Histone deacetylase inhibitors and mithramycin a impact a similar neuroprotective pathway at a crossroad between cancer and neurodegeneration

Mithramycin A (MTM) and histone deacetylase inhibitors (HDACi) are effective therapeutic agents for cancer and neurodegenerative diseases. MTM is a FDA approved aureolic acid-type antibiotic that binds to GC-rich DNA sequences and interferes with Sp1 transcription factor binding to its target sites...

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Main Author: Sleiman, Sama F. (author)
Other Authors: Berlin, Jill (author), Basso, Manuela (author), Karuppagounder, Saravanan S. (author), Rohr, Jurgen (author), Ratan, Rajiv R. (author)
Format: article
Published: 2011
Online Access:http://hdl.handle.net/10725/6140
http://dx.doi.org/10.3390/ph4081183
http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php
http://www.mdpi.com/1424-8247/4/8/1183/htm
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author Sleiman, Sama F.
author2 Berlin, Jill
Basso, Manuela
Karuppagounder, Saravanan S.
Rohr, Jurgen
Ratan, Rajiv R.
author2_role author
author
author
author
author
author_facet Sleiman, Sama F.
Berlin, Jill
Basso, Manuela
Karuppagounder, Saravanan S.
Rohr, Jurgen
Ratan, Rajiv R.
author_role author
dc.creator.none.fl_str_mv Sleiman, Sama F.
Berlin, Jill
Basso, Manuela
Karuppagounder, Saravanan S.
Rohr, Jurgen
Ratan, Rajiv R.
dc.date.none.fl_str_mv 2011
2017-09-06T07:26:12Z
2017-09-06T07:26:12Z
2017-10-12
dc.identifier.none.fl_str_mv 1424-8247
http://hdl.handle.net/10725/6140
http://dx.doi.org/10.3390/ph4081183
Sleiman, S. F., Berlin, J., Basso, M., S Karuppagounder, S., Rohr, J., & Ratan, R. R. (2011). Histone deacetylase inhibitors and mithramycin A impact a similar neuroprotective pathway at a crossroad between cancer and neurodegeneration. Pharmaceuticals, 4(8), 1183-1195.
http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php
http://www.mdpi.com/1424-8247/4/8/1183/htm
dc.language.none.fl_str_mv en
dc.relation.none.fl_str_mv Pharmaceuticals
dc.rights.*.fl_str_mv info:eu-repo/semantics/openAccess
dc.title.none.fl_str_mv Histone deacetylase inhibitors and mithramycin a impact a similar neuroprotective pathway at a crossroad between cancer and neurodegeneration
dc.type.none.fl_str_mv Article
info:eu-repo/semantics/publishedVersion
info:eu-repo/semantics/article
description Mithramycin A (MTM) and histone deacetylase inhibitors (HDACi) are effective therapeutic agents for cancer and neurodegenerative diseases. MTM is a FDA approved aureolic acid-type antibiotic that binds to GC-rich DNA sequences and interferes with Sp1 transcription factor binding to its target sites (GC box). HDACi, on the other hand, modulate the activity of class I and II histone deacetylases. They mediate their protective function, in part, by regulating the acetylation status of histones or transcription factors, including Sp1, and in turn chromatin accessibility to the transcriptional machinery. Because these two classes of structurally and functionally diverse compounds mediate similar therapeutic functions, we investigated whether they act on redundant or synergistic pathways to protect neurons from oxidative death. Non-protective doses of each of the drugs do not synergize to create resistance to oxidative death suggesting that these distinct agents act via a similar pathway. Accordingly, we found that protection by MTM and HDACi is associated with diminished expression of the oncogene, Myc and enhanced expression of a tumor suppressor, p21waf1/cip1. We also find that neuroprotection by MTM or Myc knockdown is associated with downregulation of class I HDAC levels. Our results support a model in which the established antitumor drug MTM or canonical HDACi act via distinct mechanisms to converge on the downregulation of HDAC levels or activity respectively. These findings support the conclusion that an imbalance in histone acetylase and HDAC activity in favor of HDACs is key not only for oncogenic transformation, but also neurodegeneration.
