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Opening the door to the cause of myeloid leukemia: Finding the targets of common mutation

Date:
July 23, 2015
Source:
University of Birmingham
Summary:
A breakthrough in understanding how mutated genes in leukemia reprogram blood stem cells and send them spiraling out of control has been made by a team of scientists.
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Researchers at the University of Birmingham have made a breakthrough in understanding how mutated genes in leukemia reprogram blood stem cells and send them spiralling out of control.

The findings help to explain the early development of leukemia, representing the essential first step to developing new treatments for patients based on these findings.

A study, published in Cell Reports by Professors Peter Cockerill and Constanze Bonifer, investigated the role of one specific mutation in the FLT3 gene found in acute myeloid leukemia (AML).

AML is diagnosed in around 2,400 people in the UK each year. While younger patients have a better prognosis, overall survival rates are very poor and new treatments are needed.

FLT3 is a protein that normally makes sure that blood stem cells produce just the right number of blood cells every day. When it gets mutated it sends the wrong signals and keeps the stem cells expanding out of control, swamping the body with abnormal blood cells.

Professor Peter Cockerill, of the University of Birmingham, explained: "We found that the mutated FLT3 protein always sends the same signals to the same set of genes in all AML patients that have this mutation. By finding out which signals and genes are the targets, we now have new targets that will allow us to attack this pathway."

The team found that the mutated FLT3 protein used one specific signalling pathway inside the cell to activate over 1,000 different targets within the DNA, leading to the abnormal activation of over 100 genes in patients who have this mutation. Many of these genes were already known to contribute to cancer by sending growth signals.

The project was funded by Leukemia and Lymphoma Research. Dr Matt Kaiser, Head of Research at Leukemia & Lymphoma Research, said: "Unfortunately there have been no significant improvements in survival rates for acute myeloid leukemia in the last two decades. These findings provide renewed hope for developing new treatments for this aggressive type of leukemia."


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Materials provided by University of Birmingham. Note: Content may be edited for style and length.


Journal Reference:

  1. Peter Cockerill and Constanze Bonifer et al. Chronic FLT3-ITD Signaling in Acute Myeloid Leukemia Is Connected to a Specific Chromatin Signature. Cell Reports, July 2015 DOI: 10.1016/j.celrep.2015.06.069

Cite This Page:

University of Birmingham. "Opening the door to the cause of myeloid leukemia: Finding the targets of common mutation." ScienceDaily. ScienceDaily, 23 July 2015. <www.sciencedaily.com/releases/2015/07/150723125240.htm>.
University of Birmingham. (2015, July 23). Opening the door to the cause of myeloid leukemia: Finding the targets of common mutation. ScienceDaily. Retrieved May 23, 2017 from www.sciencedaily.com/releases/2015/07/150723125240.htm
University of Birmingham. "Opening the door to the cause of myeloid leukemia: Finding the targets of common mutation." ScienceDaily. www.sciencedaily.com/releases/2015/07/150723125240.htm (accessed May 23, 2017).

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