Targeting mTOR Signaling in Type 2 Diabetes Mellitus and Diabetes Complications

Author:

Yang Lin1,Zhang Zhixin1,Wang Doudou1,Jiang Yu2,Liu Ying1ORCID

Affiliation:

1. School of Life Sciences, Beijing University of Chinese Medicine, Beijing 102488, China

2. Department of Pharmacology and Chemical Biology, University of Pittsburgh School of Medicine, Pittsburgh PA15261, USA

Abstract

Abstract: The mechanistic target of rapamycin (mTOR) is a pivotal regulator of cell metabolism and growth. In the form of two different multi-protein complexes, mTORC1 and mTORC2, mTOR integrates cellular energy, nutrient and hormonal signals to regulate cellular metabolic homeostasis. In type 2 diabetes mellitus (T2DM), pathological conditions and end-organ complications can be attributed to aberrant mTOR. Substantial evidence suggests that two mTOR-mediated signaling schemes, mTORC1-p70S6 kinase 1 (S6K1) and mTORC2-protein kinase B (AKT), play a critical role in insulin sensitivity and that their dysfunction contributes to the development of T2DM. This review summarizes our current understanding of the role of mTOR signaling in T2DM and its associated complications, as well as the potential use of mTOR inhibitors in the treatment of T2DM.

Publisher

Bentham Science Publishers Ltd.

Subject

Clinical Biochemistry,Drug Discovery,Pharmacology,Molecular Medicine

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