eu_rights_str_mv openAccess
format article
id LAURepo_11aaae6b87ea90542a60dcae2d779752
identifier_str_mv 1424-8247
Sleiman, S. F., Berlin, J., Basso, M., S Karuppagounder, S., Rohr, J., & Ratan, R. R. (2011). Histone deacetylase inhibitors and mithramycin A impact a similar neuroprotective pathway at a crossroad between cancer and neurodegeneration. Pharmaceuticals, 4(8), 1183-1195.
language_invalid_str_mv en
network_acronym_str LAURepo
network_name_str Lebanese American University repository
oai_identifier_str oai:laur.lau.edu.lb:10725/6140
publishDate 2011
repository.mail.fl_str_mv
repository.name.fl_str_mv
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spelling Histone deacetylase inhibitors and mithramycin a impact a similar neuroprotective pathway at a crossroad between cancer and neurodegenerationSleiman, Sama F.Berlin, JillBasso, ManuelaKaruppagounder, Saravanan S.Rohr, JurgenRatan, Rajiv R.Mithramycin A (MTM) and histone deacetylase inhibitors (HDACi) are effective therapeutic agents for cancer and neurodegenerative diseases. MTM is a FDA approved aureolic acid-type antibiotic that binds to GC-rich DNA sequences and interferes with Sp1 transcription factor binding to its target sites (GC box). HDACi, on the other hand, modulate the activity of class I and II histone deacetylases. They mediate their protective function, in part, by regulating the acetylation status of histones or transcription factors, including Sp1, and in turn chromatin accessibility to the transcriptional machinery. Because these two classes of structurally and functionally diverse compounds mediate similar therapeutic functions, we investigated whether they act on redundant or synergistic pathways to protect neurons from oxidative death. Non-protective doses of each of the drugs do not synergize to create resistance to oxidative death suggesting that these distinct agents act via a similar pathway. Accordingly, we found that protection by MTM and HDACi is associated with diminished expression of the oncogene, Myc and enhanced expression of a tumor suppressor, p21waf1/cip1. We also find that neuroprotection by MTM or Myc knockdown is associated with downregulation of class I HDAC levels. Our results support a model in which the established antitumor drug MTM or canonical HDACi act via distinct mechanisms to converge on the downregulation of HDAC levels or activity respectively. These findings support the conclusion that an imbalance in histone acetylase and HDAC activity in favor of HDACs is key not only for oncogenic transformation, but also neurodegeneration.PublishedN/A2017-09-06T07:26:12Z2017-09-06T07:26:12Z20112017-10-12Articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1424-8247http://hdl.handle.net/10725/6140http://dx.doi.org/10.3390/ph4081183Sleiman, S. F., Berlin, J., Basso, M., S Karuppagounder, S., Rohr, J., & Ratan, R. R. (2011). Histone deacetylase inhibitors and mithramycin A impact a similar neuroprotective pathway at a crossroad between cancer and neurodegeneration. Pharmaceuticals, 4(8), 1183-1195.http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.phphttp://www.mdpi.com/1424-8247/4/8/1183/htmenPharmaceuticalsinfo:eu-repo/semantics/openAccessoai:laur.lau.edu.lb:10725/61402021-03-19T10:00:49Z
spellingShingle Histone deacetylase inhibitors and mithramycin a impact a similar neuroprotective pathway at a crossroad between cancer and neurodegeneration
Sleiman, Sama F.
status_str publishedVersion
title Histone deacetylase inhibitors and mithramycin a impact a similar neuroprotective pathway at a crossroad between cancer and neurodegeneration
title_full Histone deacetylase inhibitors and mithramycin a impact a similar neuroprotective pathway at a crossroad between cancer and neurodegeneration
title_fullStr Histone deacetylase inhibitors and mithramycin a impact a similar neuroprotective pathway at a crossroad between cancer and neurodegeneration
title_full_unstemmed Histone deacetylase inhibitors and mithramycin a impact a similar neuroprotective pathway at a crossroad between cancer and neurodegeneration
title_short Histone deacetylase inhibitors and mithramycin a impact a similar neuroprotective pathway at a crossroad between cancer and neurodegeneration
title_sort Histone deacetylase inhibitors and mithramycin a impact a similar neuroprotective pathway at a crossroad between cancer and neurodegeneration
url http://hdl.handle.net/10725/6140
http://dx.doi.org/10.3390/ph4081183
http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php
http://www.mdpi.com/1424-8247/4/8/1183/htm