and 12 nondiseased controls. Breast cancer patients showed reduced single-muscle fiber cross-sectional area and fractional content of subsarcolemmal and intermyofibrillar mitochondria. Drugs commonly used in breast cancer patients (doxorubicin and paclitaxel) caused reductions in myosin expression, mitochondrial loss, and increased reactive oxygen species (ROS) production in C2C12 murine myotube cell cultures, supporting a role for chemotherapeutics in the atrophic and mitochondrial phenotypes. Additionally, concurrent treatment of myotubes with the mitochondrial-targeted antioxidant MitoQ prevented chemotherapy-induced myosin depletion, mitochondrial loss, and ROS production. In patients, reduced mitochondrial content and size and increased expression and oxidation of peroxiredoxin 3, a mitochondrial peroxidase, were associated with reduced muscle fiber cross-sectional area. Our results suggest that chemotherapeutics may adversely affect skeletal muscle in patients and that these effects may be driven through effects of these drugs on mitochondrial content and/or ROS production.

Document Details

Document Type
Pub Defense Publication
Publication Date
Nov 01, 2018
Source ID
10.1152/ajpcell.00002.2018

Entities

People

  • Bethany Korwin-mihavics
  • Blas A Guigni
  • Brad Fiske
  • Damien M. Callahan
  • Kim Dittus
  • Mark S. Miller
  • Michael J. Toth
  • Thomas Voigt
  • Timothy W. Tourville
  • Vikas Anathy

Organizations

  • National Cancer Institute
  • National Institute of Arthritis and Musculoskeletal and Skin Diseases
  • National Institute of General Medical Sciences
  • United States Department of Defense
  • University of Massachusetts Amherst
  • University of Vermont

Tags

Fields of Study

  • Biology
  • Medicine

Readers

  • Immunology and Pathology
  • Molecular and Cellular Biology
  • Oncology (Cancer Research).