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Relapse in acute myeloid leukemia traced to rare stem cells

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Leukemia researchers led by John Dick, Ph.D., FRS, have traced the origins of relapse in acute myeloid leukemia (AML) to rare therapy-resistant leukemia stem cells that are already present at diagnosis and before chemotherapy begins.

They have also identified two distinct stem cell-like populations from which relapse can arise in different patients in this aggressive cancer that they previously showed starts in blood stem cells in the bone marrow.

The findings – published in Nature – provide significant insight into cell types fated to relapse and can help accelerate the quest for new, upfront therapies, said Dr. Dick, a senior scientist at Princess Margaret Cancer Centre, University Health Network, and professor in the Department of Molecular Genetics, University of Toronto. This study was primarily undertaken by post-doctoral fellow Liran Shlush and scientific associate Amanda Mitchell, Ph.D.

"For the first time, we have married together knowledge of stem cell biology and genetics – areas that historically have often been operating as separate camps – to identify mutations stem cells carry and how they are related to one another in AML," said Dr. Dick.

The researchers set out to solve the mystery of AML relapse by analyzing paired patient samples of blood taken at the initial clinic visit and blood taken post-treatment when disease recurred.

"First, we asked what are the similarities and differences between these samples. We carried out detailed genetic studies and used whole genome sequencing to look at every part of the DNA at diagnosis, and every part of the DNA at relapse," Dr. Dick said. "Next, we asked in which cells are genetic changes occurring."

The two-part approach netted a set of mutations seen only at relapse that enabled the team to sift and sort leukemic and normal stem cells using tools developed in the Dick lab a few years ago to zero in on specific cell types fated to relapse.

Today's findings augment recent research also published in Nature (Dec.7, 2016) detailing the team's development of a "stemness biomarker" – a 17-gene signature derived from leukemia stem cells that can predict at diagnosis which AML patients will respond to standard treatment.

"Our new findings add to that knowledge and we hope that we will soon have a new biomarker that will tell whether a patient will respond to standard chemotherapy, and then another to track patients in remission to identify those where treatment failed and the rare leukemia stem cells are coming back," Dr. Dick said. "These new kinds of biomarkers will lead to new kinds of clinical trials with targeted chemotherapy. Right now, everybody gets one size fits all because in AML we've never had any opportunity to identify patients upfront, only after they relapse.

"Now we have the first step to identify these patients at the outset and during remission."

Watch the video:
https://youtu.be/x5gF13nFlGY

Learn more:
http://www.uhn.ca/corporate/News/PressReleases/Pages/stem-cell_researchers_solve_mystery_relapse_acute_myeloid_leukemia.aspx
DOI:10.1038/nature22993