The bcl-2 gene is highly expressed in various human malignancies where it promotes tumor formation and contributes to drug-resistance by preventing tumor cells from undergoing programmed death. A growing body of research evidence indicates that preventing bcl-2 expression either kills tumor cells outright or sensitizes them to radiation and/or chemotherapeutic agents. We therefore intend to develop compounds, suitable for human use, that repress bcl-2 gene expression by selectively activating genomic imprinting mechanisms. Our ultimate objective is to develop a new class of pharmacotherapeutic agents for the treatment of solid tumors and hematological cancers. In the Phase I grant period, we will employ proprietary gene inactivation technology to prepare a series of chemical compounds which will then be tested in cell-based assays to determine their capacity to (1) repress bcl-2 gene transcription and reduce intracellular Bcl-2 protein levels, (2) inhibit tumor cell growth, and (3) potentiate the antitumor actions of conventional chemotherapeutic agents. Our overall goal in the Phase I grant period is to identify lead compounds for pre-IND safety and efficacy testing. ? ?
Showing the most recent 10 out of 18 publications
