Acknowledgement
This work was supported by the National Research Foundation of Korea (NRF) funded by the Korea government (MSIT) (NRF-2020R1C1C1007553, 2023R1A2C1005313 to Sung-Eun Kim, NRF-2022R1F1A1074668 to Min Jung Kim).
References
- Wang Y, Pessin JE. Mechanisms for fiber-type specificity of skeletal muscle atrophy. Curr Opin Clin Nutr Metab Care 2013; 16(3): 243-250. https://doi.org/10.1097/MCO.0b013e328360272d
- Schmidt M, Schuler SC, Huttner SS, von Eyss B, von Maltzahn J. Adult stem cells at work: regenerating skeletal muscle. Cell Mol Life Sci 2019; 76(13): 2559-2570. https://doi.org/10.1007/s00018-019-03093-6
- Bodine SC, Latres E, Baumhueter S, Lai VK, Nunez L, Clarke BA, et al. Identification of ubiquitin ligases required for skeletal muscle atrophy. Science 2001; 294(5547): 1704-1708. https://doi.org/10.1126/science.1065874
- Files DC, D'Alessio FR, Johnston LF, Kesari P, Aggarwal NR, Garibaldi BT, et al. A critical role for muscle ring finger-1 in acute lung injury-associated skeletal muscle wasting. Am J Respir Crit Care Med 2012; 185(8): 825-834. https://doi.org/10.1164/rccm.201106-1150OC
- Sartori R, Milan G, Patron M, Mammucari C, Blaauw B, Abraham R, et al. Smad2 and 3 transcription factors control muscle mass in adulthood. Am J Physiol Cell Physiol 2009; 296(6): C1248-C1257. https://doi.org/10.1152/ajpcell.00104.2009
- Chen MM, Li Y, Deng SL, Zhao Y, Lian ZX, Yu K. Mitochondrial function and reactive oxygen/nitrogen species in skeletal muscle. Front Cell Dev Biol 2022; 10: 826981.
- Rahman FA, Quadrilatero J. Mitochondrial network remodeling: an important feature of myogenesis and skeletal muscle regeneration. Cell Mol Life Sci 2021; 78(10): 4653-4675. https://doi.org/10.1007/s00018-021-03807-9
- Chen TH, Koh KY, Lin KM, Chou CK. Mitochondrial dysfunction as an underlying cause of skeletal muscle disorders. Int J Mol Sci 2022; 23(21): 12926.
- Jang MK, Park C, Hong S, Li H, Rhee E, Doorenbos AZ. Skeletal muscle mass change during chemotherapy: a systematic review and meta-analysis. Anticancer Res 2020; 40(5): 2409-2418. https://doi.org/10.21873/anticanres.14210
- Barreto R, Waning DL, Gao H, Liu Y, Zimmers TA, Bonetto A. Chemotherapy-related cachexia is associated with mitochondrial depletion and the activation of ERK1/2 and p38 MAPKs. Oncotarget 2016; 7(28): 43442-43460. https://doi.org/10.18632/oncotarget.9779
- Furrer R, Handschin C. Muscle wasting diseases: novel targets and treatments. Annu Rev Pharmacol Toxicol 2019; 59(1): 315-339. https://doi.org/10.1146/annurev-pharmtox-010818-021041
- Lee H, Jeong JH, Hwang SH, Yeon SH, Ryu JH. A lignan from Alnus japonica activates myogenesis and alleviates dexamethasone-induced myotube atrophy. Planta Med 2023; 89(5): 484-492. https://doi.org/10.1055/a-1891-3366
- Zhang H, Chi M, Chen L, Sun X, Wan L, Yang Q, et al. Linalool prevents cisplatin induced muscle atrophy by regulating IGF-1/Akt/FoxO pathway. Front Pharmacol 2020; 11: 598166.
- Lee H, Heo JW, Kim AR, Kweon M, Nam S, Lim JS, et al. Z-ajoene from crushed garlic alleviates cancer-induced skeletal muscle atrophy. Nutrients 2019; 11(11): 2724.
- Zhang S, Chai X, Hou G, Zhao F, Meng Q. Platycodon grandiflorum (Jacq.) A. DC.: a review of phytochemistry, pharmacology, toxicology and traditional use. Phytomedicine 2022; 106: 154422.
