| Literature DB >> 25242043 |
Rebekka K Schneider1, Vera Ademà2, Dirk Heckl1, Marcus Järås1, Mar Mallo3, Allegra M Lord1, Lisa P Chu1, Marie E McConkey1, Rafael Kramann4, Ann Mullally1, Rafael Bejar5, Francesc Solé3, Benjamin L Ebert6.
Abstract
The casein kinase 1A1 gene (CSNK1A1) is a putative tumor suppressor gene located in the common deleted region for del(5q) myelodysplastic syndrome (MDS). We generated a murine model with conditional inactivation of Csnk1a1 and found that Csnk1a1 haploinsufficiency induces hematopoietic stem cell expansion and a competitive repopulation advantage, whereas homozygous deletion induces hematopoietic stem cell failure. Based on this finding, we found that heterozygous inactivation of Csnk1a1 sensitizes cells to a CSNK1 inhibitor relative to cells with two intact alleles. In addition, we identified recurrent somatic mutations in CSNK1A1 on the nondeleted allele of patients with del(5q) MDS. These studies demonstrate that CSNK1A1 plays a central role in the biology of del(5q) MDS and is a promising therapeutic target.Entities:
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Year: 2014 PMID: 25242043 PMCID: PMC4199102 DOI: 10.1016/j.ccr.2014.08.001
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743