GDF15 Analogues Acting as GFRAL Ligands

GDF15型 恶病质 受体 能量稳态 厌食症 信号转导 生物 疾病 癌症 医学 内分泌学 内科学 细胞生物学
作者
Andrea Di Santo,Livio Tarchi,Gianluca Villa,Giovanni Castellini,Valdo Ricca,Roberta Squecco,Anna Maria Papini,Feliciana Real‐Fernández,Paolo Rovero
出处
期刊:ChemMedChem [Wiley]
标识
DOI:10.1002/cmdc.202400961
摘要

Growth differentiation factor 15 (GDF15) is a TGF‐β superfamily member involved in diverse physiological and pathological processes. It is expressed in various tissues and its circulating levels rise during exercise, aging, pregnancy, and conditions such as cancer, cardiovascular disease, and infections. The biological activities of GDF15, including anorexia and cachexia, are primarily mediated through the GFRAL receptor, localized in the brainstem and functioning via RET co‐receptor recruitment. This signaling is crucial for energy homeostasis and nausea induction. Recent studies suggest a broader GFRAL distribution, potentially explaining GDF15's distinct roles. These findings sparked interest in leveraging GDF15‐GFRAL pathways for therapeutic development. Two primary strategies include GDF15 analogues as GFRAL agonists for obesity treatment and GDF15‐derived peptides as antagonists to counteract cancer‐induced cachexia and related disorders. This review highlights advancements in understanding GDF15‐GFRAL signaling and its implications, summarizing bioactive GDF15‐derived molecules, their pharmacological applications, and offering insights into novel treatment avenues for GDF15‐associated conditions.

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