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Cited by 560

The DOI matches its Crossref record; 5 of the 5 references it cites were found in a registry or an index.

Regulation of the TSC pathway by LKB1: evidence of a molecular link between tuberous sclerosis complex and Peutz-Jeghers syndrome

Open access
Corradetti, Michael N., Inoki, Ken, Bardeesy, Nabeel, DePinho, Ronald A., Guan, Kun-Liang·2004·Genes & Development

Abstract

Tuberous sclerosis complex (TSC) and Peutz-Jeghers syndrome (PJS) are dominantly inherited benign tumor syndromes that share striking histopathological similarities. Here we show that LKB1 , the gene mutated in PJS, acts as a tumor suppressor by activating TSC2 , the gene mutated in TSC. Like TSC2, LKB1 inhibits the phosphorylation of the key translational regulators S6K and 4EBP1. Furthermore, we show that LKB1 activates TSC2 through the AMP-dependent protein kinase (AMPK), indicating that LKB1 plays a role in cell growth regulation in response to cellular energy levels. Our results suggest that PJS and other benign tumor syndromes could be caused by dysregulation of the TSC2/mTOR pathway.

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Metadata

Authors
Corradetti, M. N., Inoki, K., Bardeesy, N., DePinho, R. A., & Guan, K.-L.
Venue
Genes & Development
Published
2004-07-01
Volume
18
Issue
13
Pages
1533-1538
ISSN
  • 0890-9369 (ISSN-L)
  • 1549-5477
OpenAlex
W2086589626
Cited by
560
References
5
Type
posted content
Language
en
Open access
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