JANOVSKÁ, Pavlína, Emmanuel NORMANT, Hari MISKIN and Vítězslav BRYJA. Targeting Casein Kinase 1 (CK1) in Hematological Cancers. International Journal of Molecular Sciences. Basel: MDPI, 2020, vol. 21, No 23, p. 1-19. ISSN 1422-0067. Available from: https://dx.doi.org/10.3390/ijms21239026.
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Basic information
Original name Targeting Casein Kinase 1 (CK1) in Hematological Cancers
Authors JANOVSKÁ, Pavlína (203 Czech Republic, guarantor, belonging to the institution), Emmanuel NORMANT, Hari MISKIN and Vítězslav BRYJA (203 Czech Republic, belonging to the institution).
Edition International Journal of Molecular Sciences, Basel, MDPI, 2020, 1422-0067.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10608 Biochemistry and molecular biology
Country of publisher Switzerland
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 5.923
RIV identification code RIV/00216224:14310/20:00114621
Organization unit Faculty of Science
Doi http://dx.doi.org/10.3390/ijms21239026
UT WoS 000597481100001
Keywords in English casein kinase 1; CK1 alpha CK1 epsilon leukemia; CLL; AML; MM; inhibitors; umbralisib; WNT pathway
Tags rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Marie Šípková, DiS., učo 437722. Changed: 31/8/2021 16:26.
Abstract
The casein kinase 1 enzymes (CK1) form a family of serine/threonine kinases with seven CK1 isoforms identified in humans. The most important substrates of CK1 kinases are proteins that act in the regulatory nodes essential for tumorigenesis of hematological malignancies. Among those, the most important are the functions of CK1s in the regulation of Wnt pathways, cell proliferation, apoptosis and autophagy. In this review we summarize the recent developments in the understanding of biology and therapeutic potential of the inhibition of CK1 isoforms in the pathogenesis of chronic lymphocytic leukemia (CLL), other non-Hodgkin lymphomas (NHL), myelodysplastic syndrome (MDS), acute myeloid leukemia (AML) and multiple myeloma (MM). CK1 delta/epsilon inhibitors block CLL development in preclinical models via inhibition of WNT-5A/ROR1-driven non-canonical Wnt pathway. While no selective CK1 inhibitors have reached clinical stage to date, one dual PI3K delta and CK1 epsilon inhibitor, umbralisib, is currently in clinical trials for CLL and NHL patients. In MDS, AML and MM, inhibition of CK1 alpha, acting via activation of p53 pathway, showed promising preclinical activities and the first CK1 alpha inhibitor has now entered the clinical trials.
Links
EF16_025/0007381, research and development projectName: Preklinická progrese nových organických sloučenin s cílenou biologickou aktivitou
GX19-28347X, research and development projectName: Molekulární a funkční analýza biologie kasein kinázy 1
Investor: Czech Science Foundation
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