Yeping Huang, Bin Liu, Cheng Hu, Yan Lu. Secreted proteins in treating metabolic dysfunction-associated steatotic liver disease: from bench towards bedside[J]. Protein&Cell, 2025, 16(8): 641-666. doi: 10.1093/procel/pwaf027
Citation: Yeping Huang, Bin Liu, Cheng Hu, Yan Lu. Secreted proteins in treating metabolic dysfunction-associated steatotic liver disease: from bench towards bedside[J]. Protein&Cell, 2025, 16(8): 641-666. doi: 10.1093/procel/pwaf027

Secreted proteins in treating metabolic dysfunction-associated steatotic liver disease: from bench towards bedside

  • Metabolic dysfunction-associated steatotic liver disease (MASLD) has become a global epidemic, yet effective pharmacological treatments remain limited. Secreted proteins play diverse roles in regulating glucose and lipid metabolism, and their dysregulation is implicated in the development of various metabolic diseases, including MASLD. Therefore, targeting secreted proteins and modulating associated signaling pathways represents a promising therapeutic strategy for MASLD. In this review, we summarize recent findings on the roles of emerging families of secreted proteins in MASLD and related metabolic disorders. These include the orosomucoid (ORM) family, secreted acidic cysteine rich glycoprotein (SPARC) family, neuregulin (Nrg) family, growth differentiation factor (GDF) family, interleukin (IL) family, fibroblast growth factor (FGF) family, bone morphogenic protein (BMP) family, as well as isthmin-1 (Ism1) and mesencephalic astrocyte-derived neurotrophic factor (MANF). The review highlights their impact on glucose and lipid metabolism and discusses the clinical potential of targeting these secreted proteins as a therapeutic approach for MASLD.
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