- Seo YS, Kang OH, Kong R, Zhou T, Kim SA, Ryu S, et al. Polygalacin D induces apoptosis and cell cycle arrest via the PI3K/Akt pathway in non-small cell lung cancer. Oncol Rep 2018; 39(4): 1702-1710. https://doi.org/10.3892/or.2018.6230
- Nan F, Nan W, Yu Z, Wang H, Cui X, Jiang S, et al. Polygalacin D inhibits the growth of hepatocellular carcinoma cells through BNIP3L-mediated mitophagy and endogenous apoptosis pathways. Chin J Nat Med 2023; 21(5): 346-358. https://doi.org/10.1016/S1875-5364(23)60452-2
- Xiao S, Liu N, Yang X, Ji G, Li M. Polygalacin D suppresses esophageal squamous cell carcinoma growth and metastasis through regulating miR-142-5p/Nrf2 axis. Free Radic Biol Med 2021; 164: 58-75. https://doi.org/10.1016/j.freeradbiomed.2020.11.029
- Ishii H, Tori K, Tozyo T, Yoshimura Y. Saponins from roots of Platycodon grandiflorum. Part 2. Isolation and structure of new triterpene glycosides. J Chem Soc Perkin Trans 1 1984; 661-668.
- Yu J, Chang X, Peng H, Wang X, Wang J, Peng D, et al. A strategy based on isocratic and linear-gradient high-speed counter-current chromatography for the comprehensive separation of platycosides from Platycodi radix. Anal Methods 2021; 13(4): 477-483. https://doi.org/10.1039/D0AY02029J
- Le Grand F, Rudnicki MA. Skeletal muscle satellite cells and adult myogenesis. Curr Opin Cell Biol 2007; 19(6): 628-633. https://doi.org/10.1016/j.ceb.2007.09.012
- Mukund K, Subramaniam S. Skeletal muscle: a review of molecular structure and function, in health and disease. Wiley Interdiscip Rev Syst Biol Med 2020; 12(1): e1462.
- Sartori R, Romanello V, Sandri M. Mechanisms of muscle atrophy and hypertrophy: implications in health and disease. Nat Commun 2021; 12(1): 330.
- Yin L, Li N, Jia W, Wang N, Liang M, Yang X, et al. Skeletal muscle atrophy: from mechanisms to treatments. Pharmacol Res 2021; 172: 105807.
- Huo F, Liu Q, Liu H. Contribution of muscle satellite cells to sarcopenia. Front Physiol 2022; 13: 892749.
- Polen-De C, Giri S, Fadadu P, Weaver A, Mcgree ME, Moynagh M, et al. Muscle loss during cancer therapy is associated with poor outcomes in advanced ovarian cancer. J Natl Cancer Inst Monogr 2023; 2023(61): 43-48. https://doi.org/10.1093/jncimonographs/lgad007
- Blauwhoff-Buskermolen S, Versteeg KS, de van der Schueren MA, den Braver NR, Berkhof J, Langius JA, et al. Loss of muscle mass during chemotherapy is predictive for poor survival of patients with metastatic colorectal cancer. J Clin Oncol 2016; 34(12): 1339-1344. https://doi.org/10.1200/JCO.2015.63.6043
- Cespedes Feliciano EM, Lee VS, Prado CM, Meyerhardt JA, Alexeeff S, Kroenke CH, et al. Muscle mass at the time of diagnosis of nonmetastatic colon cancer and early discontinuation of chemotherapy, delays, and dose reductions on adjuvant FOLFOX: the C-SCANS study. Cancer 2017; 123(24): 4868-4877. https://doi.org/10.1002/cncr.30950
- Gouspillou G, Hepple RT. Editorial: mitochondria in skeletal muscle health, aging and diseases. Front Physiol 2016; 7: 446.
- Hood DA, Memme JM, Oliveira AN, Triolo M. Maintenance of skeletal muscle mitochondria in health, exercise, and aging. Annu Rev Physiol 2019; 81(1): 19-41. https://doi.org/10.1146/annurev-physiol-020518-114310
- Carter HN, Pauly M, Tryon LD, Hood DA. Effect of contractile activity on PGC-1α transcription in young and aged skeletal muscle. J Appl Physiol (1985) 2018; 124(6): 1605-1615. https://doi.org/10.1152/japplphysiol.01110.2017
- Bloemberg D, Quadrilatero J. Autophagy, apoptosis, and mitochondria: molecular integration and physiological relevance in skeletal muscle. Am J Physiol Cell Physiol 2019; 317(1): C111-C130. https://doi.org/10.1152/ajpcell.00261.2018
- Leduc-Gaudet JP, Hussain SN, Barreiro E, Gouspillou G. Mitochondrial dynamics and mitophagy in skeletal muscle health and aging. Int J Mol Sci 2021; 22(15): 8179.
- Jackson HE, Ingham PW. Control of muscle fibre-type diversity during embryonic development: the zebrafish paradigm. Mech Dev 2013; 130(9-10): 447-457. https://doi.org/10.1016/j.mod.2013.06.001
- Parsons MJ, Campos I, Hirst EM, Stemple DL. Removal of dystroglycan causes severe muscular dystrophy in zebrafish embryos. Development 2002; 129(14): 3505-3512. https://doi.org/10.1242/dev.129.14.3505