Regulation of Ku70-Bax Complex in Cells
Author(s) -
Manila Hada,
Roland P.S. Kwok
Publication year - 2014
Publication title -
journal of cell death
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.419
H-Index - 15
ISSN - 1179-0660
DOI - 10.4137/jcd.s13695
Subject(s) - ku70 , programmed cell death , acetylation , apoptosis , microbiology and biotechnology , histone , hdac6 , cancer research , histone deacetylase , dna repair , chemistry , biology , dna , biochemistry , gene
Ku70, a DNA repair factor in the nucleus, also regulates cell death by binding to the apoptotic protein Bax in the cytoplasm. Acetylation of Ku70 triggers Bax release resulting in Bax dependent cell death. Thus dissociating Bax from Ku70, either by inhibiting histone deacetylase 6 (HDAC6) that deacetylates Ku70 or by increasing Ku70 acetylation induces cell death. Our results showed that in neuroblastoma cells, the depletion of Ku70 results in Bax-dependent cell death. This model provides a rationale for screening Ku70 acetylation modulators that can be tested in clinical trials, either alone or in combination with radiotherapy or DNA-damaging agents for the treatment of cancer.
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