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Assessing Cellular Target Engagement by SHP2 (PTPN11) Phosphatase Inhibitors
Published on: July 17, 2020
Protein tyrosine phosphatase 1B (PTP1B) and obesity
1Department of Chemistry, Inha University, Incheon, Korea. hcho@inha.ac.kr
Abstract:
Protein tyrosine phosphatase 1B (PTP1B) is a negative regulator of the leptin and insulin signaling pathways. The important roles of PTP1B related to obesity and diabetes were confirmed by a deletion of PTP1B gene in mice. Mice with the whole body deletion of PTP1B were protected against the development of obesity and diabetes. When PTP1B gene was deleted selectively in the brain of mice, the major effects on weight and glucose control were consistent with the whole body deletion of PTP1B. This is in contrast to the muscle-, liver-, and adipocyte-specific deletion, which had no beneficial effects on obesity. While these results indicate the importance of neuronal PTP1B in maintaining energy homeostasis, the peripheral PTP1B is also being investigated for their potential roles in the control of energy balance. Validation of PTP1B as a therapeutic target for obesity and diabetes prompted efforts to develop potent and selective inhibitors of PTP1B. Among the small molecule inhibitors investigated, trodusquemine, which acts both centrally and peripherally, is currently in phase 2 clinical trials. An approach using PTP1B-directed antisense oligonucleotides is also in phase 2 clinical trials.
Insights
Protein tyrosine phosphatase 1B (PTP1B) regulates obesity and diabetes. Deleting the PTP1B gene in mouse brains protected against obesity and improved glucose control, highlighting its role in energy homeostasis.
Area of Science:
- Biochemistry
- Metabolism
- Neuroscience
Background:
- Protein tyrosine phosphatase 1B (PTP1B) negatively regulates insulin and leptin signaling pathways.
- Dysregulation of PTP1B is implicated in metabolic disorders like obesity and diabetes.
Purpose of the Study:
- To investigate the role of neuronal PTP1B in energy homeostasis.
- To evaluate the therapeutic potential of PTP1B inhibition for obesity and diabetes.
Main Methods:
- Gene deletion studies in mice (whole-body, brain-specific, and peripheral tissue-specific).
- Assessment of metabolic parameters including weight gain and glucose control.
- Investigation of small molecule inhibitors and antisense oligonucleotides targeting PTP1B.
Main Results:
- Whole-body PTP1B gene deletion protected mice against obesity and diabetes.
- Selective deletion of PTP1B in the brain mimicked the protective effects of whole-body deletion.
- Peripheral PTP1B deletion showed no significant beneficial effects on obesity.
Conclusions:
- Neuronal PTP1B plays a critical role in maintaining energy balance and glucose homeostasis.
- PTP1B is a validated therapeutic target for obesity and diabetes, with inhibitors in clinical development.
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