Date of Award
1-1-2014
Language
English
Document Type
Dissertation
Degree Name
Doctor of Philosophy (PhD)
College/School/Department
Department of Biomedical Sciences
Content Description
1 online resource (xvii, 227 pages) : color illustrations.
Dissertation/Thesis Chair
Martin P Tenniswood
Committee Members
JoEllen Welsh, Douglas S Conklin, Thomas J Begley, Jason I Herschkowitz
Keywords
Epigenetic Therapy, Histone Deacetylase, Histone Deacetylase Inhibitor, Inflammatory Breast Cancer, Breast, Histone deacetylase, Enzyme inhibitors, Carcinogenesis
Subject Categories
Biology | Molecular Biology | Oncology
Abstract
Inflammatory breast cancer (IBC) is a rare and particularly lethal form of breast cancer. Despite aggressive therapeutic approaches, the 5-year survival rate is only 34%. As this disease is severely understudied, we have investigated the therapeutic potential of the novel hydroxamic acid-derived histone deacetylase inhibitor (HDACi), CG-1521 in comparison to a structurally similar compound, Trichostatin A (TSA) in two IBC cell lines: SUM149PT and SUM190PT. In these cells, CG-1521 and TSA induce dose- and time-dependent induction of cell cycle arrest and apoptosis regardless of the presence of 17β-estradiol (E2). Interestingly, the cell lines have considerably different sensitivities to these treatments despite their common disease origin.
Recommended Citation
Chatterjee, Namita, "Molecular actions of the novel histone deacetylase inhibitor CG-1521 in models of inflammatory breast cancer" (2014). Legacy Theses & Dissertations (2009 - 2024). 1101.
https://scholarsarchive.library.albany.edu/legacy-etd/1101
Included in
Biology Commons, Molecular Biology Commons, Oncology Commons