New clue to fighting acute myeloid leukemia found

AML usually originates from the bone marrow, where blood cells are produced. It is characterized by an overproduction of impaired white blood cells. The differentiation of immature white blood cell precursors into functional white blood cells is an essential process mediating the body's immunity. The research team found that an enzyme, GCN5, is able to inactivate a protein called C/EBPa in myeloid precursor cells. This prevents immature myeloid white blood cells from maturing into granulocytes -- which make up about 70 per cent of white blood cells in the body. As a result, healthy white blood cells formation is disrupted.

The team, which includes Professor Daniel Tenen, Director of CSI Singapore, Ms Kwok Hui Si, PhD student at the Institute, as well as Dr Deepak Bararia, a former Postdoctoral Fellow at the Institute, discovered that the inactivation of the C/EBPa protein is carried out by acetylation, which is a process by which GCN5 adds an acetyl group onto C/EBPa reducing the ability of C/EBPa to bind to DNA and modulating its transcriptional activity in the cell.

The findings of the study were published in the journal Nature Communications on 24 March 2016.

Identification of this molecular pathway provides clues towards targeting the GCN5-mediated acetylation of C/EBPa in the treatment of leukemia.

Prof Tenen said, "As AML is a fast-growing cancer, timely treatment soon after diagnosis could increase patients' chances of survival. The current main treatment strategy for AML is cytotoxic chemotherapy. Our research results form the basis of an alternative therapeutic strategy that could potentially reduce remission risks and improve cure rates. Moving forward, the team is looking into designing effective GCN5 inhibitors for therapeutic purposes by studying GCN5 in AML further in depth."