MiRNA expression profiling of NB4 control cells versus NB4 cells treated with SAHA (Vorinostat)
Ontology highlight
ABSTRACT:
ORGANISM(S): Homo sapiens
SUBMITTER: carmela dell'aversana
PROVIDER: E-GEOD-37374 | biostudies-arrayexpress |
REPOSITORIES: biostudies-arrayexpress
Publications
HDAC inhibitors repress BARD1 isoform expression in acute myeloid leukemia cells via activation of miR-19a and/or b.
Lepore Ilaria I Dell'Aversana Carmela C Pilyugin Maxim M Conte Mariarosaria M Nebbioso Angela A De Bellis Floriana F Tambaro Francesco P FP Izzo Tiziana T Garcia-Manero Guillermo G Ferrara Felicetto F Irminger-Finger Irmgard I Altucci Lucia L
PloS one 20131211 12
Over the past years BARD1 (BRCA1-associated RING domain 1) has been considered as both a BRCA1 (BReast Cancer susceptibility gene 1, early onset) interactor and tumor suppressor gene mutated in breast and ovarian cancers. Despite its role as a stable heterodimer with BRCA1, increasing evidence indicates that BARD1 also has BRCA1-independent oncogenic functions. Here, we investigate BARD1 expression and function in human acute myeloid leukemias and its modulation by epigenetic mechanism(s) and mi ...[more]
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Project description:For a long time, the BARD1 (BRCA1-associated RING domain 1) protein has been considered as a BRCA1 (BReast Cancer susceptibility gene 1, early onset) interactor, and tumor suppressor mutated in breast and ovarian cancers. Despite its functions in a stable heterodimer with BRCA1, there is increasing evidence for BRCA1-independent functions of BARD1. Here, we investigated BARD1 expression and function in human acute myeloid leukemias and their modulation by epigenetic mechanisms and microRNA. We show that the HDACi (histone deacetylase inhibitor) Vorinostat reduces BARD1 mRNA levels by increasing miR-19a and miR-19b expression levels. Moreover, we identify specific BARD1 isoforms that might act as tumor diagnostic and prognostic markers.
2014-12-22 | GSE37374 | GEO
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