Theses and Dissertations
Date of Award
5-2020
Document Type
Thesis
Degree Name
Master of Science (MS)
Department
Biology
First Advisor
Dr. Megan Keniry
Second Advisor
Dr. Scott Gunn
Third Advisor
Dr. Robert Gilkerson
Abstract
The Phosphatidylinositol 3 Kinase (PI3K) pathway is an essential intracellular signaling pathway that regulates cellular growth, survival, and fate. Canonically, the activation of this pathway removes forkhead box subfamily O transcription factors (FOXO -1, -3, and -4) from the nucleus. However, in cancer cells such as glioblastoma multiforme, FOXO factors are at least in part nuclear despite the activation of the PI3K pathway. Previous research indicated that FOXO3 localization was not affected when the pathway was inhibited in breast cancer cells, which challenged the conventional paradigms for FOXO factor regulation. Therefore, we were interested in investigating the nuclear localization of FOXO transcription factors in additional cancer settings such as glioblastoma. By inhibiting PI3K and other pathways linked to FOXO factors, we examined their effects on FOXO transcription factor localization. We found that FOXO factors bypass the regulation by PI3K in order to be localized in the nucleus in glioblastoma cells.
Recommended Citation
Hinojosa, Leetoria, "Investigating the Localization of FOXO Transcription Factors in Glioblastoma" (2020). Theses and Dissertations. 678.
https://scholarworks.utrgv.edu/etd/678
Comments
Copyright 2020 Leetoria Hinojosa. All Rights Reserved.
https://go.openathens.net/redirector/utrgv.edu?url=https://www.proquest.com/dissertations-theses/investigating-localization-foxo-transcription/docview/2454633897/se-2?accountid=7119