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mTOR: from growth signal integration to cancer, diabetes and ageing
Roberto Zoncu1, Alejo Efeyan, David M Sabatini
1Whitehead Institute for Biomedical Research, Nine Cambridge Center, Cambridge, Massachusetts 02142, USA.
Abstract:
In all eukaryotes, the target of rapamycin (TOR) signalling pathway couples energy and nutrient abundance to the execution of cell growth and division, owing to the ability of TOR protein kinase to simultaneously sense energy, nutrients and stress and, in metazoans, growth factors. Mammalian TOR complex 1 (mTORC1) and mTORC2 exert their actions by regulating other important kinases, such as S6 kinase (S6K) and Akt. In the past few years, a significant advance in our understanding of the regulation and functions of mTOR has revealed the crucial involvement of this signalling pathway in the onset and progression of diabetes, cancer and ageing.
Insights
The target of rapamycin (TOR) pathway links nutrient availability to cell growth. Understanding mTOR signaling is key to diseases like cancer, diabetes, and aging.
Area of Science:
- Cell Biology
- Biochemistry
- Molecular Biology
Background:
- The target of rapamycin (TOR) signaling pathway is a central regulator of cell growth and division in eukaryotes.
- TOR integrates signals of energy, nutrient, and stress levels, and growth factors in metazoans.
- Mammalian TOR complexes (mTORC1 and mTORC2) regulate key kinases like S6 kinase (S6K) and Akt.
Purpose of the Study:
- To elucidate the regulatory mechanisms and diverse functions of the TOR signaling pathway.
- To highlight the critical role of mTOR in the pathogenesis of major diseases.
Main Methods:
- The abstract does not specify methods.
Main Results:
- The abstract does not specify results.
Conclusions:
- Advances in understanding mTOR signaling have revealed its crucial involvement in the onset and progression of diabetes, cancer, and aging.
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