| Literature DB >> 12879020 |
James Spicer1, Sydonia Rayter, Neville Young, Richard Elliott, Alan Ashworth, Darrin Smith.
Abstract
Loss-of-function mutations in the LKB1 (STK11) serine-threonine kinase gene cause Peutz-Jeghers syndrome, which is associated with inherited susceptibility to colorectal and other cancers. No downstream targets of LKB1 kinase activity have been identified. Here we show that LKB1 can direct the phosphorylation of the serine-threonine kinase PAR1A. The amino-acid residues phosphorylated as a result of LKB1 activity have been identified and phosphorylation at these residues is required for PAR1A kinase activity. PAR1A has previously been implicated as a positive regulator of the Wnt-betacatenin signalling pathway. We show here that LKB1 can modify transcription driven by the Wnt-regulated TCF response element, implicating LKB1 in a pathway known to play a key role in human colorectal tumorigenesis.Entities:
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Year: 2003 PMID: 12879020 DOI: 10.1038/sj.onc.1206669
Source DB: PubMed Journal: Oncogene ISSN: 0950-9232 Impact factor: 9.867