ATR inhibition controls aggressive prostate tumors deficient in Y-linked histone demethylase KDM5D.
Ontology highlight
ABSTRACT: Epigenetic modifications control cancer development and clonal evolution in various cancer types. Here, we show that loss of the male-specific histone demethylase lysine-specific demethylase 5D (KDM5D) encoded on the Y chromosome epigenetically modifies histone methylation marks and alters gene expression, resulting in aggressive prostate cancer. Fluorescent in situ hybridization demonstrated that segmental or total deletion of the Y chromosome in prostate cancer cells is one of the causes of decreased KDM5D mRNA expression. The result of ChIP-sequencing analysis revealed that KDM5D preferably binds to promoter regions with coenrichment of the motifs of crucial transcription factors that regulate the cell cycle. Loss of KDM5D expression with dysregulated H3K4me3 transcriptional marks was a
SUBMITTER: Komura K
PROVIDER: S-EPMC6025984 | biostudies-literature | 2018 Jul
REPOSITORIES: biostudies-literature
ACCESS DATA