Unknown

Dataset Information

0

The tumor suppressor LKB1 kinase directly activates AMP-activated kinase and regulates apoptosis in response to energy stress.


ABSTRACT: AMP-activated protein kinase (AMPK) is a highly conserved sensor of cellular energy status found in all eukaryotic cells. AMPK is activated by stimuli that increase the cellular AMP/ATP ratio. Essential to activation of AMPK is its phosphorylation at Thr-172 by an upstream kinase, AMPKK, whose identity in mammalian cells has remained elusive. Here we present biochemical and genetic evidence indicating that the LKB1 serine/threonine kinase, the gene inactivated in the Peutz-Jeghers familial cancer syndrome, is the dominant regulator of AMPK activation in several mammalian cell types. We show that LKB1 directly phosphorylates Thr-172 of AMPKalpha in vitro and activates its kinase activity. LKB1-deficient murine embryonic fibroblasts show nearly complete loss of Thr-172 phosphorylation and downstream AMPK signaling in response to a variety of stimuli that activate AMPK. Reintroduction of WT, but not kinase-dead, LKB1 into these cells restores AMPK activity. Furthermore, we show that LKB1 plays a biologically significant role in this pathway, because LKB1-deficient cells are hypersensitive to apoptosis induced by energy stress. On the basis of these results, we propose a model to explain the apparent paradox that LKB1 is a tumor suppressor, yet cells lacking LKB1 are resistant to cell transformation by conventional oncogenes and are sensitive to killing in response to agents that elevate AMP. The role of LKB1/AMPK in the survival of a subset of genetically defined tumor cells may provide opportunities for cancer therapeutics.

SUBMITTER: Shaw RJ 

PROVIDER: S-EPMC373461 | biostudies-literature | 2004 Mar

REPOSITORIES: biostudies-literature

altmetric image

Publications

The tumor suppressor LKB1 kinase directly activates AMP-activated kinase and regulates apoptosis in response to energy stress.

Shaw Reuben J RJ   Kosmatka Monica M   Bardeesy Nabeel N   Hurley Rebecca L RL   Witters Lee A LA   DePinho Ronald A RA   Cantley Lewis C LC  

Proceedings of the National Academy of Sciences of the United States of America 20040225 10


AMP-activated protein kinase (AMPK) is a highly conserved sensor of cellular energy status found in all eukaryotic cells. AMPK is activated by stimuli that increase the cellular AMP/ATP ratio. Essential to activation of AMPK is its phosphorylation at Thr-172 by an upstream kinase, AMPKK, whose identity in mammalian cells has remained elusive. Here we present biochemical and genetic evidence indicating that the LKB1 serine/threonine kinase, the gene inactivated in the Peutz-Jeghers familial cance  ...[more]

Similar Datasets

| S-EPMC3399766 | biostudies-literature
| S-EPMC1859937 | biostudies-literature
| S-EPMC3977597 | biostudies-literature
| S-EPMC3496153 | biostudies-literature
| S-EPMC3210354 | biostudies-literature
| S-EPMC5826329 | biostudies-literature
| S-EPMC5615778 | biostudies-literature
| S-EPMC3279556 | biostudies-literature
| S-EPMC3866127 | biostudies-literature
| S-EPMC4003022 | biostudies-other