test Browse by Author Names Browse by Titles of Works Browse by Subjects of Works Browse by Issue Dates of Works

Advanced Search
& Collections
Issue Date   
Sign on to:   
Receive email
My Account
authorized users
Edit Profile   
About T-Space   

T-Space at The University of Toronto Libraries >
School of Graduate Studies - Theses >
Master >

Please use this identifier to cite or link to this item: http://hdl.handle.net/1807/18851

Title: The Genetic Program of Myc-potentiated Apoptosis: Systems Development
Authors: Rust, Andrew
Advisor: Penn, Linda Z.
Department: Medical Biophysics
Keywords: Myc
Issue Date: 15-Feb-2010
Abstract: Myc is a powerful oncogene frequently deregulated in cancer yet deregulated Myc alone does not lead to cellular transformation due to the intrinsic safety mechanism of deregulated Myc potentiating apoptosis. The mechanism by which Myc potentiates apoptosis remains unclear, however, because the regions of Myc essential for apoptosis are also required for Myc to function as a regulator of gene transcription, it is thought that Myc’s role in apoptosis is a function of its regulation of an apoptotic genetic program. We hypothesize that under apoptotic conditions, Myc differentially binds and/or regulates a specific cohort of genes to potentiate apoptosis. The foremost approach to addressing this hypothesis is the employment of ChIP-chip coupled with expression microarray analyses. Here, using the MCF10A breast epithelial and SHEP neuroblastoma cell lines, we developed and characterized two independent human systems for subsequent ChIP-chip and expression array analyses to elucidate the genetic program of Myc-potentiated apoptosis.
URI: http://hdl.handle.net/1807/18851
Appears in Collections:Master
Department of Medical Biophysics - Master theses

Files in This Item:

File Description SizeFormat
Rust_Andrew_C_200911_MSc_thesis.pdf1.3 MBAdobe PDF

This item is licensed under a Creative Commons License
Creative Commons

Items in T-Space are protected by copyright, with all rights reserved, unless otherwise indicated.