| Literature DB >> 26412324 |
Miguel Gallardo1, Hun Ju Lee2, Xiaorui Zhang1, Carlos Bueso-Ramos3, Laura R Pageon4, Mark McArthur4, Asha Multani5, Aziz Nazha1, Taghi Manshouri1, Jan Parker-Thornburg5, Inmaculada Rapado6, Alfonso Quintas-Cardama1, Steven M Kornblau1, Joaquin Martinez-Lopez6, Sean M Post7.
Abstract
hnRNP K regulates cellular programs, and changes in its expression and mutational status have been implicated in neoplastic malignancies. To directly examine its role in tumorigenesis, we generated a mouse model harboring an Hnrnpk knockout allele (Hnrnpk(+/-)). Hnrnpk haploinsufficiency resulted in reduced survival, increased tumor formation, genomic instability, and the development of transplantable hematopoietic neoplasms with myeloproliferation. Reduced hnRNP K expression attenuated p21 activation, downregulated C/EBP levels, and activated STAT3 signaling. Additionally, analysis of samples from primary acute myeloid leukemia patients harboring a partial deletion of chromosome 9 revealed a significant decrease in HNRNPK expression. Together, these data implicate hnRNP K in the development of hematological disorders and suggest hnRNP K acts as a tumor suppressor.Entities:
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Year: 2015 PMID: 26412324 PMCID: PMC4652598 DOI: 10.1016/j.ccell.2015.09.001
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743