Myostatin Research: From Molecular Understanding to Clinical Translation for Musculoskeletal and Metabolic Disorders
Myostatin (Mstn), a well-characterized member of the transforming growth factor-β (TGF-β) superfamily, serves as a key negative regulator of skeletal muscle mass. Its overactivation is closely associated with the pathogenesis of various musculoskeletal and metabolic disorders. Over the past decades, inhibiting Mstn has emerged as a promising therapeutic strategy to promote muscle growth. A range of Mstn-targeted inhibitors has been developed, yielding encouraging preclinical and clinical outcomes. These include small molecules, monoclonal antibodies, peptibodies, and gene therapy-based approaches. This review summarizes the biological structure and function of Mstn, provides a comprehensive overview of recent advances in Mstn-targeted therapeutics, and offers critical insights into future directions for drug development and clinical translation.
Authors
- Hewen Jiang (ORCID: https://orcid.org/0000-0001-5103-1681)
- Ge Zhang (ORCID: https://orcid.org/0000-0002-7807-7695)
- Shijian Ding
- Chong Gao
- Chongguang Lei
- Xin Yang
- Zongkang Zhang
- Yuanyuan Yu
- Bao-Ting Zhang
- Ling Qin (ORCID: https://orcid.org/0000-0001-6173-6167)
- Luyao Wang
- Aiping Lyu
Institutions
- Guangzhou University of Chinese Medicine (CN)
- Hong Kong Baptist University (HK)
- Chinese University of Hong Kong (HK)
Publication Details
- Journal
- International Journal of Molecular Sciences
- Published
- 2026-04-25
- DOI
- https://doi.org/10.3390/ijms27093836
- Primary Topic
- Muscle Physiology and Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Key Project of Research and Development Plan of Hunan Province
- Hong Kong Baptist University
- National Natural Science Foundation of China
- Innovation and Technology Commission
- Chinese University of Hong Kong
- Guangdong Science and Technology Department