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New advances in drug development for metabolic dysfunction-associated diseases and alcohol-associated liver disease.
Zhang, Jinming; Li, Yixin; Yang, Liu; Ma, Ningning; Qian, Shengying; Chen, Yingfen; Duan, Yajun; Xiang, Xiaogang; He, Yong.
Afiliación
  • Zhang J; Department of Infectious Diseases, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200025, China.
  • Li Y; Department of Cardiology, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China (USTC), Hefei, 230001, Anhui, China.
  • Yang L; Shanghai Institute of Materia Medica (SIMM), Chinese Academy of Sciences, Shanghai, 201203, China.
  • Ma N; University of Chinese Academy of Sciences, Beijing, China.
  • Qian S; Shanghai Institute of Materia Medica (SIMM), Chinese Academy of Sciences, Shanghai, 201203, China.
  • Chen Y; University of Chinese Academy of Sciences, Beijing, China.
  • Duan Y; Shanghai Institute of Materia Medica (SIMM), Chinese Academy of Sciences, Shanghai, 201203, China.
  • Xiang X; University of Chinese Academy of Sciences, Beijing, China.
  • He Y; Shanghai Institute of Materia Medica (SIMM), Chinese Academy of Sciences, Shanghai, 201203, China.
Cell Biosci ; 14(1): 90, 2024 Jul 06.
Article en En | MEDLINE | ID: mdl-38971765
ABSTRACT
Metabolic disorders are currently threatening public health worldwide. Discovering new targets and developing promising drugs will reduce the global metabolic-related disease burden. Metabolic disorders primarily consist of lipid and glucose metabolic disorders. Specifically, metabolic dysfunction-associated steatosis liver disease (MASLD) and alcohol-associated liver disease (ALD) are two representative lipid metabolism disorders, while diabetes mellitus is a typical glucose metabolism disorder. In this review, we aimed to summarize the new drug candidates with promising efficacy identified in clinical trials for these diseases. These drug candidates may provide alternatives for patients with metabolic disorders and advance the progress of drug discovery for the large disease burden.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Cell Biosci Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Cell Biosci Año: 2024 Tipo del documento: Article País de afiliación: China