Dana-Farber Researchers Find Link Between Down Syndrome and Leukemia
The connection was made in mouse models.
People with Down syndrome have an increased risk for a variety of health problems, including heart defects, respiratory and hearing difficulties, and thyroid conditions. But they also have a heightened risk of developing acute lymphoblastic leukemia (ALL) during childhood. In fact, the risk is 20 times greater than that of the general population. And according to reps at Dana-Farber Cancer Institute, doctors have not been able to explain why. That is, until now. A team of Dana-Farber researchers has finally uncovered a connection between the two conditions.
In a new study published in the journal Nature Genetics, the researchers tracked the links of chromosomal abnormality in Down syndrome to the “cellular havoc” that occurs in ALL. “For 80 years, it hasn’t been clear why children with Down syndrome face a sharply elevated risk of ALL,” said the study’s lead author, Dr. Andrew Lane, of Dana-Farber’s Division of Hematologic Neoplasia. “Advances in technology – which make it possible to study blood cells and leukemias that model Down syndrome in the laboratory – have enabled us to make that link.”
According to a report released by Dana-Farber:
The syndrome occurs in people who have an extra copy of a single chromosome, known as chromosome 21. The addition may involve the entire chromosome or a portion of it.
To trace the link between Down syndrome and ALL – specifically, the most common form of the disease known as B cell ALL, or B-ALL – Lane, who is also a medical oncologist in the Dana-Farber/Brigham and Women’s Cancer Center Adult Stem Cell Transplantation Program, and his colleagues acquired a strain of mice that carry an extra copy of 31 genes found on chromosome 21 in humans.
“B-ALL occurs when the body produces too many immature B cells, which are a type of white blood cell that normally fights infections,” Lane says in the report. “When we tested the mice’s B cells in the laboratory, we found they were abnormal and grew uncontrollably – just as B cells from B-ALL patients do.”
The researchers then looked at the mice’s B cells to find the “molecular signature,” or the pattern of gene activity that distinguished them from normal B cells in mice. According to the report, the researchers found that in the abnormal cells, the group of proteins called PRC2 weren’t functioning. So, the researchers suggest that it’s the loss of PRC2 that was responsible for the B cells dividing and proliferating before they were fully mature.
The report says:
To confirm that a shutdown of PRC2 is critical to the formation of B-ALL in people with Down syndrome, Lane’s team focused on the genes controlled by PRC2. Using two sets of B-ALL cell samples – one from patients with Down syndrome, the other from patients without the syndrome – they measured the activity of thousands of different genes, looking for differences between the two sets. About 100 genes turned out to be much more active in the Down syndrome group, and all of them were under control of PRC2. When PRC2 is silenced – as it is in the B cells of Down syndrome patients – those 100 genes respond with a burst of activity, driving cell growth and division.
“We concluded that the extra copy of HMGN1 is important for turning off PRC2, and that, in turn, increases the cell proliferation,” Lane remarked. “This provides the long-sought after molecular link between Down syndrome and the development of B cell ALL.”
There are currently no drugs that target HMGN1, which researchers say could potentially “short-circuit the leukemia process in people with Down syndrome,” and so they are suggesting that drugs that switch on PRC2 could have an anti-leukemic effect in some of those people. “Work is under way to improve these drugs, known as histone demethylase inhibitors, so they can be tested in cell samples and animal models,” the report says.