Abstract
Genetic or epigenetic loss of phosphatase and tensin homolog (PTEN) contributes to the initiation, progression and drug resistance of many human cancers. However, PTEN is strongly expressed in central nervous system (CNS) neurons, and inhibits their ability to survive and regenerate axons to restore functional connections after traumatic brain or spinal cord injury, stroke or neurodegenerative disease. This research developed genetic and epigenetic editing tools to restore expression of PTEN in cancer cells where the gene was transcriptionally repressed or mutated, and to silence PTEN expression in CNS neurons, with potential future applications for treatment of cancer and CNS regenerative failure.
Original language | English |
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Qualification | Doctor of Philosophy |
Awarding Institution |
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Thesis sponsors | |
Award date | 25 Oct 2018 |
DOIs | |
Publication status | Unpublished - 2018 |