4.6 Article

A Time-Course Comparison of Skeletal Muscle Metabolomic Alterations in Walker-256 Tumour-Bearing Rats at Different Stages of Life

期刊

METABOLITES
卷 11, 期 6, 页码 -

出版社

MDPI
DOI: 10.3390/metabo11060404

关键词

cachexia; metabolomics; skeletal muscle; time-course; Walker-256 tumour

资金

  1. CAPES
  2. CNPq [302524/2016-9, 301771/20197]
  3. FAPESP [2015/21890-0, 2017/02739-4, 2018/20637-7, 2019/13937-7, 2019/14803-4, 2019/20558-2]

向作者/读者索取更多资源

Cancer cachexia is a severe wasting condition that requires further study to minimize damage and poor prognosis. Metabolic changes in skeletal muscle, especially increased amino acid levels and altered energetic metabolism, suggest an expressive catabolic process and diverted energy production, particularly in advanced tumor stages. Furthermore, the impact of cancer cachexia varies with host age, with more severe changes observed in weanling hosts throughout tumor evolution.
Cancer cachexia is a severe wasting condition that needs further study to find ways to minimise the effects of damage and poor prognosis. Skeletal muscle is the most impacted tissue in cancer cachexia; thus, elucidation of its metabolic alterations could provide a direct clue for biomarker research and be applied to detect this syndrome earlier. In addition, concerning the significant changes in the host metabolism across life, this study aimed to compare the metabolic muscle changes in cachectic tumour-bearing hosts at different ages. We performed H-1-NMR metabolomics in the gastrocnemius muscle in weanling and young adult Walker-256 tumour-bearing rats at different stages of tumour evolution (initial, intermediate, and advanced). Among the 49 metabolites identified, 24 were significantly affected throughout tumour evolution and 21 were significantly affected regarding animal age. The altered metabolites were mainly related to increased amino acid levels and changed energetic metabolism in the skeletal muscle, suggesting an expressive catabolic process and diverted energy production, especially in advanced tumour stages in both groups. Moreover, these changes were more severe in weanling hosts throughout tumour evolution, suggesting the distinct impact of cancer cachexia regarding the host's age, highlighting the need to adopting the right animal age when studying cancer cachexia.

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