Cited by 645PI3K/AKT/mTOR signaling in cancerMetabolism, Diabetes, and CancerAutophagy in Disease and Therapy

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LKB1 and AMP-activated protein kinase control of mTOR signalling and growth

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Shaw, R. J.·2009·Acta Physiologica

DOI 10.1111/j.1748-1716.2009.01972.xPMC PMC2760308

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Abstract

The AMP-activated serine/threonine protein kinase (AMPK) is a sensor of cellular energy status found in all eukaryotes that is activated under conditions of low intracellular ATP following stresses such as nutrient deprivation or hypoxia. In the past 5 years, work from a large number of laboratories has revealed that one of the major downstream signalling pathways regulated by AMPK is the mammalian target-of-rapamycin [mammalian target of rapamycin (mTOR) pathway]. Interestingly, like AMPK, the mTOR serine/threonine kinase plays key roles not only in growth control and cell proliferation but also in metabolism. Recent work has revealed that across eukaryotes mTOR orthologues are found in two biochemically distinct complexes and only one of those complexes (mTORC1 in mammals) is acutely sensitive to rapamycin and regulated by nutrients and AMPK. Many details of the molecular mechanism by which AMPK inhibits mTORC1 signalling have also been decoded in the past 5 years. AMPK directly phosphorylates at least two proteins to induce rapid suppression of mTORC1 activity, the TSC2 tumour suppressor and the critical mTORC1 binding subunit raptor. Here we explore the molecular connections between AMPK and mTOR signalling pathways and examine the physiological processes in which AMPK regulation of mTOR is critical for growth or metabolic control. The functional conservation of AMPK and TOR in all eukaryotes, and the sequence conservation around the AMPK phosphorylation sites in raptor across all eukaryotes examined suggest that this represents a fundamental cell growth module connecting nutrient status to the cell growth machinery. These findings have broad implications for the control of cell growth by nutrients in a number of cellular and organismal contexts.

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Authors: Shaw, R. J.
Affiliations: Salk Institute for Biological Studies (US)
Corresponding author: Shaw, R. J.
ORCID: Shaw, R. J.
Venue: Acta Physiologica
Publisher: Wiley
Published: 2009-04
Volume: 196
Issue: 1
Pages: 65-80
ISSN: 1748-1708 (ISSN-L)
1748-1716
DOI: 10.1111/j.1748-1716.2009.01972.x
PMC: PMC2760308
OpenAlex: W2011239505
Cited by: 644
References: 143
Citations by year: 2026: 21 · 2025: 29 · 2024: 22 · 2023: 24 · 2022: 42 · 2021: 40 · 2020: 42 · 2019: 50 · 2018: 34 · 2017: 31 · 2016: 44 · 2015: 47 · 2014: 41 · 2013: 42 · 2012: 55
FWCI: 3.37
Type: journal article
Language: en
Open access: green
www.ncbi.nlm.nih.gov
Licence: onlinelibrary.wiley.com/termsAndConditions#vor (vor)
Locations: Acta Physiologica (publishedVersion)
PubMed (publishedVersion)
PubMed Central (acceptedVersion)
Funders: National Cancer Institute (P01CA120964)
National Institute of Diabetes and Digestive and Kidney Diseases (R01DK080425)
Topics: Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › PI3K/AKT/mTOR signaling in cancer
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
Keywords: LKB1, AMPK, mTOR signaling, mTORC1, raptors, TSC2, cell growth regulation, nutrient sensing, energy status, protein phosphorylation, rapamycin sensitivity, cell proliferation, metabolism
MeSH terms: Mechanistic Target of Rapamycin Complex 1, Regulatory-Associated Protein of mTOR, Tuberous Sclerosis Complex 2 Protein, AMP-Activated Protein Kinase Kinases, Aging, Animals, Antibiotics, Antineoplastic, Autophagy, Clinical Trials as Topic, Energy Metabolism, Humans, Neoplasms, Proteins, Transcription Factors, Signal Transduction, Protein Serine-Threonine Kinases, Sirolimus, Tumor Suppressor Proteins, Multiprotein Complexes, Intracellular Signaling Peptides and Proteins, Adaptor Proteins, Signal Transducing, AMP-Activated Protein Kinases, TOR Serine-Threonine Kinases

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LKB1 and AMP-activated protein kinase control of mTOR signalling and growth

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