Graduation Semester and Year
2007
Language
English
Document Type
Thesis
Degree Name
Master of Science in Biology
Department
Biology
First Advisor
Michael Roner
Abstract
Reovirus is a ubiquitous virus with demonstrated oncolytic properties. In this study, we investigate the pathways which reovirus produces a lytic infection in SV-40 transformed WI-38 cells and the noncytocidal infection of normal WI-38 cells using microarray technology. The analysis revealed that reovirus infection induced changes in 178 genes, of which 112 genes were up regulated and 66 genes down regulated. Of the 112 up regulated genes, 13 of the WI-38 2RA genes were shown to be involved in apoptosis or inhibition of cellular DNA synthesis. Of the 66 genes down regulated, seven of the WI-38 genes displayed effects involved in apoptosis or inhibition of cell cycle progression, suggesting that inhibition of these genes prevented death in these cells. Additionally, five of the 62 up regulated WI-38 genes were found to be involved in cell survival. Reovirus caused lysis of transformed cells by over inducing a multitude of cellular targets.
Disciplines
Biology | Life Sciences
License
This work is licensed under a Creative Commons Attribution-NonCommercial-Share Alike 4.0 International License.
Recommended Citation
Chung, Jung Hwa, "Cellular Targets Involved In Reovirus-induced Oncolysis Of RAs-transformed Cells" (2007). Biology Theses. 60.
https://mavmatrix.uta.edu/biology_theses/60
Comments
Degree granted by The University of Texas at Arlington