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.

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