
doi: 10.4161/cc.1.1.95
pmid: 12429903
The MEK family of protein kinases plays key roles in regulating cellular responses to mitogens as well as environmental stress. Inappropriate activation of these kinases contributes to tumorigenesis. In contrast, anthrax lethal factor, the principal virulence factor of anthrax toxin, has been demonstrated to selectively inactivate MEKs. In this article we will discuss recent advances in our understanding of molecular aspects of the pathogenesis of anthrax, emphasizing the potential role of MEK signalling in this disease, and outline novel strategies to use anthrax lethal toxin in the treatment of cancer.
Mitogen-Activated Protein Kinase Kinases, Antigens, Bacterial, MAP Kinase Kinase 3, Bacterial Toxins, MAP Kinase Kinase 2, MAP Kinase Kinase 1, MAP Kinase Kinase 7, MAP Kinase Kinase 6, MAP Kinase Kinase 5, Protein Serine-Threonine Kinases, Protein-Tyrosine Kinases, Anthrax, Bacillus anthracis, Neoplasms, Calcium-Calmodulin-Dependent Protein Kinases, Animals, Humans, Signal Transduction
Mitogen-Activated Protein Kinase Kinases, Antigens, Bacterial, MAP Kinase Kinase 3, Bacterial Toxins, MAP Kinase Kinase 2, MAP Kinase Kinase 1, MAP Kinase Kinase 7, MAP Kinase Kinase 6, MAP Kinase Kinase 5, Protein Serine-Threonine Kinases, Protein-Tyrosine Kinases, Anthrax, Bacillus anthracis, Neoplasms, Calcium-Calmodulin-Dependent Protein Kinases, Animals, Humans, Signal Transduction
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