| Literature DB >> 31515251 |
Chun Shik Park1, Andrew H Lewis1,2, Taylor J Chen1,2, Cory S Bridges1, Ye Shen1,2, Koramit Suppipat3, Monica Puppi1, Julie A Tomolonis4, Paul D Pang2, Toni-Ann Mistretta1, Leyuan Ma5, Michael R Green5, Rachel Rau6, H Daniel Lacorazza1.
Abstract
Leukemia stem cells are a rare population with a primitive progenitor phenotype that can initiate, sustain, and recapitulate leukemia through a poorly understood mechanism of self-renewal. Here, we report that Krüppel-like factor 4 (KLF4) promotes disease progression in a murine model of chronic myeloid leukemia (CML)-like myeloproliferative neoplasia by repressing an inhibitory mechanism of preservation in leukemia stem/progenitor cells with leukemia-initiating capacity. Deletion of the Klf4 gene severely abrogated the maintenance of BCR-ABL1(p210)-induced CML by impairing survival and self-renewal in BCR-ABL1+ CD150+ lineage-negative Sca-1+ c-Kit+ leukemic cells. Mechanistically, KLF4 repressed the Dyrk2 gene in leukemic stem/progenitor cells; thus, loss of KLF4 resulted in elevated levels of dual-specificity tyrosine-(Y)-phosphorylation-regulated kinase 2 (DYRK2), which were associated with inhibition of survival and self-renewal via depletion of c-Myc protein and p53 activation. In addition to transcriptional regulation, stabilization of DYRK2 protein by inhibiting ubiquitin E3 ligase SIAH2 with vitamin K3 promoted apoptosis and abrogated self-renewal in murine and human CML stem/progenitor cells. Altogether, our results suggest that DYRK2 is a molecular checkpoint controlling p53- and c-Myc-mediated regulation of survival and self-renewal in CML cells with leukemic-initiating capacity that can be targeted with small molecules.Entities:
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Year: 2019 PMID: 31515251 PMCID: PMC6887114 DOI: 10.1182/blood.2018875922
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 25.476