Investigating factors that may cause genetic changes in leukaemia
Under the supervision of Dr Steven Lane and Professor Geoff Hill at the QIMR Berghofer Medical Research Institute, PhD student Therese Vu is investigating the role of a gene, DNMT3A, that may play a role in transforming a blood disorder into acute myeloid leukaemia (AML).
Mutations of DNMT3A exist in up to 20 per cent of AML cases, however it is unknown what role the enzyme plays in either the development or sustenance of the cancer.
A better understanding of the gene’s role in myeloproliferative neoplasms (MPN) and the genetic pathways that progress MPN into AML may lead to new ways to intervene early and prevent the development of AML in some patients.
“We don’t understand a lot about the function of DNMT3A in MPN, so I’m investigating its role in normal blood formation as well as how mutations in the gene may lead to disease,” said Therese.
“I’m also using laboratory models to see if we can accurately imitate the conditions seen in patients with blood disorders, and use these to test targeted treatments to try and restore normal gene expression and maybe sensitise malignant cells to chemotherapy.”