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Mol Cancer Res. 2015 Apr;13(4):636-50. doi: 10.1158/1541-7786.MCR-13-0268. Epub 2015 Feb 4.

The histone demethylase jumonji coordinates cellular senescence including secretion of neural stem cell-attracting cytokines.

Author information

1
Department of Neurosciences, City of Hope Beckman Research Institute and Medical Center, Duarte, California. Irell and Manella Graduate School of Biological Sciences, City of Hope Beckman Research Institute and Medical Center, Duarte, California.
2
Department of Neurosciences, City of Hope Beckman Research Institute and Medical Center, Duarte, California.
3
Bioinformatics Core Facility, City of Hope Beckman Research Institute and Medical Center, Duarte, California.
4
Department of Neurosciences, City of Hope Beckman Research Institute and Medical Center, Duarte, California. Division of Neurosurgery, City of Hope Beckman Research Institute and Medical Center, Duarte, California.
5
Department of Neurosciences, City of Hope Beckman Research Institute and Medical Center, Duarte, California. mbarish@coh.org.

Abstract

Jumonji domain-containing protein 3 (JMJD3/KDM6B) demethylates lysine 27 on histone H3 (H3K27me3), a repressive epigenetic mark controlling chromatin organization and cellular senescence. To better understand the functional consequences of JMJD3 its expression was investigated in brain tumor cells. Querying patient expression profile databases confirmed JMJD3 overexpression in high-grade glioma. Immunochemical staining of two glioma cell lines, U251 and U87, indicated intrinsic differences in JMJD3 expression levels that were reflected in changes in cell phenotype and variations associated with cellular senescence, including senescence-associated β-galactosidase (SA-β-gal) activity and the senescence-associated secretory phenotype (SASP). Overexpressing wild-type JMJD3 (JMJD3wt) activated SASP-associated genes, enhanced SA-β-gal activity, and induced nuclear blebbing. Conversely, overexpression of a catalytically inactive dominant negative mutant JMJD3 (JMJD3mut) increased proliferation. In addition, a large number of transcripts were identified by RNA-seq as altered in JMJD3 overexpressing cells, including cancer- and inflammation-related transcripts as defined by Ingenuity Pathway Analysis. These results suggest that expression of the SASP in the context of cancer undermines normal tissue homeostasis and contributes to tumorigenesis and tumor progression. These studies are therapeutically relevant because inflammatory cytokines have been linked to homing of neural stem cells and other stem cells to tumor loci.

IMPLICATIONS:

This glioma study brings together actions of a normal epigenetic mechanism (JMJD3 activity) with dysfunctional activation of senescence-related processes, including secretion of SASP proinflammatory cytokines and stem cell tropism toward tumors.

PMID:
25652587
PMCID:
PMC4844544
DOI:
10.1158/1541-7786.MCR-13-0268
[Indexed for MEDLINE]
Free PMC Article

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