Background: Protein kinase MELK is expressed at very high levels in glioblastomas, but it is not understood how this benefits tumor growth. Results: A deficiency of MELK causes replication stress and is associated with cell cycle arrest and senescence. Conclusion: MELK is required for progression through unperturbed S phase. Significance: The inhibition of MELK emerges as an attractive cancer therapy. © 2013 by The American Society for Biochemistry and Molecular Biology, Inc.
CITATION STYLE
Kig, C., Beullens, M., Beke, L., Van Eynde, A., Linders, J. T., Brehmer, D., & Bollen, M. (2013, August 16). Maternal embryonic leucine zipper kinase (MELK) reduces replication stress in glioblastoma cells. Journal of Biological Chemistry. American Society for Biochemistry and Molecular Biology Inc. https://doi.org/10.1074/jbc.M113.471433
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