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Effects of acute doxorubicin treatment on hepatic proteome lysine acetylation status and the apoptotic environment.
| Content Provider | Europe PMC |
|---|---|
| Author | Dirks-Naylor, Amie J Kouzi, Samir A Bero, Joseph D Tran, Ngan TK Yang, Sendra Mabolo, Raean |
| Copyright Year | 2014 |
| Abstract | AIM: To determine if doxorubicin (Dox) alters hepatic proteome acetylation status and if acetylation status was associated with an apoptotic environment. METHODS: Doxorubicin (20 mg/kg; Sigma, Saint Louis, MO; n = 8) or NaCl (0.9%; n = 7) was administered as an intraperitoneal injection to male F344 rats, 6-wk of age. Once animals were treated with Dox or saline, all animals were fasted until sacrifice 24 h later. RESULTS: Dox treatment decreased proteome lysine acetylation likely due to a decrease in histone acetyltransferase activity. Proteome deacetylation may likely not be associated with a proapoptotic environment. Dox did not increase caspase-9, -8, or -3 activation nor poly (adenosine diphosphate-ribose) polymerase-1 cleavage. Dox did stimulate caspase-12 activation, however, it likely did not play a role in apoptosis induction. CONCLUSION: Early effects of Dox involve hepatic proteome lysine deacetylation and caspase-12 activation under these experimental conditions. |
| Related Links | https://europepmc.org/backend/ptpmcrender.fcgi?accid=PMC4160530&blobtype=pdf |
| ISSN | 19498454 |
| Volume Number | 5 |
| DOI | 10.4331/wjbc.v5.i3.377 |
| PubMed Central reference number | PMC4160530 |
| Issue Number | 3 |
| PubMed reference number | 25225604 |
| Journal | World Journal of Biological Chemistry [World J Biol Chem] |
| e-ISSN | 19498454 |
| Language | English |
| Publisher | Baishideng Publishing Group Inc |
| Publisher Date | 2014-08-01 |
| Access Restriction | Open |
| Rights License | ©2014 Baishideng Publishing Group Inc. All rights reserved. |
| Subject Keyword | Sirtuin 1 Sirtuin 3 Caspase Apoptosis Acetylation Histone deacetylase Histone acetyltransferase |
| Content Type | Text |
| Resource Type | Article |
| Subject | Biochemistry (medical) |