Amino acid metabolism in cancer cachexia and chemotherapy myotoxicity

Am J Physiol Cell Physiol. 2025 Nov 1;329(5):C1451-C1467. doi: 10.1152/ajpcell.00085.2025. Epub 2025 Sep 10.

Abstract

Cancer-induced skeletal muscle wasting (cachexia) is responsible for over 20% of cancer-related deaths, yet much about the pathophysiology of the condition remains unknown. Importantly, cancer cachexia does not seem wholly responsive to traditional anabolic stimuli such as nutritional interventions. It is possible that tumors directly or indirectly target skeletal muscle for their dynamic and abundant pool of amino acids that can be reliably used by tumors to supplement energy production and biomass synthesis. Therefore, understanding how the presence of a tumor alters circulating and tissue-level amino acid pools could provide valuable insight into tumor-induced muscle wasting. The purpose of this review was to examine the current body of research that has studied amino acids in the context of cancer cachexia to better understand how amino acids behave during the development of cancer, cachexia, and various cancer chemotherapies. Distinct heterogeneity was observed in the behavior of amino acids when comparing weight-stable versus patients with cachectic cancer, and there may be important temporal considerations based on rhythmic changes in amino acid turnover and mealtimes. Overall, there was very little consistency in the reported fluctuations of amino acids from study to study, suggesting that there may be heterogeneous pathophysiology based on tumor type, stage, patient age, and comorbidities. Further work is required to characterize longitudinal changes in amino acid metabolism with consideration for these factors. Enhancing our understanding of amino acid metabolism during cancer cachexia could provide opportunities for advancement in practical methodologies in cachexia research and treatment strategies.

Keywords: amino acid; cachexia; cancer; muscle wasting; skeletal muscle.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acids* / metabolism
  • Animals
  • Antineoplastic Agents* / adverse effects
  • Cachexia* / chemically induced
  • Cachexia* / metabolism
  • Cachexia* / pathology
  • Energy Metabolism / drug effects
  • Humans
  • Muscle, Skeletal* / drug effects
  • Muscle, Skeletal* / metabolism
  • Muscle, Skeletal* / pathology
  • Muscular Atrophy* / chemically induced
  • Muscular Atrophy* / metabolism
  • Muscular Atrophy* / pathology
  • Neoplasms* / complications
  • Neoplasms* / drug therapy
  • Neoplasms* / metabolism
  • Neoplasms* / pathology

Substances

  • Amino Acids
  • Antineoplastic Agents