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Preclinical study demonstrates that Litsea japonica fruit extract reduces muscle atrophy in cancer cachexia models, suggesting potential as a therapeutic supplement.
Cancer cachexia is a complex syndrome involved in muscle wasting, fat depletion, fatigue, reduced appetite, and unintentional weight loss. Recent studies have suggested that natural products can prevent cancer cachexia; however, there have been no studies on the effects of Litsea japonica fruit extract on cancer cachexia. This study aimed to identify compounds of L. japonica fruit extracted from water (LJFE‐W) and those extracted from 30% ethanol (LJFE‐E) for cancer cachexia treatment. In vitro and in vivo models were used for C26 conditioned medium (CM)‐induced C2C12 myotubes and C26 tumor‐bearing mice. We demonstrated that LJFE‐W and LJFE‐E regulated myostatin (MSTN), E3 ligase muscle‐specific RING finger protein‐1 (MuRF1), and muscular atrophy fbox‐1 protein (MAFbx32) expression in a CM‐induced in vitro model. LJFE‐E ameliorated conditioned medium‐induced myotube atrophy in cultured C2C12 myotubes. In contrast, LJFE‐W and LJFE‐E stimulated the Akt–mTOR signaling pathway for protein synthesis in C2C12 myotubes. In animal models, the LJFE‐E‐injected C26 tumor‐bearing group showed lower transcript‐level expression of MSTN, MuRF1, and MAFbx32 in the gastrocnemius muscles than the C26 tumor‐bearing group. LJFE ameliorated muscle atrophy in the cancer cachexia model by inhibiting MSTN. Thus, LJFE can be used as a supplement to cancer cachexia therapy.
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Woo et al. (2025) studied this question.
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