Document Type
Dissertation
Degree
Doctor of Philosophy (PhD)
Major/Program
Public Health
First Advisor's Name
Deodutta Roy
First Advisor's Committee Title
Committee Chair
Second Advisor's Name
Changwon Yoo
Third Advisor's Name
Quentin Felty
Fourth Advisor's Name
Nasar Ahmed
Keywords
Environmental exposure, pesticide, brain tumor, astrocytoma, glioblastoma, bioinformatics, gene networking, bayesian networking, meta-analysis
Date of Defense
11-14-2011
Abstract
The etiology of central nervous system tumors (CNSTs) is mainly unknown. Aside from extremely rare genetic conditions, such as neurofibromatosis and tuberous sclerosis, the only unequivocally identified risk factor is exposure to ionizing radiation, and this explains only a very small fraction of cases. Using meta-analysis, gene networking and bioinformatics methods, this dissertation explored the hypothesis that environmental exposures produce genetic and epigenetic alterations that may be involved in the etiology of CNSTs.
A meta-analysis of epidemiological studies of pesticides and pediatric brain tumors revealed a significantly increased risk of brain tumors among children whose mothers had farm-related exposures during pregnancy. A dose response was recognized when this risk estimate was compared to those for risk of brain tumors from maternal exposure to non-agricultural pesticides during pregnancy, and risk of brain tumors among children exposed to agricultural activities. Through meta-analysis of several microarray studies which compared normal tissue to astrocytomas, we were able to identify a list of 554 genes which were differentially expressed in the majority of astrocytomas. Many of these genes have in fact been implicated in development of astrocytoma, including EGFR, HIF-1α, c-Myc, WNT5A, and IDH3A. Reverse engineering of these 554 genes using Bayesian network analysis produced a gene network for each grade of astrocytoma (Grade I-IV), and ‘key genes’ within each grade were identified. Genes found to be most influential to development of the highest grade of astrocytoma, Glioblastoma multiforme (GBM) were: COL4A1, EGFR, BTF3, MPP2, RAB31, CDK4, CD99, ANXA2, TOP2A, and SERBP1. Lastly, bioinformatics analysis of environmental databases and curated published results on GBM was able to identify numerous potential pathways and gene-environment interactions that may play key roles in astrocytoma development.
Findings from this research have strong potential to advance our understanding of the etiology and susceptibility to CNSTs. Validation of our 'key genes' and pathways could potentially lead to useful tools for early detection and novel therapeutic options for these tumors.
Identifier
FI11120809
Recommended Citation
Kunkle, Brian W., "The Potential Role of Environmental Exposures and Genomic Signaling in Development of Central Nervous System Tumors" (2011). FIU Electronic Theses and Dissertations. 524.
https://digitalcommons.fiu.edu/etd/524
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