RAGE: A potential therapeutic target during FGF1 treatment of diabetes‐mediated liver injury

Author:

Zheng Peipei12,Tang Zonghao3,Xiong Jun1ORCID,Wang Beini1,Xu Jingyu2,Chen Lulu1,Cai Shufang2,Wu Chengbiao4,Ye Libing1,Xu Ke2ORCID,Chen Zimiao1,Wu Yanqing2ORCID,Xiao Jian1ORCID

Affiliation:

1. Department of Endocrinology The First Affiliated Hospital and School of Pharmaceutical Sciences Wenzhou Medical University Wenzhou China

2. The Institute of Life Sciences Wenzhou University Wenzhou China

3. Key Laboratory of Medical Electrophysiology of Ministry of Education Drug Discovery Research Center Southwest Medical University Luzhou China

4. Clinical Research Center Affiliated Xiangshan Hospital Wenzhou Medical University Wenzhou China

Funder

National Natural Science Foundation of China

Natural Science Foundation of Zhejiang Province

Publisher

Wiley

Subject

Cell Biology,Molecular Medicine

Reference42 articles.

1. In search of the optimal management strategy for non‐alcoholic fatty liver disease in type 2 diabetes;Lee CH;J Diabetes Investig,2020

2. Nonalcoholic fatty liver disease and chronic vascular complications of diabetes mellitus;Targher G;Nat Rev Endocrinol,2018

3. Progression of NAFLD to diabetes mellitus, cardiovascular disease or cirrhosis;Anstee QM;Nat Rev Gastroenterol Hepatol,2013

4. Role of advanced glycation end products in cellular signaling;Ott C;Redox Biol,2014

5. Advanced glycation endproducts trigger autophagy in cadiomyocyte via RAGE/PI3K/AKT/mTOR pathway;Hou X;Cardiovasc Diabetol,2014

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