Targeting Transcriptional Addiction For Cancer Therapy
Funder
National Health and Medical Research Council
Funding Amount
$128,224.00
Summary
.Tumours driven by the oncogene “Myc” are difficult to treat and an effective means to directly target Myc using small molecules has proven elusive. We have discovered that Myc-dependent tumours are dependent on their ability to globally amplify gene expression through a mechanism that involves the CDK9 enzyme and possibly other related enzymes. I will test the effectiveness of targeting CDK9 in a range of tumours with a Myc dependency, both alone and in combination with other small molecules.
The Function Of BHLH Factors In Adult Haemopoiseis
Funder
National Health and Medical Research Council
Funding Amount
$595,353.00
Summary
Understanding how genes control the behaviour of bone marrow stem cells is currently needed for improving recovery after chemotherapy or bone marrow transplantation and in the future, will aid the application of new stem cell-based therapies for human diseases such as leukaemia. This research will examine how 2 closely related genes control bone marrow stem cell growth and the decision between beocoming a red cell or a white cell.
Hemoglobin is the major protein in red blood cells and is essential for the transport of oxygen from the lungs to the tissues. The disorders of hemoglobin production are the commonest genetic diseases world-wide. These diseases can be markedly improved with elevation of the form of hemoglobin produced by the developing fetus, fetal hemoglobin. We have identified a key factor important for fetal gene expression. We will now determine whether manipulation of this factor can cure hemoglobin disorde ....Hemoglobin is the major protein in red blood cells and is essential for the transport of oxygen from the lungs to the tissues. The disorders of hemoglobin production are the commonest genetic diseases world-wide. These diseases can be markedly improved with elevation of the form of hemoglobin produced by the developing fetus, fetal hemoglobin. We have identified a key factor important for fetal gene expression. We will now determine whether manipulation of this factor can cure hemoglobin disorders.Read moreRead less
Identification Of Novel Mechanisms Governing Stage-specific Regulation Of The Human Globin Genes
Funder
National Health and Medical Research Council
Funding Amount
$577,889.00
Summary
Hemoglobin is the major protein in red blood cells and is essential for the transport of oxygen from the lungs to the tissues. The disorders of hemoglobin production are the commonest genetic diseases world-wide. These diseases can be markedly improved with elevation of the form of hemoglobin produced by the developing embryo, embryonic hemoglobin. We have identified a key factor important for fetal gene expression. Our goal is to translate these findings into therapies for the globin disorders.
Modelling Haematopoietic Disease And Leukocyte Function Using Zebrafish Models
Funder
National Health and Medical Research Council
Funding Amount
$686,656.00
Summary
Dr Lieschke studies white blood cell function and diseases. His biomedical research uses zebrafish animal models of human white blood cell diseases and he is an international expert on their blood and immune systems. His current research aims to understand what goes wrong in diseases when there are too many white blood cells (as in leukaemia), or too few (as in some hereditary diseases), and to develop new therapies for controlling inflammatory and infective diseases.
The Role Of Med12, A Subunit Of RNA Polymerase II Mediator, In Haemopoiesis
Funder
National Health and Medical Research Council
Funding Amount
$495,490.00
Summary
In a screen of zebrafish for mutations in blood cell development, we isolated a mutant called syrah. The mutation causing the blood defect was identified in a gene called med12, which encodes a component of the RNA transcription machinery in cells. To understand how this mutation causes a reduction in blood cells, we will identify the proteins that interact with the med12 protein. Understanding the pathway involved may lead to the discovery of new causes of human congenital blood diseases.