I have been working for Temple University, Information Technology Services for the past 13 years and have been supporting SHRO Institute for all their technological needs.
I am originally from Nigeria where I had my first Bachelor Degree in Microbiology from the University of Lagos. In 1997, I relocated to United States through diversity visa lottery with my family. Upon arrival to the US, I had my second Bachelor’s degree in Computer Science with minor in Mathematics from Drexel University, PA. After working for a brief period in New Jersey, I joined Temple University ITS and while working at Temple University I obtained my second degree, Masters in Health informatics from Temple University. In 2014, I obtained my PhD in Bioinformatics from Temple University and University of Siena with Dr. Giordano. In a way of giving back to the community, I offer to teach a non-credit course an evening class, Introduction to Personal Computer for PASCEP, Temple University Community Relation for the past few years.
For the past several years I have devoted my research to pathogenic infectious agents that contribute to disease in humans. I studied Schistosomiasis that causes liver and bladder cancers, and may affect the eyes too. Later I focused on HIV studying the different sub types and determining the virus effect on efficacy of children vaccines. This consortium work led to setting up of HIV antiviral therapy and vaccination standards in children. Adults with HIV infection develop dementia, later called HIV dementia. I studied the pathogenic events involved in the disease.
This led to the revelation that some viral particles do cross the blood/brain barrier leading to production of inflammatory factors that have been associated with infectious agents and cancer. These findings led to my interest in studying the role of infectious agents such as HIV in initiation of cancer. The accepted dogma then, and in some cancers that are caused by infectious agents was that one virus or bacteria was involved. My contention was that more than one agent was involved and that they interact in different levels to initiate the disease.
Studying Ocular Surface Squamous Neoplasia (OSSN), I showed that contrary to the belief then that only HPV was involved; EBV, KSHV were also involved, and possible other pathogens that have not been identified. I have since identified other pathogenic sequences in the OSSN tissues. Thus, our work has shown the association of the pathogenic viruses with ocular cancers that will have an impact on translational medicine. With the latest technology we are beginning to find that other pathogens may also be involved, and the interaction of these pathogenic oncogenes as they usurp the pathways in cell cycle is of considerable significance to us.