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Regulation of Ku70-Bax Complex in Cells
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 deace...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Libertas Academica
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4167316/ https://www.ncbi.nlm.nih.gov/pubmed/25278782 http://dx.doi.org/10.4137/JCD.S13695 |
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author | Hada, Manila Kwok, Roland PS |
author_facet | Hada, Manila Kwok, Roland PS |
author_sort | Hada, Manila |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-4167316 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Libertas Academica |
record_format | MEDLINE/PubMed |
spelling | pubmed-41673162014-10-02 Regulation of Ku70-Bax Complex in Cells Hada, Manila Kwok, Roland PS J Cell Death Perspective 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. Libertas Academica 2014-02-13 /pmc/articles/PMC4167316/ /pubmed/25278782 http://dx.doi.org/10.4137/JCD.S13695 Text en © 2014 the author(s), publisher and licensee Libertas Academica Ltd. This is an open access article published under the Creative Commons CC-BY-NC 3.0 License. |
spellingShingle | Perspective Hada, Manila Kwok, Roland PS Regulation of Ku70-Bax Complex in Cells |
title | Regulation of Ku70-Bax Complex in Cells |
title_full | Regulation of Ku70-Bax Complex in Cells |
title_fullStr | Regulation of Ku70-Bax Complex in Cells |
title_full_unstemmed | Regulation of Ku70-Bax Complex in Cells |
title_short | Regulation of Ku70-Bax Complex in Cells |
title_sort | regulation of ku70-bax complex in cells |
topic | Perspective |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4167316/ https://www.ncbi.nlm.nih.gov/pubmed/25278782 http://dx.doi.org/10.4137/JCD.S13695 |
work_keys_str_mv | AT hadamanila regulationofku70baxcomplexincells AT kwokrolandps regulationofku70baxcomplexincells |